geneid | 1182 |
---|---|
ensemblid | ENSG00000109572.16 |
hgncid | 2021 |
symbol | CLCN3 |
name | chloride voltage-gated channel 3 |
refseq_nuc | NM_001829.4 |
refseq_prot | NP_001820.2 |
ensembl_nuc | ENST00000513761.6 |
ensembl_prot | ENSP00000424603.1 |
mane_status | MANE Select |
chr | chr4 |
start | 169620578 |
end | 169723673 |
strand | + |
ver | v1.2 |
region | chr4:169620578-169723673 |
region5000 | chr4:169615578-169728673 |
regionname0 | CLCN3_chr4_169620578_169723673 |
regionname5000 | CLCN3_chr4_169615578_169728673 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 818 | 287 | 95 | 50 | 88 | 16 | 36 | 62 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0002 | 0/0 | 818 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2457 | 167 | 54 | 32 | 44 | 9 | 26 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
c0002 | 0/0 | 2457 | 66 | 10 | 12 | 35 | 4 | 5 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
c0003 | 0/0 | 2457 | 50 | 29 | 5 | 8 | 3 | 5 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
c0004 | 0/0 | 2457 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
c0005 | 0/0 | 2457 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
c0006 | 0/0 | 2457 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
c0007 | 0/0 | 2457 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
c0008 | 0/0 | 2457 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 4175 | 86 | 13 | 21 | 39 | 2 | 11 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0002 | 0/0 | 4179 | 49 | 1 | 7 | 33 | 3 | 5 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0003 | 0/0 | 4178 | 24 | 8 | 2 | 7 | 3 | 4 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0004 | 0/0 | 4178 | 15 | 13 | 2 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0005 | 1/0 | 4179 | 14 | 12 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0006 | 0/0 | 4180 | 8 | 8 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0007 | 0/1 | 4195 | 8 | 2 | 1 | 0 | 3 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0008 | 0/0 | 4177 | 6 | 4 | 1 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0009 | 0/0 | 4176 | 5 | 5 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0010 | 0/0 | 4193 | 5 | 0 | 3 | 0 | 0 | 2 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0011 | 0/0 | 4168 | 4 | 4 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0012 | 0/0 | 4185 | 4 | 4 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0013 | 0/0 | 4189 | 4 | 0 | 1 | 1 | 1 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0014 | 0/0 | 4191 | 4 | 0 | 2 | 0 | 1 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0015 | 0/0 | 4176 | 3 | 3 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0016 | 0/0 | 4197 | 3 | 0 | 0 | 1 | 0 | 2 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0017 | 0/0 | 4179 | 3 | 0 | 2 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0018 | 0/0 | 4175 | 2 | 0 | 1 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0019 | 0/0 | 4174 | 2 | 0 | 2 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0020 | 0/0 | 4178 | 2 | 2 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0021 | 0/0 | 4177 | 2 | 0 | 0 | 2 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0022 | 0/0 | 4180 | 2 | 2 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0023 | 0/0 | 4180 | 2 | 1 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0024 | 0/0 | 4199 | 2 | 0 | 0 | 0 | 0 | 2 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0025 | 0/0 | 4180 | 2 | 2 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0026 | 0/0 | 4175 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0027 | 0/0 | 4192 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0028 | 0/0 | 4200 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0029 | 0/0 | 4164 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0030 | 0/0 | 4175 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0031 | 0/0 | 4175 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0032 | 0/0 | 4175 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0033 | 0/0 | 4179 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0034 | 0/0 | 4179 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0035 | 0/0 | 4178 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0036 | 0/0 | 4179 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0037 | 0/0 | 4182 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0038 | 0/0 | 4181 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0039 | 0/0 | 4180 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0040 | 0/0 | 4181 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0041 | 0/0 | 4181 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0042 | 0/0 | 4181 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0043 | 0/0 | 4182 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0044 | 0/0 | 4189 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0045 | 0/0 | 4191 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0046 | 0/0 | 4199 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0047 | 0/0 | 4205 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0048 | 0/0 | 4207 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0049 | 0/0 | 4178 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0050 | 0/0 | 4179 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0051 | 0/0 | 4177 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
t0052 | 0/0 | 4194 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0103 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0251 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2457 | 167 | 54 | 32 | 44 | 9 | 26 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0002 | 0/0 | 2457 | 66 | 10 | 12 | 35 | 4 | 5 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0003 | 0/0 | 2457 | 50 | 29 | 5 | 8 | 3 | 5 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0004 | 0/0 | 2457 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0006 | 0/0 | 2457 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0007 | 0/0 | 2457 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0008 | 0/0 | 2457 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0002c0005 | 0/0 | 2457 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6631 | 85 | 13 | 20 | 39 | 2 | 11 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0001t0005 | 1/0 | 6635 | 13 | 11 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0001t0006 | 0/0 | 6636 | 8 | 8 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0001t0007 | 0/1 | 6651 | 8 | 2 | 1 | 0 | 3 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0001t0010 | 0/0 | 6649 | 5 | 0 | 3 | 0 | 0 | 2 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0001t0011 | 0/0 | 6624 | 4 | 4 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0001t0012 | 0/0 | 6641 | 3 | 3 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0001t0013 | 0/0 | 6645 | 4 | 0 | 1 | 1 | 1 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0001t0014 | 0/0 | 6647 | 4 | 0 | 2 | 0 | 1 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0001t0015 | 0/0 | 6632 | 3 | 3 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0001t0016 | 0/0 | 6653 | 3 | 0 | 0 | 1 | 0 | 2 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0001t0018 | 0/0 | 6631 | 2 | 0 | 1 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0001t0019 | 0/0 | 6630 | 2 | 0 | 2 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0001t0021 | 0/0 | 6633 | 2 | 0 | 0 | 2 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0001t0024 | 0/0 | 6655 | 2 | 0 | 0 | 0 | 0 | 2 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0001t0025 | 0/0 | 6636 | 2 | 2 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0001t0026 | 0/0 | 6631 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0001t0027 | 0/0 | 6648 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0001t0028 | 0/0 | 6656 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0001t0030 | 0/0 | 6631 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0001t0031 | 0/0 | 6631 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0001t0032 | 0/0 | 6631 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0001t0033 | 0/0 | 6635 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0001t0034 | 0/0 | 6635 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0001t0035 | 0/0 | 6634 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0001t0038 | 0/0 | 6637 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0001t0042 | 0/0 | 6637 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0001t0043 | 0/0 | 6638 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0001t0044 | 0/0 | 6645 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0001t0045 | 0/0 | 6647 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0001t0047 | 0/0 | 6661 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0001t0048 | 0/0 | 6663 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0001t0052 | 0/0 | 6650 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0002t0002 | 0/0 | 6635 | 48 | 0 | 7 | 33 | 3 | 5 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0002t0008 | 0/0 | 6633 | 6 | 4 | 1 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0002t0009 | 0/0 | 6632 | 5 | 5 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0002t0017 | 0/0 | 6635 | 3 | 0 | 2 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0002t0036 | 0/0 | 6635 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0002t0041 | 0/0 | 6637 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0002t0050 | 0/0 | 6635 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0002t0051 | 0/0 | 6633 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0003t0003 | 0/0 | 6634 | 24 | 8 | 2 | 7 | 3 | 4 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0003t0004 | 0/0 | 6634 | 15 | 13 | 2 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0003t0020 | 0/0 | 6634 | 2 | 2 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0003t0022 | 0/0 | 6636 | 2 | 2 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0003t0023 | 0/0 | 6636 | 2 | 1 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0003t0029 | 0/0 | 6620 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0003t0037 | 0/0 | 6638 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0003t0039 | 0/0 | 6636 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0003t0040 | 0/0 | 6637 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0003t0049 | 0/0 | 6634 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0004t0002 | 0/0 | 6635 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0006t0046 | 0/0 | 6655 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0007t0001 | 0/0 | 6631 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0001c0008t0005 | 0/0 | 6635 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
a0002c0005t0012 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | copy fasta | chr4 | 169615578 | 169728673 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0005g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0005g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0005g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0005g0251 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0005g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0005g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0005g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0005g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0005g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0005g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0005g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0006g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0006g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0006g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0006g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0006g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0006g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0006g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0006g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0007g0103 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0007g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0007g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0007g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0007g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0007g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0007g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0007g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0010g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0010g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0010g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0010g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0010g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0011g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0011g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0011g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0011g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0012g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0012g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0012g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0013g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0013g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0013g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0013g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0014g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0014g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0014g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0014g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0015g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0015g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0015g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0016g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0016g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0016g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0018g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0018g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0019g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0019g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0021g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0021g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0024g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0024g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0025g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0026g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0027g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0028g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0030g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0031g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0032g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0033g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0034g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0035g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0038g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0042g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0043g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0044g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0045g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0047g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0048g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0001t0052g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0008g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0008g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0008g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0008g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0008g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0008g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0009g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0009g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0009g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0009g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0009g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0017g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0017g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0036g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0041g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0050g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0002t0051g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0003g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0003g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0003g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0003g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0003g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0003g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0003g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0004g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0004g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0020g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0020g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0022g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0022g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0023g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0023g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0029g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0037g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0039g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0040g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0003t0049g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0004t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0006t0046g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0007t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0001c0008t0005g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
a0002c0005t0012g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0007 | g0215 | EUR | GBR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG00099 | hp2 | a0001 | c0001 | t0032 | g0185 | EUR | GBR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG00140 | hp1 | a0001 | c0001 | t0007 | g0227 | EUR | GBR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG00140 | hp2 | a0001 | c0002 | t0002 | g0079 | EUR | GBR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG00280 | hp1 | a0001 | c0002 | t0002 | g0032 | EUR | FIN | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0129 | EUR | FIN | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG00323 | hp1 | a0001 | c0001 | t0018 | g0170 | EUR | FIN | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG00323 | hp2 | a0001 | c0001 | t0007 | g0217 | EUR | FIN | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG00558 | hp1 | a0001 | c0002 | t0002 | g0090 | EAS | CHS | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG00597 | hp1 | a0001 | c0002 | t0002 | g0075 | EAS | CHS | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG00609 | hp1 | a0001 | c0002 | t0002 | g0071 | EAS | CHS | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG00621 | hp2 | a0001 | c0002 | t0002 | g0092 | EAS | CHS | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG00639 | hp2 | a0001 | c0003 | t0004 | g0051 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG00733 | hp1 | a0001 | c0007 | t0001 | g0162 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG00733 | hp2 | a0001 | c0001 | t0007 | g0214 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG00738 | hp1 | a0001 | c0001 | t0010 | g0236 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01069 | hp2 | a0001 | c0002 | t0050 | g0104 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01099 | hp1 | a0001 | c0001 | t0014 | g0229 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01106 | hp2 | a0001 | c0002 | t0002 | g0057 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01109 | hp1 | a0001 | c0001 | t0005 | g0253 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01109 | hp2 | a0001 | c0001 | t0028 | g0221 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01168 | hp2 | a0001 | c0001 | t0010 | g0238 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01175 | hp2 | a0001 | c0003 | t0004 | g0037 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01192 | hp2 | a0001 | c0002 | t0002 | g0083 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01243 | hp1 | a0001 | c0001 | t0014 | g0230 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01243 | hp2 | a0001 | c0002 | t0002 | g0082 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01255 | hp1 | a0001 | c0001 | t0010 | g0216 | AMR | CLM | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01255 | hp2 | a0001 | c0002 | t0002 | g0054 | AMR | CLM | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01257 | hp1 | a0001 | c0002 | t0017 | g0005 | AMR | CLM | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01258 | hp1 | a0001 | c0001 | t0019 | g0007 | AMR | CLM | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01258 | hp2 | a0001 | c0002 | t0017 | g0005 | AMR | CLM | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01261 | hp1 | a0001 | c0001 | t0018 | g0172 | AMR | CLM | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01261 | hp2 | a0001 | c0002 | t0041 | g0100 | AMR | CLM | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01346 | hp1 | a0001 | c0003 | t0003 | g0020 | AMR | CLM | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01358 | hp1 | a0001 | c0003 | t0023 | g0038 | AMR | CLM | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01433 | hp2 | a0001 | c0001 | t0013 | g0233 | AMR | CLM | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01496 | hp1 | a0001 | c0002 | t0008 | g0106 | AMR | CLM | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01496 | hp2 | a0001 | c0001 | t0019 | g0124 | AMR | CLM | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01516 | hp1 | a0001 | c0002 | t0017 | g0157 | EUR | IBS | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01516 | hp2 | a0001 | c0003 | t0003 | g0003 | EUR | IBS | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01517 | hp1 | a0001 | c0003 | t0003 | g0003 | EUR | IBS | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01517 | hp2 | a0001 | c0001 | t0014 | g0231 | EUR | IBS | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01884 | hp1 | a0001 | c0001 | t0006 | g0200 | AFR | ACB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01884 | hp2 | a0001 | c0003 | t0029 | g0047 | AFR | ACB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01978 | hp1 | a0001 | c0002 | t0002 | g0064 | AMR | PEL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01981 | hp1 | a0001 | c0003 | t0003 | g0027 | AMR | PEL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG01981 | hp2 | a0001 | c0002 | t0002 | g0085 | AMR | PEL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02027 | hp1 | a0001 | c0002 | t0002 | g0107 | EAS | KHV | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02040 | hp2 | a0001 | c0001 | t0016 | g0219 | EAS | KHV | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02055 | hp1 | a0001 | c0008 | t0005 | g0243 | AFR | ACB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02055 | hp2 | a0001 | c0003 | t0003 | g0029 | AFR | ACB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02129 | hp2 | a0001 | c0002 | t0002 | g0068 | EAS | KHV | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02132 | hp2 | a0001 | c0003 | t0003 | g0019 | EAS | KHV | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02135 | hp2 | a0001 | c0002 | t0002 | g0081 | EAS | KHV | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02145 | hp2 | a0001 | c0003 | t0004 | g0050 | AFR | ACB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CDX | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02155 | hp2 | a0001 | c0002 | t0036 | g0095 | EAS | CDX | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02257 | hp2 | a0001 | c0001 | t0007 | g0213 | AFR | ACB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02258 | hp1 | a0001 | c0001 | t0005 | g0249 | AFR | ACB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02258 | hp2 | a0001 | c0001 | t0030 | g0245 | AFR | ACB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02273 | hp1 | a0001 | c0002 | t0002 | g0084 | AMR | PEL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02280 | hp1 | a0001 | c0003 | t0040 | g0278 | AFR | ACB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02280 | hp2 | a0001 | c0003 | t0003 | g0022 | AFR | ACB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02451 | hp1 | a0001 | c0003 | t0004 | g0042 | AFR | ACB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02451 | hp2 | a0001 | c0002 | t0009 | g0053 | AFR | ACB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02572 | hp1 | a0001 | c0001 | t0011 | g0192 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02572 | hp2 | a0001 | c0001 | t0006 | g0199 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02602 | hp1 | a0001 | c0001 | t0016 | g0211 | SAS | PJL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02602 | hp2 | a0001 | c0001 | t0043 | g0260 | SAS | PJL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02615 | hp1 | a0001 | c0001 | t0006 | g0201 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02615 | hp2 | a0001 | c0001 | t0015 | g0195 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02622 | hp2 | a0001 | c0001 | t0005 | g0256 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02630 | hp1 | a0001 | c0001 | t0015 | g0190 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02647 | hp1 | a0001 | c0001 | t0005 | g0257 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02647 | hp2 | a0001 | c0001 | t0006 | g0267 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02683 | hp1 | a0001 | c0001 | t0007 | g0212 | SAS | PJL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02698 | hp2 | a0001 | c0001 | t0044 | g0232 | SAS | PJL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02717 | hp1 | a0001 | c0002 | t0008 | g0066 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02717 | hp2 | a0001 | c0003 | t0004 | g0041 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02723 | hp1 | a0001 | c0003 | t0023 | g0035 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02723 | hp2 | a0001 | c0003 | t0022 | g0208 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02735 | hp1 | a0001 | c0003 | t0003 | g0152 | SAS | PJL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02735 | hp2 | a0001 | c0001 | t0014 | g0234 | SAS | PJL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02738 | hp1 | a0001 | c0002 | t0002 | g0109 | SAS | PJL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02738 | hp2 | a0001 | c0001 | t0010 | g0209 | SAS | PJL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02809 | hp1 | a0001 | c0001 | t0005 | g0258 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02809 | hp2 | a0001 | c0002 | t0051 | g0031 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02818 | hp2 | a0001 | c0001 | t0011 | g0193 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02886 | hp1 | a0001 | c0003 | t0003 | g0017 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02886 | hp2 | a0001 | c0003 | t0020 | g0183 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02895 | hp1 | a0001 | c0001 | t0005 | g0252 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02895 | hp2 | a0001 | c0001 | t0005 | g0255 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02896 | hp1 | a0001 | c0001 | t0052 | g0030 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02896 | hp2 | a0001 | c0003 | t0003 | g0001 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02897 | hp1 | a0001 | c0003 | t0003 | g0001 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02897 | hp2 | a0001 | c0001 | t0005 | g0254 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02922 | hp1 | a0001 | c0001 | t0015 | g0196 | AFR | ESN | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02922 | hp2 | a0001 | c0001 | t0006 | g0203 | AFR | ESN | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02965 | hp1 | a0001 | c0001 | t0005 | g0250 | AFR | ESN | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02965 | hp2 | a0001 | c0002 | t0008 | g0205 | AFR | ESN | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02970 | hp1 | a0001 | c0003 | t0037 | g0040 | AFR | ESN | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02970 | hp2 | a0001 | c0001 | t0035 | g0014 | AFR | ESN | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02976 | hp1 | a0001 | c0002 | t0009 | g0096 | AFR | ESN | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02976 | hp2 | a0001 | c0001 | t0025 | g0002 | AFR | ESN | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG03041 | hp2 | a0001 | c0003 | t0022 | g0207 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG03098 | hp1 | a0001 | c0003 | t0003 | g0016 | AFR | MSL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG03098 | hp2 | a0001 | c0003 | t0004 | g0046 | AFR | MSL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG03130 | hp2 | a0001 | c0003 | t0004 | g0043 | AFR | ESN | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG03139 | hp1 | a0001 | c0003 | t0003 | g0277 | AFR | ESN | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG03139 | hp2 | a0001 | c0003 | t0004 | g0049 | AFR | ESN | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG03195 | hp1 | a0001 | c0001 | t0038 | g0248 | AFR | ESN | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG03195 | hp2 | a0001 | c0003 | t0004 | g0039 | AFR | ESN | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG03225 | hp1 | a0001 | c0001 | t0005 | g0247 | AFR | MSL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG03225 | hp2 | a0001 | c0002 | t0009 | g0099 | AFR | MSL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | MSL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG03453 | hp2 | a0001 | c0001 | t0005 | g0246 | AFR | MSL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG03486 | hp1 | a0001 | c0004 | t0002 | g0065 | AFR | MSL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG03486 | hp2 | a0001 | c0003 | t0004 | g0044 | AFR | MSL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG03490 | hp1 | a0001 | c0001 | t0047 | g0210 | SAS | PJL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG03490 | hp2 | a0001 | c0002 | t0002 | g0055 | SAS | PJL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG03491 | hp1 | a0001 | c0001 | t0013 | g0237 | SAS | PJL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG03492 | hp2 | a0001 | c0002 | t0002 | g0063 | SAS | PJL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ESN | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG03516 | hp2 | a0001 | c0003 | t0004 | g0036 | AFR | ESN | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG03540 | hp1 | a0001 | c0001 | t0012 | g0264 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG03540 | hp2 | a0001 | c0001 | t0005 | g0244 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG03579 | hp2 | a0001 | c0001 | t0045 | g0280 | AFR | MSL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG03654 | hp2 | a0001 | c0002 | t0002 | g0102 | SAS | PJL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG03688 | hp1 | a0001 | c0001 | t0016 | g0226 | SAS | STU | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | STU | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG03704 | hp1 | a0001 | c0001 | t0048 | g0225 | SAS | PJL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG03704 | hp2 | a0001 | c0003 | t0003 | g0269 | SAS | PJL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG03831 | hp1 | a0001 | c0001 | t0024 | g0218 | SAS | BEB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | BEB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | BEB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG03834 | hp2 | a0001 | c0001 | t0010 | g0224 | SAS | BEB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG03927 | hp1 | a0001 | c0001 | t0027 | g0223 | SAS | BEB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG03927 | hp2 | a0001 | c0003 | t0003 | g0272 | SAS | BEB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG04115 | hp2 | a0001 | c0001 | t0024 | g0222 | SAS | STU | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | STU | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG04204 | hp2 | a0001 | c0003 | t0003 | g0271 | SAS | STU | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG04228 | hp1 | a0001 | c0001 | t0031 | g0242 | SAS | STU | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG04228 | hp2 | a0001 | c0002 | t0002 | g0108 | SAS | STU | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA18522 | hp1 | a0001 | c0001 | t0011 | g0194 | AFR | YRI | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA18522 | hp2 | a0001 | c0001 | t0034 | g0241 | AFR | YRI | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA18612 | hp2 | a0001 | c0002 | t0002 | g0070 | EAS | CHB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA18747 | hp1 | a0001 | c0002 | t0002 | g0088 | EAS | CHB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | CHB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA18906 | hp1 | a0001 | c0001 | t0012 | g0262 | AFR | YRI | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA18906 | hp2 | a0001 | c0001 | t0006 | g0197 | AFR | YRI | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA18940 | hp1 | a0001 | c0003 | t0039 | g0015 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA18940 | hp2 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA18943 | hp2 | a0001 | c0002 | t0008 | g0086 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA18947 | hp2 | a0001 | c0002 | t0002 | g0080 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA18952 | hp2 | a0001 | c0002 | t0002 | g0073 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA18956 | hp2 | a0001 | c0002 | t0002 | g0089 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA18965 | hp2 | a0001 | c0002 | t0002 | g0101 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA18970 | hp1 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA18972 | hp1 | a0001 | c0002 | t0002 | g0087 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA18974 | hp1 | a0001 | c0006 | t0046 | g0220 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA18974 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA18981 | hp1 | a0001 | c0002 | t0002 | g0072 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA18982 | hp1 | a0001 | c0003 | t0003 | g0023 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA18984 | hp1 | a0001 | c0002 | t0002 | g0067 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA18984 | hp2 | a0001 | c0003 | t0003 | g0013 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA18986 | hp2 | a0001 | c0002 | t0002 | g0076 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA18989 | hp1 | a0001 | c0002 | t0002 | g0058 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA18989 | hp2 | a0001 | c0003 | t0003 | g0026 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA18994 | hp2 | a0001 | c0003 | t0003 | g0025 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA19003 | hp2 | a0001 | c0002 | t0002 | g0105 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA19007 | hp1 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA19009 | hp2 | a0001 | c0003 | t0003 | g0021 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA19012 | hp1 | a0001 | c0002 | t0002 | g0078 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA19030 | hp1 | a0001 | c0003 | t0020 | g0184 | AFR | LWK | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA19030 | hp2 | a0001 | c0002 | t0008 | g0204 | AFR | LWK | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA19043 | hp1 | a0001 | c0002 | t0008 | g0206 | AFR | LWK | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA19043 | hp2 | a0002 | c0005 | t0012 | g0263 | AFR | LWK | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA19058 | hp2 | a0001 | c0001 | t0013 | g0008 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA19065 | hp2 | a0001 | c0002 | t0002 | g0091 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA19066 | hp1 | a0001 | c0002 | t0002 | g0056 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA19066 | hp2 | a0001 | c0003 | t0003 | g0024 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA19068 | hp1 | a0001 | c0001 | t0021 | g0008 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA19074 | hp1 | a0001 | c0002 | t0002 | g0094 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA19074 | hp2 | a0001 | c0001 | t0026 | g0132 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA19078 | hp2 | a0001 | c0002 | t0002 | g0060 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA19083 | hp2 | a0001 | c0002 | t0002 | g0069 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA19084 | hp1 | a0001 | c0001 | t0021 | g0228 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA19087 | hp2 | a0001 | c0002 | t0002 | g0093 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA19089 | hp1 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA19091 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA19240 | hp1 | a0001 | c0002 | t0009 | g0098 | AFR | YRI | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA19240 | hp2 | a0001 | c0001 | t0006 | g0198 | AFR | YRI | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA20129 | hp1 | a0001 | c0003 | t0003 | g0018 | AFR | ASW | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA20129 | hp2 | a0001 | c0001 | t0006 | g0202 | AFR | ASW | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA20752 | hp1 | a0001 | c0001 | t0013 | g0261 | EUR | TSI | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA20752 | hp2 | a0001 | c0003 | t0003 | g0028 | EUR | TSI | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA20805 | hp1 | a0001 | c0002 | t0002 | g0059 | EUR | TSI | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0114 | EUR | TSI | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | GIH | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA20905 | hp2 | a0001 | c0003 | t0049 | g0270 | SAS | GIH | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02109 | hp2 | a0001 | c0002 | t0009 | g0097 | AFR | ACB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02486 | hp1 | a0001 | c0003 | t0004 | g0034 | AFR | ACB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02486 | hp2 | a0001 | c0001 | t0012 | g0259 | AFR | ACB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02559 | hp1 | a0001 | c0003 | t0004 | g0048 | AFR | ACB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG02559 | hp2 | a0001 | c0001 | t0007 | g0235 | AFR | ACB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG03471 | hp1 | a0001 | c0003 | t0004 | g0045 | AFR | MSL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG03471 | hp2 | a0001 | c0001 | t0011 | g0191 | AFR | MSL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG06807 | hp1 | a0001 | c0001 | t0042 | g0268 | AFR | USA | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | USA | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA18955 | hp2 | a0001 | c0002 | t0002 | g0061 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | USA | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA20300 | hp2 | a0001 | c0001 | t0033 | g0279 | AFR | USA | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA21309 | hp1 | a0001 | c0001 | t0025 | g0002 | AFR | LWK | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
NA21309 | hp2 | a0001 | c0003 | t0004 | g0033 | AFR | LWK | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0007 | g0103 | REF | REF | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0005 | g0251 | REF | REF | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:169713141
|
A | G | 1 | a0002 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.2212A>G | p.Thr738Ala | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/13 | 2714/6635 | 2212/2457 | 738/818 | chr4 | 169713141 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:169636045
|
A | G | 1 | a0001c0008 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.117A>G | p.Gln39Gln | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/13 | 619/6635 | 117/2457 | 39/818 | chr4 | 169636045 | ||
chr4:169689230
|
G | A | 1 | a0001c0004 | 1 | HG03486.hp1 | splice_region_variant&synonymous_variant | LOW | c.606G>A | p.Glu202Glu | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 5/13 | 1108/6635 | 606/2457 | 202/818 | chr4 | 169689230 | ||
chr4:169707085
|
C | T | 1 | a0001c0007 | 1 | HG00733.hp1 | synonymous_variant | LOW | c.1968C>T | p.Asp656Asp | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/13 | 2470/6635 | 1968/2457 | 656/818 | chr4 | 169707085 | ||
chr4:169707241
|
C | T | 1 | a0001c0006 | 1 | NA18974.hp1 | synonymous_variant | LOW | c.2124C>T | p.Leu708Leu | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/13 | 2626/6635 | 2124/2457 | 708/818 | chr4 | 169707241 | ||
chr4:169713239
|
C | T | 2 | a0001c0002a0001c0004 | 67 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(64): Show |
synonymous_variant | LOW | c.2310C>T | p.Ile770Ile | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/13 | 2812/6635 | 2310/2457 | 770/818 | chr4 | 169713239 | ||
chr4:169713257
|
A | G | 1 | a0001c0003 | 50 | HG00639.hp2 HG01175.hp2 HG01346.hp1 others(47): Show |
synonymous_variant | LOW | c.2328A>G | p.Arg776Arg | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/13 | 2830/6635 | 2328/2457 | 776/818 | chr4 | 169713257 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:169620578
|
C | G | 1 | a0001c0001t0025 | 2 | HG02976.hp2 NA21309.hp1 |
5_prime_UTR_variant | MODIFIER | c.-502C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/13 | 15351 | chr4 | 169620578 | |||||
chr4:169620589
|
C | T | 1 | a0001c0001t0024 | 2 | HG03831.hp1 HG04115.hp2 |
5_prime_UTR_variant | MODIFIER | c.-491C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/13 | 15340 | chr4 | 169620589 | |||||
chr4:169620632
|
C | G | 2 | a0001c0001t0052a0001c0002t0051 | 2 | HG02809.hp2 HG02896.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-448C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/13 | chr4 | 169620632 | ||||||
chr4:169635918
|
C | T | 1 | a0001c0002t0050 | 1 | HG01069.hp2 | 5_prime_UTR_variant | MODIFIER | c.-11C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/13 | 11 | chr4 | 169635918 | |||||
chr4:169720232
|
G | A | 1 | a0001c0001t0026 | 1 | NA19074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*235G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 235 | chr4 | 169720232 | |||||
chr4:169720243
|
A | G | 1 | a0001c0003t0049 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*246A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 246 | chr4 | 169720243 | |||||
chr4:169720361
|
A | G | 1 | a0001c0002t0017 | 3 | HG01257.hp1 HG01258.hp2 HG01516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*364A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 364 | chr4 | 169720361 | |||||
chr4:169720526
|
T | TCTCTCTC others(6): Show |
1 | a0001c0001t0027 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*529_*530insCTCTCT others(7): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 530 | chr4 | 169720526 | |||||
chr4:169720526
|
T | TCTCTCTC others(14): Show |
1 | a0001c0001t0028 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*529_*530insCTCTCT others(15): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 530 | chr4 | 169720526 | |||||
chr4:169720526
|
T | TTC | 7 | a0001c0001t0038a0001c0001t0042a0001c0001t0043others(4): Show | 7 | HG01261.hp2 HG02280.hp1 HG02602.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*561_*562dupCT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 563 | INFO_REALIGN_3_PRIME | chr4 | 169720526 | ||||
chr4:169720526
|
T | TTCTCTC | 2 | a0001c0001t0012a0002c0005t0012 | 4 | HG02486.hp2 HG03540.hp1 NA18906.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*557_*562dupCTCTCT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 563 | INFO_REALIGN_3_PRIME | chr4 | 169720526 | ||||
chr4:169720526
|
T | TTCTCTCT others(3): Show |
2 | a0001c0001t0013a0001c0001t0044 | 5 | HG01433.hp2 HG02698.hp2 HG03491.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*553_*562dupCTCTCT others(4): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 563 | INFO_REALIGN_3_PRIME | chr4 | 169720526 | ||||
chr4:169720526
|
T | TTCTCTCT others(5): Show |
2 | a0001c0001t0014a0001c0001t0045 | 5 | HG01099.hp1 HG01243.hp1 HG01517.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*551_*562dupCTCTCT others(6): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 563 | INFO_REALIGN_3_PRIME | chr4 | 169720526 | ||||
chr4:169720526
|
T | TTCTCTCT others(7): Show |
1 | a0001c0001t0010 | 5 | HG00738.hp1 HG01168.hp2 HG01255.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*549_*562dupCTCTCT others(8): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 563 | INFO_REALIGN_3_PRIME | chr4 | 169720526 | ||||
chr4:169720526
|
T | TTCTCTCT others(9): Show |
2 | a0001c0001t0007a0001c0001t0052 | 9 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*547_*562dupCTCTCT others(10): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 563 | INFO_REALIGN_3_PRIME | chr4 | 169720526 | ||||
chr4:169720526
|
T | TTCTCTCT others(11): Show |
1 | a0001c0001t0016 | 3 | HG02040.hp2 HG02602.hp1 HG03688.hp1 |
3_prime_UTR_variant | MODIFIER | c.*545_*562dupCTCTCT others(12): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 563 | INFO_REALIGN_3_PRIME | chr4 | 169720526 | ||||
chr4:169720526
|
T | TTCTCTCT others(13): Show |
2 | a0001c0001t0024a0001c0006t0046 | 3 | HG03831.hp1 HG04115.hp2 NA18974.hp1 |
3_prime_UTR_variant | MODIFIER | c.*543_*562dupCTCTCT others(14): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 563 | INFO_REALIGN_3_PRIME | chr4 | 169720526 | ||||
chr4:169720526
|
T | TTCTCTCT others(19): Show |
1 | a0001c0001t0047 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*537_*562dupCTCTCT others(20): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 563 | INFO_REALIGN_3_PRIME | chr4 | 169720526 | ||||
chr4:169720526
|
T | TTCTCTCT others(21): Show |
1 | a0001c0001t0048 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*535_*562dupCTCTCT others(22): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 563 | INFO_REALIGN_3_PRIME | chr4 | 169720526 | ||||
chr4:169720526
|
TTC | T | 7 | a0001c0001t0015a0001c0001t0021a0001c0002t0008others(4): Show | 34 | HG00639.hp2 HG01175.hp2 HG01496.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*561_*562delCT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 561 | INFO_REALIGN_3_PRIME | chr4 | 169720526 | ||||
chr4:169720526
|
TTCTC | T | 8 | a0001c0001t0001a0001c0001t0018a0001c0001t0019others(5): Show | 94 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*559_*562delCTCT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 559 | INFO_REALIGN_3_PRIME | chr4 | 169720526 | ||||
chr4:169720526
|
TTCTCTCT others(3): Show |
T | 1 | a0001c0001t0011 | 4 | HG02572.hp1 HG02818.hp2 HG03471.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*553_*562delCTCTCT others(4): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 553 | INFO_REALIGN_3_PRIME | chr4 | 169720526 | ||||
chr4:169720526
|
TTCTCTCT others(9): Show |
T | 1 | a0001c0003t0029 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*547_*562delCTCTCT others(10): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 547 | INFO_REALIGN_3_PRIME | chr4 | 169720526 | ||||
chr4:169720923
|
C | G | 2 | a0001c0001t0006a0001c0001t0043 | 9 | HG01884.hp1 HG02572.hp2 HG02602.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*926C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 926 | chr4 | 169720923 | |||||
chr4:169721095
|
A | G | 7 | a0001c0001t0001a0001c0001t0018a0001c0001t0019others(4): Show | 93 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*1098A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 1098 | chr4 | 169721095 | |||||
chr4:169721150
|
A | AT | 2 | a0001c0001t0006a0001c0001t0043 | 9 | HG01884.hp1 HG02572.hp2 HG02602.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1161dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 1162 | INFO_REALIGN_3_PRIME | chr4 | 169721150 | ||||
chr4:169721339
|
T | G | 1 | a0001c0003t0022 | 2 | HG02723.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1342T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 1342 | chr4 | 169721339 | |||||
chr4:169721411
|
T | C | 1 | a0001c0001t0031 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1414T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 1414 | chr4 | 169721411 | |||||
chr4:169721508
|
C | T | 1 | a0001c0001t0042 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1511C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 1511 | chr4 | 169721508 | |||||
chr4:169721509
|
G | A | 2 | a0001c0001t0011a0001c0001t0015 | 7 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1512G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 1512 | chr4 | 169721509 | |||||
chr4:169721530
|
T | TA | 7 | a0001c0001t0025a0001c0003t0004a0001c0003t0020others(4): Show | 25 | HG00639.hp2 HG01175.hp2 HG01358.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1543dupA | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 1544 | INFO_REALIGN_3_PRIME | chr4 | 169721530 | ||||
chr4:169721618
|
C | T | 2 | a0001c0001t0012a0002c0005t0012 | 4 | HG02486.hp2 HG03540.hp1 NA18906.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1621C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 1621 | chr4 | 169721618 | |||||
chr4:169721630
|
C | T | 12 | a0001c0001t0006a0001c0001t0042a0001c0001t0043others(9): Show | 77 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*1633C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 1633 | chr4 | 169721630 | |||||
chr4:169721683
|
G | T | 52 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(49): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
3_prime_UTR_variant | MODIFIER | c.*1686G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 1686 | chr4 | 169721683 | |||||
chr4:169721899
|
G | A | 2 | a0001c0001t0033a0001c0001t0045 | 2 | HG03579.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1902G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 1902 | chr4 | 169721899 | |||||
chr4:169721937
|
C | T | 1 | a0001c0001t0035 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1940C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 1940 | chr4 | 169721937 | |||||
chr4:169722149
|
A | G | 1 | a0001c0002t0036 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2152A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 2152 | chr4 | 169722149 | |||||
chr4:169722564
|
G | T | 1 | a0001c0001t0044 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2567G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 2567 | chr4 | 169722564 | |||||
chr4:169722566
|
T | A | 1 | a0001c0001t0052 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2569T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 2569 | chr4 | 169722566 | |||||
chr4:169723039
|
G | A | 1 | a0001c0001t0018 | 2 | HG00323.hp1 HG01261.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3042G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 3042 | chr4 | 169723039 | |||||
chr4:169723289
|
A | G | 1 | a0001c0003t0020 | 2 | HG02886.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3292A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 3292 | chr4 | 169723289 | |||||
chr4:169723482
|
AT | A | 9 | a0001c0001t0011a0001c0001t0015a0001c0001t0019others(6): Show | 42 | HG01258.hp1 HG01346.hp1 HG01496.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*3498delT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 3498 | INFO_REALIGN_3_PRIME | chr4 | 169723482 | ||||
chr4:169723495
|
T | C | 1 | a0001c0001t0032 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3498T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 3498 | chr4 | 169723495 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:169621146
|
T | G | 1 | a0001c0003t0003g0001 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-17+83T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169621146 | ||||||
chr4:169621162
|
T | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG02257.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-17+99T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169621162 | ||||||
chr4:169621489
|
A | T | 2 | a0001c0001t0033g0279a0001c0001t0045g0280 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-17+426A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169621489 | ||||||
chr4:169621547
|
A | G | 13 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275others(10): Show | 14 | HG02280.hp1 HG02622.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.-17+484A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169621547 | ||||||
chr4:169621658
|
G | T | 1 | a0001c0001t0042g0268 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-17+595G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169621658 | ||||||
chr4:169621707
|
T | C | 1 | a0001c0001t0001g0011 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-17+644T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169621707 | ||||||
chr4:169621876
|
T | C | 1 | a0001c0001t0025g0002 | 2 | HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-17+813T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169621876 | ||||||
chr4:169621927
|
C | T | 1 | a0001c0001t0006g0267 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-17+864C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169621927 | ||||||
chr4:169622048
|
A | T | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | NA18981.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.-17+985A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169622048 | ||||||
chr4:169622050
|
A | G | 3 | a0001c0001t0012g0262a0001c0001t0012g0264a0002c0005t0012g0263 | 3 | HG03540.hp1 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-17+987A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169622050 | ||||||
chr4:169622076
|
C | G | 1 | a0001c0001t0013g0261 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-17+1013C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169622076 | ||||||
chr4:169622179
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-17+1116G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169622179 | ||||||
chr4:169622335
|
C | T | 1 | a0001c0001t0043g0260 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-17+1272C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169622335 | ||||||
chr4:169622481
|
G | A | 265 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(262): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.-17+1418G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169622481 | ||||||
chr4:169622674
|
G | T | 1 | a0001c0001t0031g0242 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-17+1611G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169622674 | ||||||
chr4:169622685
|
G | A | 1 | a0001c0001t0043g0260 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-17+1622G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169622685 | ||||||
chr4:169622813
|
C | T | 1 | a0001c0001t0034g0241 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-17+1750C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169622813 | ||||||
chr4:169622932
|
C | T | 37 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0007g0212others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.-17+1869C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169622932 | ||||||
chr4:169623083
|
CAG | C | 35 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0007g0212others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.-17+2026_-17+2027d others(4): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 169623083 | |||||
chr4:169623105
|
T | C | 5 | a0001c0003t0003g0001a0001c0003t0003g0269a0001c0003t0003g0271others(2): Show | 6 | HG02896.hp2 HG02897.hp1 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17+2042T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169623105 | ||||||
chr4:169623161
|
C | T | 234 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(231): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.-17+2098C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169623161 | ||||||
chr4:169623295
|
G | A | 1 | a0001c0001t0042g0268 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-17+2232G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169623295 | ||||||
chr4:169623398
|
A | G | 3 | a0001c0002t0008g0204a0001c0002t0008g0205a0001c0002t0008g0206 | 3 | HG02965.hp2 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-17+2335A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169623398 | ||||||
chr4:169623730
|
T | A | 1 | a0001c0003t0003g0013 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-17+2667T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169623730 | ||||||
chr4:169623853
|
T | G | 2 | a0001c0001t0052g0030a0001c0002t0051g0031 | 2 | HG02809.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-17+2790T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169623853 | ||||||
chr4:169623888
|
T | C | 33 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(30): Show | 33 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.-17+2825T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169623888 | ||||||
chr4:169623929
|
T | G | 1 | a0001c0002t0002g0032 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-17+2866T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169623929 | ||||||
chr4:169623944
|
C | T | 1 | a0001c0002t0002g0032 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-17+2881C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169623944 | ||||||
chr4:169624223
|
T | C | 3 | a0001c0001t0010g0209a0001c0001t0016g0211a0001c0001t0047g0210 | 3 | HG02602.hp1 HG02738.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.-17+3160T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169624223 | ||||||
chr4:169624268
|
G | A | 54 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(51): Show | 54 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.-17+3205G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169624268 | ||||||
chr4:169624280
|
C | T | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.-17+3217C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169624280 | ||||||
chr4:169624424
|
G | A | 2 | a0001c0001t0025g0002a0001c0001t0034g0241 | 3 | HG02976.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-17+3361G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169624424 | ||||||
chr4:169624428
|
C | T | 2 | a0001c0001t0033g0279a0001c0001t0045g0280 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-17+3365C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169624428 | ||||||
chr4:169624546
|
G | A | 118 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(115): Show | 120 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.-17+3483G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169624546 | ||||||
chr4:169624621
|
T | C | 1 | a0001c0002t0008g0204 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-17+3558T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169624621 | ||||||
chr4:169624624
|
A | G | 9 | a0001c0001t0006g0197a0001c0001t0006g0198a0001c0001t0006g0199others(6): Show | 9 | HG01884.hp1 HG02572.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.-17+3561A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169624624 | ||||||
chr4:169624663
|
G | A | 1 | a0001c0001t0001g0110 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-17+3600G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169624663 | ||||||
chr4:169624936
|
T | C | 6 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(3): Show | 6 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17+3873T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169624936 | ||||||
chr4:169624947
|
A | G | 2 | a0001c0001t0052g0030a0001c0002t0051g0031 | 2 | HG02809.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-17+3884A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169624947 | ||||||
chr4:169625280
|
C | T | 158 | a0001c0001t0006g0197a0001c0001t0006g0198a0001c0001t0006g0199others(155): Show | 162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.-17+4217C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169625280 | ||||||
chr4:169625358
|
A | G | 158 | a0001c0001t0006g0197a0001c0001t0006g0198a0001c0001t0006g0199others(155): Show | 162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.-17+4295A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169625358 | ||||||
chr4:169625358
|
A | T | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-17+4295A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169625358 | ||||||
chr4:169625470
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-17+4407T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169625470 | ||||||
chr4:169625524
|
AG | A | 4 | a0001c0001t0012g0262a0001c0001t0012g0264a0001c0001t0042g0268others(1): Show | 4 | HG03540.hp1 HG06807.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17+4463delG | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 169625524 | |||||
chr4:169625661
|
G | A | 1 | a0001c0001t0033g0279 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-17+4598G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169625661 | ||||||
chr4:169626144
|
G | A | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.-17+5081G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169626144 | ||||||
chr4:169626154
|
A | C | 1 | a0001c0002t0017g0005 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-17+5091A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169626154 | ||||||
chr4:169626195
|
G | A | 3 | a0001c0001t0005g0244a0001c0001t0030g0245a0001c0008t0005g0243 | 3 | HG02055.hp1 HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-17+5132G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169626195 | ||||||
chr4:169626312
|
A | G | 1 | a0001c0001t0001g0187 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-17+5249A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169626312 | ||||||
chr4:169626407
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-17+5344G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169626407 | ||||||
chr4:169626422
|
G | A | 2 | a0001c0001t0025g0002a0001c0001t0034g0241 | 3 | HG02976.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-17+5359G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169626422 | ||||||
chr4:169626435
|
G | A | 1 | a0001c0001t0042g0268 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-17+5372G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169626435 | ||||||
chr4:169626482
|
C | A | 264 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(261): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.-17+5419C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169626482 | ||||||
chr4:169626506
|
C | A | 1 | a0001c0001t0006g0267 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-17+5443C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169626506 | ||||||
chr4:169626514
|
C | A | 3 | a0001c0001t0005g0244a0001c0001t0030g0245a0001c0008t0005g0243 | 3 | HG02055.hp1 HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-17+5451C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169626514 | ||||||
chr4:169626569
|
C | G | 1 | a0001c0001t0006g0267 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-17+5506C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169626569 | ||||||
chr4:169626656
|
G | A | 2 | a0001c0001t0025g0002a0001c0001t0034g0241 | 3 | HG02976.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-17+5593G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169626656 | ||||||
chr4:169626674
|
A | C | 2 | a0001c0001t0052g0030a0001c0002t0051g0031 | 2 | HG02809.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-17+5611A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169626674 | ||||||
chr4:169627296
|
C | T | 1 | a0001c0001t0001g0186 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-17+6233C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169627296 | ||||||
chr4:169627374
|
G | T | 266 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(263): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.-17+6311G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169627374 | ||||||
chr4:169627386
|
T | G | 1 | a0001c0001t0025g0002 | 2 | HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-17+6323T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169627386 | ||||||
chr4:169628177
|
A | G | 8 | a0001c0003t0004g0044a0001c0003t0004g0045a0001c0003t0004g0046others(5): Show | 8 | HG00639.hp2 HG01884.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-17+7114A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169628177 | ||||||
chr4:169628292
|
G | A | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.-17+7229G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169628292 | ||||||
chr4:169628661
|
C | T | 19 | a0001c0003t0004g0033a0001c0003t0004g0034a0001c0003t0004g0036others(16): Show | 19 | HG00639.hp2 HG01175.hp2 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.-16-7252C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169628661 | ||||||
chr4:169628709
|
A | G | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.-16-7204A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169628709 | ||||||
chr4:169628784
|
A | G | 118 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(115): Show | 120 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.-16-7129A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169628784 | ||||||
chr4:169628968
|
G | C | 1 | a0001c0003t0039g0015 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-16-6945G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169628968 | ||||||
chr4:169629017
|
G | A | 2 | a0001c0001t0033g0279a0001c0001t0045g0280 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-16-6896G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169629017 | ||||||
chr4:169629043
|
A | G | 10 | a0001c0003t0004g0034a0001c0003t0004g0036a0001c0003t0004g0037others(7): Show | 10 | HG01175.hp2 HG01358.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-16-6870A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169629043 | ||||||
chr4:169629142
|
G | A | 1 | a0001c0002t0002g0052 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-16-6771G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169629142 | ||||||
chr4:169629176
|
TCTGTATC others(4): Show |
T | 101 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(98): Show | 102 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.-16-6729_-16-6719d others(13): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 169629176 | |||||
chr4:169629223
|
A | G | 3 | a0001c0001t0012g0262a0001c0001t0012g0264a0002c0005t0012g0263 | 3 | HG03540.hp1 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-16-6690A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169629223 | ||||||
chr4:169629278
|
A | AT | 118 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(115): Show | 120 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.-16-6628dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 169629278 | |||||
chr4:169629529
|
C | G | 1 | a0001c0001t0032g0185 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-16-6384C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169629529 | ||||||
chr4:169629663
|
G | A | 1 | a0001c0001t0001g0186 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-16-6250G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169629663 | ||||||
chr4:169629674
|
T | C | 35 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.-16-6239T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169629674 | ||||||
chr4:169629713
|
G | T | 1 | a0001c0002t0002g0109 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-16-6200G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169629713 | ||||||
chr4:169629825
|
A | G | 1 | a0001c0003t0004g0033 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-16-6088A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169629825 | ||||||
chr4:169629874
|
G | A | 3 | a0001c0003t0003g0016a0001c0003t0003g0017a0001c0003t0003g0018 | 3 | HG02886.hp1 HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-16-6039G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169629874 | ||||||
chr4:169630100
|
TTGTAA | T | 40 | a0001c0001t0011g0191a0001c0001t0011g0192a0001c0001t0011g0193others(37): Show | 43 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(40): Show |
intron_variant | MODIFIER | c.-16-5812_-16-5808d others(7): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169630100 | ||||||
chr4:169630174
|
T | G | 1 | a0001c0001t0007g0212 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-16-5739T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169630174 | ||||||
chr4:169630209
|
T | G | 64 | a0001c0001t0007g0103a0001c0002t0002g0004a0001c0002t0002g0032others(61): Show | 66 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.-16-5704T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169630209 | ||||||
chr4:169630222
|
T | C | 94 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(91): Show | 95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.-16-5691T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169630222 | ||||||
chr4:169630227
|
A | G | 3 | a0001c0001t0005g0256a0001c0001t0005g0257a0001c0001t0005g0258 | 3 | HG02622.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-16-5686A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169630227 | ||||||
chr4:169630289
|
G | T | 265 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(262): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.-16-5624G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169630289 | ||||||
chr4:169630294
|
C | T | 1 | a0001c0003t0004g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-16-5619C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169630294 | ||||||
chr4:169630332
|
A | G | 271 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(268): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-16-5581A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169630332 | ||||||
chr4:169630346
|
G | C | 16 | a0001c0001t0011g0191a0001c0001t0011g0192a0001c0001t0011g0193others(13): Show | 17 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(14): Show |
intron_variant | MODIFIER | c.-16-5567G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169630346 | ||||||
chr4:169630421
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-16-5492A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169630421 | ||||||
chr4:169630473
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-16-5440T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169630473 | ||||||
chr4:169630560
|
T | G | 2 | a0001c0001t0033g0279a0001c0001t0045g0280 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-16-5353T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169630560 | ||||||
chr4:169630676
|
AC | A | 2 | a0001c0001t0025g0002a0001c0001t0034g0241 | 3 | HG02976.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-16-5235delC | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 169630676 | |||||
chr4:169630772
|
G | A | 1 | a0001c0001t0012g0259 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-16-5141G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169630772 | ||||||
chr4:169630784
|
C | T | 1 | a0001c0001t0012g0259 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-16-5129C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169630784 | ||||||
chr4:169630819
|
G | A | 13 | a0001c0003t0003g0003a0001c0003t0003g0013a0001c0003t0003g0019others(10): Show | 14 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.-16-5094G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169630819 | ||||||
chr4:169630855
|
A | G | 1 | a0001c0002t0002g0108 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-16-5058A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169630855 | ||||||
chr4:169631008
|
G | GT | 2 | a0001c0001t0025g0002a0001c0001t0034g0241 | 3 | HG02976.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-16-4901dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 169631008 | |||||
chr4:169631186
|
T | C | 1 | a0001c0003t0003g0019 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-16-4727T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169631186 | ||||||
chr4:169631286
|
TTTTG | T | 7 | a0001c0001t0011g0191a0001c0001t0011g0192a0001c0001t0011g0193others(4): Show | 7 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-16-4616_-16-4613d others(6): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 169631286 | |||||
chr4:169631410
|
C | T | 2 | a0001c0001t0033g0279a0001c0001t0045g0280 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-16-4503C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169631410 | ||||||
chr4:169631481
|
G | T | 96 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(93): Show | 97 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.-16-4432G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169631481 | ||||||
chr4:169631489
|
C | T | 1 | a0001c0001t0034g0241 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-16-4424C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169631489 | ||||||
chr4:169631735
|
A | G | 264 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(261): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.-16-4178A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169631735 | ||||||
chr4:169631834
|
G | A | 264 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(261): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.-16-4079G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169631834 | ||||||
chr4:169631850
|
G | A | 264 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(261): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.-16-4063G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169631850 | ||||||
chr4:169631858
|
A | G | 2 | a0001c0001t0033g0279a0001c0001t0045g0280 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-16-4055A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169631858 | ||||||
chr4:169631933
|
C | T | 1 | a0001c0001t0005g0253 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-16-3980C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169631933 | ||||||
chr4:169631960
|
A | C | 1 | a0001c0003t0003g0001 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-16-3953A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169631960 | ||||||
chr4:169632199
|
GATCCA | G | 96 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(93): Show | 97 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.-16-3713_-16-3709d others(7): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169632199 | ||||||
chr4:169632362
|
C | T | 1 | a0001c0002t0002g0107 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-16-3551C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169632362 | ||||||
chr4:169632408
|
C | T | 33 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(30): Show | 33 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.-16-3505C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169632408 | ||||||
chr4:169632409
|
C | T | 3 | a0001c0001t0001g0181a0001c0001t0001g0265a0001c0001t0001g0266 | 3 | NA18981.hp2 NA18986.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-16-3504C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169632409 | ||||||
chr4:169632686
|
C | A | 1 | a0001c0002t0009g0053 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-16-3227C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169632686 | ||||||
chr4:169632716
|
C | CA | 99 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(96): Show | 99 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.-16-3171dupA | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 169632716 | |||||
chr4:169632716
|
C | CAA | 15 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(12): Show | 16 | HG00544.hp2 HG01069.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.-16-3172_-16-3171d others(4): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 169632716 | |||||
chr4:169632716
|
CA | C | 21 | a0001c0001t0011g0191a0001c0001t0011g0192a0001c0001t0015g0190others(18): Show | 21 | HG00639.hp2 HG01175.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.-16-3171delA | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 169632716 | |||||
chr4:169632716
|
CAA | C | 7 | a0001c0001t0011g0193a0001c0001t0011g0194a0001c0001t0015g0195others(4): Show | 7 | HG02451.hp1 HG02615.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-16-3172_-16-3171d others(4): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 169632716 | |||||
chr4:169632716
|
CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0052g0030a0001c0002t0051g0031 | 2 | HG02809.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-16-3181_-16-3171d others(13): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 169632716 | |||||
chr4:169632716
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0002t0008g0106 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-16-3184_-16-3171d others(16): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 169632716 | |||||
chr4:169632841
|
A | G | 1 | a0001c0001t0001g0178 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-16-3072A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169632841 | ||||||
chr4:169632843
|
C | A | 2 | a0001c0001t0052g0030a0001c0002t0051g0031 | 2 | HG02809.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-16-3070C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169632843 | ||||||
chr4:169632947
|
T | A | 3 | a0001c0001t0033g0279a0001c0001t0045g0280a0001c0003t0003g0277 | 3 | HG03139.hp1 HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-16-2966T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169632947 | ||||||
chr4:169633035
|
CAG | C | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.-16-2875_-16-2874d others(4): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 169633035 | |||||
chr4:169633068
|
A | G | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG00544.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.-16-2845A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169633068 | ||||||
chr4:169633262
|
C | T | 1 | a0001c0002t0050g0104 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-16-2651C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169633262 | ||||||
chr4:169633411
|
A | G | 2 | a0001c0001t0033g0279a0001c0001t0045g0280 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-16-2502A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169633411 | ||||||
chr4:169633488
|
TG | T | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.-16-2424delG | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169633488 | ||||||
chr4:169633613
|
A | G | 1 | a0001c0001t0031g0242 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-16-2300A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169633613 | ||||||
chr4:169633763
|
G | A | 2 | a0001c0001t0052g0030a0001c0002t0051g0031 | 2 | HG02809.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-16-2150G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169633763 | ||||||
chr4:169633888
|
G | A | 1 | a0001c0004t0002g0065 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-16-2025G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169633888 | ||||||
chr4:169633906
|
G | A | 1 | a0001c0001t0001g0121 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-16-2007G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169633906 | ||||||
chr4:169633954
|
GT | G | 262 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(259): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.-16-1947delT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 169633954 | |||||
chr4:169633970
|
T | C | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.-16-1943T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169633970 | ||||||
chr4:169634032
|
G | T | 1 | a0001c0001t0001g0187 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-16-1881G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169634032 | ||||||
chr4:169634113
|
C | T | 2 | a0001c0001t0025g0002a0001c0001t0034g0241 | 3 | HG02976.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-16-1800C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169634113 | ||||||
chr4:169634258
|
T | C | 64 | a0001c0001t0007g0103a0001c0002t0002g0004a0001c0002t0002g0032others(61): Show | 66 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.-16-1655T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169634258 | ||||||
chr4:169634349
|
A | T | 1 | a0001c0001t0001g0177 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-16-1564A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169634349 | ||||||
chr4:169634415
|
T | C | 1 | a0001c0001t0016g0219 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-16-1498T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169634415 | ||||||
chr4:169634591
|
A | G | 1 | a0001c0001t0001g0173 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-16-1322A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169634591 | ||||||
chr4:169634773
|
T | C | 2 | a0001c0001t0025g0002a0001c0001t0034g0241 | 3 | HG02976.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-16-1140T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169634773 | ||||||
chr4:169634893
|
T | C | 1 | a0001c0003t0004g0044 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-16-1020T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169634893 | ||||||
chr4:169634970
|
G | T | 5 | a0001c0001t0001g0171a0001c0001t0001g0188a0001c0001t0001g0189others(2): Show | 5 | HG00323.hp1 HG01069.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16-943G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169634970 | ||||||
chr4:169635037
|
G | A | 6 | a0001c0001t0005g0246a0001c0001t0005g0247a0001c0001t0005g0249others(3): Show | 6 | HG01109.hp1 HG02258.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16-876G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169635037 | ||||||
chr4:169635479
|
T | A | 1 | a0001c0001t0043g0260 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-16-434T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169635479 | ||||||
chr4:169635519
|
C | G | 1 | a0001c0001t0001g0169 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-16-394C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169635519 | ||||||
chr4:169635695
|
G | T | 153 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(150): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.-16-218G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169635695 | ||||||
chr4:169635787
|
A | G | 1 | a0001c0001t0045g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-16-126A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169635787 | ||||||
chr4:169635803
|
C | T | 1 | a0001c0001t0035g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-16-110C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169635803 | ||||||
chr4:169635873
|
A | C | 1 | a0001c0002t0002g0101 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-16-40A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169635873 | ||||||
chr4:169636158
|
T | A | 1 | a0001c0001t0047g0210 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.160+70T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169636158 | ||||||
chr4:169636231
|
G | C | 3 | a0001c0001t0012g0262a0001c0001t0012g0264a0002c0005t0012g0263 | 3 | HG03540.hp1 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.160+143G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169636231 | ||||||
chr4:169636315
|
A | G | 11 | a0001c0003t0004g0033a0001c0003t0004g0034a0001c0003t0004g0036others(8): Show | 11 | HG01175.hp2 HG01358.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.160+227A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169636315 | ||||||
chr4:169636399
|
T | A | 5 | a0001c0001t0001g0171a0001c0001t0001g0188a0001c0001t0001g0189others(2): Show | 5 | HG00323.hp1 HG01069.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+311T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169636399 | ||||||
chr4:169636424
|
T | G | 2 | a0001c0001t0012g0262a0002c0005t0012g0263 | 2 | NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.160+336T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169636424 | ||||||
chr4:169636533
|
A | C | 2 | a0001c0001t0033g0279a0001c0001t0045g0280 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.160+445A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169636533 | ||||||
chr4:169636558
|
G | T | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.160+470G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169636558 | ||||||
chr4:169636630
|
T | C | 1 | a0001c0003t0003g0019 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.160+542T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169636630 | ||||||
chr4:169636734
|
G | GGTT | 82 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0125others(79): Show | 86 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.160+647_160+649dup others(3): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169636734 | |||||
chr4:169636735
|
G | GT | 34 | a0001c0001t0005g0244a0001c0001t0005g0246a0001c0001t0005g0247others(31): Show | 34 | HG00639.hp2 HG01109.hp1 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.160+663dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169636735 | |||||
chr4:169636735
|
G | GTTGT | 96 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(93): Show | 98 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.160+649_160+650ins others(4): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169636735 | |||||
chr4:169636735
|
G | GTTGTT | 16 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0006g0197others(13): Show | 16 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.160+649_160+650ins others(5): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169636735 | |||||
chr4:169636737
|
T | TG | 3 | a0001c0003t0003g0017a0001c0003t0003g0018a0001c0003t0003g0029 | 3 | HG02055.hp2 HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.160+649_160+650ins others(1): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169636737 | ||||||
chr4:169636881
|
C | T | 55 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(52): Show | 55 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.160+793C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169636881 | ||||||
chr4:169636901
|
T | C | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.160+813T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169636901 | ||||||
chr4:169636940
|
C | G | 4 | a0001c0002t0008g0204a0001c0002t0008g0205a0001c0002t0008g0206others(1): Show | 4 | HG02809.hp2 HG02965.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+852C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169636940 | ||||||
chr4:169637287
|
A | AT | 94 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(91): Show | 95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.160+1207dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169637287 | |||||
chr4:169637418
|
C | T | 271 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(268): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.160+1330C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169637418 | ||||||
chr4:169637453
|
G | A | 209 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(206): Show | 215 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.160+1365G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169637453 | ||||||
chr4:169637565
|
G | A | 25 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(22): Show | 27 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(24): Show |
intron_variant | MODIFIER | c.160+1477G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169637565 | ||||||
chr4:169637583
|
A | ACAC | 183 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(180): Show | 187 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.160+1507_160+1509d others(5): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169637583 | |||||
chr4:169637595
|
C | A | 1 | a0001c0003t0040g0278 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.160+1507C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169637595 | ||||||
chr4:169637595
|
C | CCAA | 80 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0007g0103others(77): Show | 82 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.160+1520_160+1522d others(5): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169637595 | |||||
chr4:169637598
|
A | C | 3 | a0001c0001t0001g0163a0001c0003t0020g0183a0001c0003t0020g0184 | 3 | HG02886.hp2 NA18965.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.160+1510A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169637598 | ||||||
chr4:169637633
|
C | G | 1 | a0001c0003t0022g0208 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.160+1545C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169637633 | ||||||
chr4:169637745
|
G | A | 209 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(206): Show | 215 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.160+1657G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169637745 | ||||||
chr4:169637774
|
A | G | 2 | a0001c0001t0033g0279a0001c0001t0045g0280 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.160+1686A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169637774 | ||||||
chr4:169638135
|
G | T | 1 | a0001c0001t0025g0002 | 2 | HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.160+2047G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169638135 | ||||||
chr4:169638265
|
G | T | 1 | a0001c0003t0003g0277 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.160+2177G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169638265 | ||||||
chr4:169638289
|
T | C | 42 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0110others(39): Show | 43 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.160+2201T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169638289 | ||||||
chr4:169638357
|
A | G | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.160+2269A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169638357 | ||||||
chr4:169638405
|
T | C | 3 | a0001c0001t0012g0262a0001c0001t0012g0264a0002c0005t0012g0263 | 3 | HG03540.hp1 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.160+2317T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169638405 | ||||||
chr4:169638488
|
A | AT | 208 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(205): Show | 214 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.160+2408dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169638488 | |||||
chr4:169638506
|
A | G | 1 | a0001c0001t0052g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.160+2418A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169638506 | ||||||
chr4:169638639
|
G | A | 1 | a0001c0003t0004g0034 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.160+2551G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169638639 | ||||||
chr4:169638680
|
C | T | 1 | a0001c0001t0007g0217 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.160+2592C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169638680 | ||||||
chr4:169638791
|
T | C | 3 | a0001c0001t0012g0262a0001c0001t0012g0264a0002c0005t0012g0263 | 3 | HG03540.hp1 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.160+2703T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169638791 | ||||||
chr4:169638817
|
C | G | 1 | a0001c0002t0002g0094 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.160+2729C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169638817 | ||||||
chr4:169638979
|
C | T | 2 | a0001c0001t0025g0002a0001c0001t0034g0241 | 3 | HG02976.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.160+2891C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169638979 | ||||||
chr4:169638981
|
A | G | 1 | a0001c0002t0002g0108 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.160+2893A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169638981 | ||||||
chr4:169638988
|
A | C | 264 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(261): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.160+2900A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169638988 | ||||||
chr4:169639180
|
C | T | 96 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(93): Show | 97 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.160+3092C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169639180 | ||||||
chr4:169639208
|
T | G | 2 | a0001c0001t0001g0174a0001c0001t0001g0175 | 2 | NA18955.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.160+3120T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169639208 | ||||||
chr4:169639511
|
A | T | 1 | a0001c0001t0052g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.160+3423A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169639511 | ||||||
chr4:169639707
|
A | G | 64 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0052others(61): Show | 66 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.160+3619A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169639707 | ||||||
chr4:169639771
|
A | G | 1 | a0001c0002t0002g0062 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.160+3683A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169639771 | ||||||
chr4:169639965
|
A | G | 4 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0125others(1): Show | 4 | HG01496.hp2 NA18956.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+3877A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169639965 | ||||||
chr4:169639992
|
T | C | 1 | a0001c0003t0003g0017 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.160+3904T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169639992 | ||||||
chr4:169640008
|
G | A | 21 | a0001c0001t0006g0197a0001c0001t0006g0198a0001c0001t0006g0199others(18): Show | 22 | HG01884.hp1 HG02572.hp1 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.160+3920G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169640008 | ||||||
chr4:169640531
|
C | T | 17 | a0001c0003t0003g0003a0001c0003t0003g0013a0001c0003t0003g0016others(14): Show | 18 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(15): Show |
intron_variant | MODIFIER | c.160+4443C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169640531 | ||||||
chr4:169640713
|
T | C | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.160+4625T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169640713 | ||||||
chr4:169640942
|
C | G | 2 | a0001c0001t0001g0125a0001c0001t0019g0124 | 2 | HG01496.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.160+4854C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169640942 | ||||||
chr4:169640974
|
C | G | 1 | a0001c0003t0003g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+4886C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169640974 | ||||||
chr4:169641027
|
T | C | 1 | a0001c0001t0052g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.160+4939T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169641027 | ||||||
chr4:169641179
|
C | T | 4 | a0001c0002t0008g0204a0001c0002t0008g0205a0001c0002t0008g0206others(1): Show | 4 | HG02809.hp2 HG02965.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+5091C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169641179 | ||||||
chr4:169641447
|
G | A | 55 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(52): Show | 55 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.160+5359G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169641447 | ||||||
chr4:169641490
|
A | G | 1 | a0001c0001t0035g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.160+5402A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169641490 | ||||||
chr4:169641550
|
A | G | 7 | a0001c0002t0002g0061a0001c0002t0002g0090a0001c0002t0002g0091others(4): Show | 7 | HG00558.hp1 HG00621.hp2 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.160+5462A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169641550 | ||||||
chr4:169641580
|
A | C | 1 | a0001c0001t0006g0267 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.160+5492A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169641580 | ||||||
chr4:169641607
|
C | G | 1 | a0001c0003t0003g0272 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.160+5519C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169641607 | ||||||
chr4:169641633
|
A | T | 161 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(158): Show | 164 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.160+5545A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169641633 | ||||||
chr4:169641975
|
A | G | 96 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(93): Show | 97 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.160+5887A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169641975 | ||||||
chr4:169641984
|
A | T | 1 | a0001c0001t0042g0268 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.160+5896A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169641984 | ||||||
chr4:169642002
|
T | C | 218 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(215): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.160+5914T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169642002 | ||||||
chr4:169642127
|
T | A | 1 | a0001c0001t0001g0128 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.160+6039T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169642127 | ||||||
chr4:169642351
|
C | T | 1 | a0001c0003t0037g0040 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.160+6263C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169642351 | ||||||
chr4:169642397
|
C | T | 1 | a0001c0001t0052g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.160+6309C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169642397 | ||||||
chr4:169642582
|
G | A | 55 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(52): Show | 55 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.160+6494G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169642582 | ||||||
chr4:169642795
|
C | T | 183 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(180): Show | 187 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.160+6707C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169642795 | ||||||
chr4:169642833
|
T | A | 1 | a0001c0001t0012g0259 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.160+6745T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169642833 | ||||||
chr4:169642934
|
T | C | 271 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(268): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.160+6846T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169642934 | ||||||
chr4:169643065
|
G | A | 1 | a0001c0001t0012g0259 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.160+6977G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169643065 | ||||||
chr4:169643165
|
A | G | 4 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0032g0185others(1): Show | 4 | HG00099.hp2 HG00642.hp1 HG00733.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+7077A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169643165 | ||||||
chr4:169643405
|
T | C | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.160+7317T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169643405 | ||||||
chr4:169643522
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.160+7434G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169643522 | ||||||
chr4:169643546
|
A | T | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.160+7458A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169643546 | ||||||
chr4:169643618
|
G | T | 1 | a0001c0001t0012g0259 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.160+7530G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169643618 | ||||||
chr4:169643698
|
T | A | 2 | a0001c0001t0033g0279a0001c0001t0045g0280 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.160+7610T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169643698 | ||||||
chr4:169643960
|
A | G | 4 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275others(1): Show | 4 | HG02622.hp1 HG02630.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+7872A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169643960 | ||||||
chr4:169644003
|
G | T | 183 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(180): Show | 187 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.160+7915G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169644003 | ||||||
chr4:169644017
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.160+7929G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169644017 | ||||||
chr4:169644264
|
T | C | 8 | a0001c0001t0011g0191a0001c0001t0011g0192a0001c0001t0011g0193others(5): Show | 8 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.160+8176T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169644264 | ||||||
chr4:169644269
|
C | CT | 9 | a0001c0002t0002g0060a0001c0002t0002g0089a0001c0003t0003g0001others(6): Show | 10 | HG02280.hp1 HG02896.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.160+8195dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169644269 | |||||
chr4:169644314
|
G | A | 1 | a0001c0002t0002g0102 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.160+8226G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169644314 | ||||||
chr4:169644344
|
G | A | 1 | a0001c0001t0024g0218 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.160+8256G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169644344 | ||||||
chr4:169644368
|
G | A | 1 | a0001c0002t0008g0066 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.160+8280G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169644368 | ||||||
chr4:169644420
|
G | A | 1 | a0001c0001t0013g0261 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.160+8332G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169644420 | ||||||
chr4:169644541
|
C | T | 7 | a0001c0003t0003g0001a0001c0003t0003g0269a0001c0003t0003g0271others(4): Show | 8 | HG02280.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.160+8453C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169644541 | ||||||
chr4:169644627
|
C | T | 1 | a0001c0001t0034g0241 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.160+8539C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169644627 | ||||||
chr4:169644699
|
AC | A | 9 | a0001c0001t0006g0197a0001c0001t0006g0198a0001c0001t0006g0199others(6): Show | 9 | HG01884.hp1 HG02572.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.160+8614delC | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169644699 | |||||
chr4:169644869
|
T | C | 1 | a0001c0001t0028g0221 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.160+8781T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169644869 | ||||||
chr4:169644870
|
G | A | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.160+8782G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169644870 | ||||||
chr4:169645002
|
C | A | 2 | a0001c0001t0025g0002a0001c0001t0034g0241 | 3 | HG02976.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.160+8914C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169645002 | ||||||
chr4:169645055
|
TG | T | 2 | a0001c0001t0025g0002a0001c0001t0034g0241 | 3 | HG02976.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.160+8968delG | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169645055 | ||||||
chr4:169645067
|
C | T | 1 | a0001c0001t0025g0002 | 2 | HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.160+8979C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169645067 | ||||||
chr4:169645074
|
T | C | 1 | a0001c0001t0052g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.160+8986T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169645074 | ||||||
chr4:169645157
|
C | A | 36 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(33): Show | 36 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.160+9069C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169645157 | ||||||
chr4:169645284
|
T | TTA | 7 | a0001c0003t0003g0001a0001c0003t0003g0269a0001c0003t0003g0271others(4): Show | 8 | HG02280.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.160+9197_160+9198d others(4): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169645284 | |||||
chr4:169645319
|
C | G | 36 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(33): Show | 36 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.160+9231C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169645319 | ||||||
chr4:169645823
|
G | A | 1 | a0001c0002t0002g0067 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.160+9735G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169645823 | ||||||
chr4:169646132
|
A | G | 2 | a0001c0001t0033g0279a0001c0001t0045g0280 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.160+10044A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169646132 | ||||||
chr4:169646269
|
G | A | 2 | a0001c0003t0020g0183a0001c0003t0020g0184 | 2 | HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.160+10181G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169646269 | ||||||
chr4:169646395
|
T | A | 64 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0052others(61): Show | 66 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.160+10307T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169646395 | ||||||
chr4:169646683
|
T | C | 1 | a0001c0001t0001g0011 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.160+10595T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169646683 | ||||||
chr4:169646862
|
A | C | 1 | a0001c0002t0002g0067 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.160+10774A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169646862 | ||||||
chr4:169647215
|
C | T | 34 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(31): Show | 34 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.160+11127C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169647215 | ||||||
chr4:169647543
|
A | G | 1 | a0001c0001t0052g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.160+11455A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169647543 | ||||||
chr4:169647638
|
A | G | 185 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(182): Show | 189 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.160+11550A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169647638 | ||||||
chr4:169647671
|
T | C | 55 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(52): Show | 55 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.160+11583T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169647671 | ||||||
chr4:169647753
|
T | C | 1 | a0001c0001t0052g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.160+11665T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169647753 | ||||||
chr4:169648021
|
C | T | 185 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(182): Show | 189 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.160+11933C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169648021 | ||||||
chr4:169648122
|
A | G | 2 | a0001c0001t0025g0002a0001c0001t0034g0241 | 3 | HG02976.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.160+12034A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169648122 | ||||||
chr4:169648287
|
G | A | 64 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0052others(61): Show | 66 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.160+12199G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169648287 | ||||||
chr4:169648330
|
A | T | 185 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(182): Show | 189 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.160+12242A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169648330 | ||||||
chr4:169648393
|
G | A | 1 | a0001c0001t0005g0254 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.160+12305G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169648393 | ||||||
chr4:169648428
|
T | C | 55 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(52): Show | 55 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.160+12340T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169648428 | ||||||
chr4:169648567
|
A | C | 1 | a0001c0001t0034g0241 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.160+12479A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169648567 | ||||||
chr4:169648776
|
C | T | 1 | a0001c0001t0006g0267 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.160+12688C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169648776 | ||||||
chr4:169648811
|
A | G | 240 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(237): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.160+12723A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169648811 | ||||||
chr4:169648894
|
G | A | 1 | a0001c0001t0052g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.160+12806G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169648894 | ||||||
chr4:169648942
|
G | A | 12 | a0001c0001t0011g0191a0001c0001t0011g0192a0001c0001t0011g0193others(9): Show | 13 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.160+12854G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169648942 | ||||||
chr4:169648972
|
A | G | 1 | a0001c0002t0002g0094 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.160+12884A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169648972 | ||||||
chr4:169649023
|
T | TA | 12 | a0001c0001t0006g0197a0001c0001t0006g0198a0001c0001t0006g0199others(9): Show | 12 | HG01884.hp1 HG02572.hp2 HG02602.hp2 others(9): Show |
intron_variant | MODIFIER | c.160+12951dupA | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169649023 | |||||
chr4:169649023
|
TA | T | 121 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(118): Show | 124 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.160+12951delA | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169649023 | |||||
chr4:169649087
|
A | C | 1 | a0001c0001t0028g0221 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.160+12999A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169649087 | ||||||
chr4:169649502
|
A | G | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.160+13414A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169649502 | ||||||
chr4:169649577
|
A | T | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.160+13489A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169649577 | ||||||
chr4:169649636
|
T | C | 1 | a0001c0001t0001g0163 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.160+13548T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169649636 | ||||||
chr4:169649702
|
G | T | 8 | a0001c0003t0004g0044a0001c0003t0004g0045a0001c0003t0004g0046others(5): Show | 8 | HG00639.hp2 HG01884.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.160+13614G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169649702 | ||||||
chr4:169649895
|
G | A | 2 | a0001c0001t0007g0214a0001c0001t0007g0217 | 2 | HG00323.hp2 HG00733.hp2 |
intron_variant | MODIFIER | c.160+13807G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169649895 | ||||||
chr4:169649944
|
G | A | 3 | a0001c0001t0001g0171a0001c0001t0018g0170a0001c0001t0018g0172 | 3 | HG00323.hp1 HG01074.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.160+13856G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169649944 | ||||||
chr4:169649957
|
C | T | 1 | a0001c0003t0022g0208 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.160+13869C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169649957 | ||||||
chr4:169650060
|
G | A | 3 | a0001c0001t0012g0262a0001c0001t0012g0264a0002c0005t0012g0263 | 3 | HG03540.hp1 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.160+13972G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169650060 | ||||||
chr4:169650373
|
T | G | 2 | a0001c0001t0033g0279a0001c0001t0045g0280 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.160+14285T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169650373 | ||||||
chr4:169650609
|
T | A | 271 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(268): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.160+14521T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169650609 | ||||||
chr4:169650791
|
A | C | 1 | a0001c0001t0001g0179 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.160+14703A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169650791 | ||||||
chr4:169650844
|
A | G | 2 | a0001c0001t0033g0279a0001c0001t0045g0280 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.160+14756A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169650844 | ||||||
chr4:169651178
|
T | G | 3 | a0001c0001t0001g0113a0001c0001t0001g0130a0001c0001t0001g0131 | 3 | NA19068.hp2 NA19078.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.160+15090T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169651178 | ||||||
chr4:169651221
|
T | G | 2 | a0001c0001t0033g0279a0001c0001t0045g0280 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.160+15133T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169651221 | ||||||
chr4:169651554
|
A | G | 1 | a0001c0002t0008g0066 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.160+15466A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169651554 | ||||||
chr4:169651667
|
G | A | 1 | a0001c0001t0001g0009 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.160+15579G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169651667 | ||||||
chr4:169651833
|
T | A | 1 | a0001c0001t0026g0132 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.160+15745T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169651833 | ||||||
chr4:169652136
|
G | A | 2 | a0001c0003t0020g0183a0001c0003t0020g0184 | 2 | HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.160+16048G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169652136 | ||||||
chr4:169652145
|
A | G | 23 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(20): Show | 25 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(22): Show |
intron_variant | MODIFIER | c.160+16057A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169652145 | ||||||
chr4:169652291
|
A | G | 1 | a0001c0001t0001g0123 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.160+16203A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169652291 | ||||||
chr4:169652446
|
G | A | 1 | a0001c0001t0001g0163 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.160+16358G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169652446 | ||||||
chr4:169652499
|
T | A | 3 | a0001c0001t0001g0171a0001c0001t0018g0170a0001c0001t0018g0172 | 3 | HG00323.hp1 HG01074.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.160+16411T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169652499 | ||||||
chr4:169652572
|
G | A | 1 | a0001c0002t0002g0101 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.160+16484G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169652572 | ||||||
chr4:169652795
|
T | C | 1 | a0001c0002t0017g0005 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.160+16707T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169652795 | ||||||
chr4:169653141
|
C | T | 11 | a0001c0003t0004g0033a0001c0003t0004g0034a0001c0003t0004g0036others(8): Show | 11 | HG01175.hp2 HG01358.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.160+17053C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169653141 | ||||||
chr4:169653148
|
A | G | 7 | a0001c0001t0011g0191a0001c0001t0011g0192a0001c0001t0011g0193others(4): Show | 7 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+17060A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169653148 | ||||||
chr4:169653262
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.160+17174G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169653262 | ||||||
chr4:169653332
|
C | T | 2 | a0001c0001t0033g0279a0001c0001t0045g0280 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.160+17244C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169653332 | ||||||
chr4:169653514
|
G | A | 8 | a0001c0003t0004g0044a0001c0003t0004g0045a0001c0003t0004g0046others(5): Show | 8 | HG00639.hp2 HG01884.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.160+17426G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169653514 | ||||||
chr4:169653553
|
A | G | 1 | a0001c0001t0025g0002 | 2 | HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.160+17465A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169653553 | ||||||
chr4:169653640
|
C | CA | 173 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(170): Show | 177 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.160+17573dupA | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169653640 | |||||
chr4:169653640
|
C | CAA | 46 | a0001c0001t0001g0123a0001c0001t0001g0133a0001c0001t0001g0134others(43): Show | 46 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.160+17572_160+1757 others(6): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169653640 | |||||
chr4:169653640
|
C | CAAA | 19 | a0001c0001t0011g0191a0001c0001t0011g0192a0001c0001t0011g0193others(16): Show | 19 | HG00639.hp2 HG01884.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.160+17571_160+1757 others(7): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169653640 | |||||
chr4:169653677
|
C | T | 2 | a0001c0003t0020g0183a0001c0003t0020g0184 | 2 | HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.160+17589C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169653677 | ||||||
chr4:169653678
|
G | C | 1 | a0001c0001t0001g0179 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.160+17590G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169653678 | ||||||
chr4:169653777
|
G | A | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.160+17689G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169653777 | ||||||
chr4:169653872
|
A | G | 2 | a0001c0001t0033g0279a0001c0001t0045g0280 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.160+17784A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169653872 | ||||||
chr4:169654054
|
A | C | 5 | a0001c0001t0005g0244a0001c0001t0005g0254a0001c0001t0005g0255others(2): Show | 5 | HG02055.hp1 HG02258.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.160+17966A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169654054 | ||||||
chr4:169654092
|
G | C | 62 | a0001c0002t0002g0004a0001c0002t0002g0052a0001c0002t0002g0054others(59): Show | 64 | HG00140.hp2 HG00558.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.160+18004G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169654092 | ||||||
chr4:169654162
|
G | T | 1 | a0001c0001t0001g0128 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.160+18074G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169654162 | ||||||
chr4:169654166
|
G | A | 1 | a0001c0001t0042g0268 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.160+18078G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169654166 | ||||||
chr4:169654234
|
C | G | 2 | a0001c0001t0033g0279a0001c0001t0045g0280 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.160+18146C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169654234 | ||||||
chr4:169654700
|
C | T | 271 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(268): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.160+18612C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169654700 | ||||||
chr4:169654758
|
A | T | 1 | a0001c0003t0003g0277 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.160+18670A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169654758 | ||||||
chr4:169654860
|
A | G | 2 | a0001c0001t0033g0279a0001c0001t0045g0280 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.160+18772A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169654860 | ||||||
chr4:169654918
|
T | G | 47 | a0001c0001t0033g0279a0001c0001t0045g0280a0001c0003t0003g0001others(44): Show | 49 | HG00639.hp2 HG01175.hp2 HG01346.hp1 others(46): Show |
intron_variant | MODIFIER | c.160+18830T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169654918 | ||||||
chr4:169654948
|
A | G | 1 | a0001c0001t0042g0268 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.160+18860A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169654948 | ||||||
chr4:169655059
|
A | T | 1 | a0001c0001t0001g0182 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.160+18971A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169655059 | ||||||
chr4:169655114
|
A | G | 1 | a0001c0001t0042g0268 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.160+19026A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169655114 | ||||||
chr4:169655116
|
A | G | 3 | a0001c0003t0003g0277a0001c0003t0022g0207a0001c0003t0022g0208 | 3 | HG02723.hp2 HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.160+19028A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169655116 | ||||||
chr4:169655192
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.160+19104T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169655192 | ||||||
chr4:169655279
|
C | T | 1 | a0001c0002t0050g0104 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.160+19191C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169655279 | ||||||
chr4:169655623
|
T | C | 26 | a0001c0001t0033g0279a0001c0001t0045g0280a0001c0003t0003g0001others(23): Show | 28 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(25): Show |
intron_variant | MODIFIER | c.160+19535T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169655623 | ||||||
chr4:169655873
|
C | T | 1 | a0001c0001t0012g0259 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.160+19785C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169655873 | ||||||
chr4:169656097
|
C | T | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.160+20009C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169656097 | ||||||
chr4:169656103
|
A | G | 5 | a0001c0002t0009g0053a0001c0002t0009g0096a0001c0002t0009g0097others(2): Show | 5 | HG02109.hp2 HG02451.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+20015A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169656103 | ||||||
chr4:169656268
|
G | A | 1 | a0001c0008t0005g0243 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.160+20180G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169656268 | ||||||
chr4:169656269
|
C | T | 2 | a0001c0003t0003g0003a0001c0003t0003g0028 | 3 | HG01516.hp2 HG01517.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.160+20181C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169656269 | ||||||
chr4:169656279
|
C | A | 1 | a0001c0001t0006g0197 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.160+20191C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169656279 | ||||||
chr4:169656439
|
A | T | 2 | a0001c0001t0025g0002a0001c0001t0034g0241 | 3 | HG02976.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.160+20351A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169656439 | ||||||
chr4:169656488
|
A | G | 9 | a0001c0001t0006g0197a0001c0001t0006g0198a0001c0001t0006g0199others(6): Show | 9 | HG01884.hp1 HG02572.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.160+20400A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169656488 | ||||||
chr4:169656501
|
C | A | 1 | a0001c0001t0001g0114 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.160+20413C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169656501 | ||||||
chr4:169656551
|
G | A | 1 | a0001c0003t0023g0035 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.160+20463G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169656551 | ||||||
chr4:169656751
|
C | T | 31 | a0001c0001t0005g0244a0001c0001t0005g0254a0001c0001t0005g0255others(28): Show | 33 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(30): Show |
intron_variant | MODIFIER | c.160+20663C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169656751 | ||||||
chr4:169656828
|
G | A | 1 | a0001c0001t0012g0259 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.160+20740G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169656828 | ||||||
chr4:169656953
|
T | C | 1 | a0001c0001t0034g0241 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.160+20865T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169656953 | ||||||
chr4:169657058
|
A | G | 2 | a0001c0001t0010g0236a0001c0001t0010g0238 | 2 | HG00738.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.160+20970A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169657058 | ||||||
chr4:169657212
|
A | G | 1 | a0001c0002t0008g0086 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.160+21124A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169657212 | ||||||
chr4:169657270
|
A | G | 54 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0052others(51): Show | 56 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.160+21182A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169657270 | ||||||
chr4:169657389
|
T | C | 47 | a0001c0001t0033g0279a0001c0001t0045g0280a0001c0003t0003g0001others(44): Show | 49 | HG00639.hp2 HG01175.hp2 HG01346.hp1 others(46): Show |
intron_variant | MODIFIER | c.160+21301T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169657389 | ||||||
chr4:169657471
|
C | CA | 64 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0052others(61): Show | 66 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.160+21389dupA | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169657471 | |||||
chr4:169657642
|
G | C | 1 | a0001c0002t0002g0068 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.160+21554G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169657642 | ||||||
chr4:169657644
|
T | C | 1 | a0001c0002t0008g0066 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.160+21556T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169657644 | ||||||
chr4:169657774
|
T | G | 1 | a0001c0001t0034g0241 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.160+21686T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169657774 | ||||||
chr4:169657851
|
C | A | 101 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(98): Show | 103 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.160+21763C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169657851 | ||||||
chr4:169658017
|
G | C | 1 | a0001c0003t0003g0003 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.160+21929G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169658017 | ||||||
chr4:169658183
|
A | G | 1 | a0001c0003t0004g0039 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.161-21867A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169658183 | ||||||
chr4:169658187
|
G | T | 1 | a0001c0001t0005g0250 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.161-21863G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169658187 | ||||||
chr4:169658224
|
ATATAAT | A | 2 | a0001c0001t0025g0002a0001c0001t0034g0241 | 3 | HG02976.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.161-21821_161-2181 others(10): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169658224 | |||||
chr4:169658232
|
A | T | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.161-21818A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169658232 | ||||||
chr4:169658239
|
TATATA | T | 65 | a0001c0001t0042g0268a0001c0002t0002g0004a0001c0002t0002g0032others(62): Show | 67 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.161-21810_161-2180 others(9): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169658239 | ||||||
chr4:169658248
|
T | C | 35 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.161-21802T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169658248 | ||||||
chr4:169658308
|
A | G | 3 | a0001c0001t0033g0279a0001c0001t0034g0241a0001c0001t0045g0280 | 3 | HG03579.hp2 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.161-21742A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169658308 | ||||||
chr4:169658434
|
A | G | 65 | a0001c0001t0042g0268a0001c0002t0002g0004a0001c0002t0002g0032others(62): Show | 67 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.161-21616A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169658434 | ||||||
chr4:169659053
|
G | A | 2 | a0001c0002t0002g0069a0001c0002t0002g0089 | 2 | NA18956.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.161-20997G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169659053 | ||||||
chr4:169659094
|
A | C | 2 | a0001c0001t0006g0201a0001c0001t0006g0202 | 2 | HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.161-20956A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169659094 | ||||||
chr4:169659160
|
TG | T | 5 | a0001c0001t0005g0244a0001c0001t0005g0254a0001c0001t0005g0255others(2): Show | 5 | HG02055.hp1 HG02258.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-20889delG | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169659160 | ||||||
chr4:169659176
|
T | C | 2 | a0001c0001t0025g0002a0001c0001t0034g0241 | 3 | HG02976.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.161-20874T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169659176 | ||||||
chr4:169659276
|
G | A | 1 | a0001c0003t0003g0269 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.161-20774G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169659276 | ||||||
chr4:169659377
|
A | T | 2 | a0001c0003t0020g0183a0001c0003t0020g0184 | 2 | HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.161-20673A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169659377 | ||||||
chr4:169659486
|
C | T | 147 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(144): Show | 151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.161-20564C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169659486 | ||||||
chr4:169659626
|
C | T | 26 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(23): Show | 28 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(25): Show |
intron_variant | MODIFIER | c.161-20424C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169659626 | ||||||
chr4:169659665
|
ACT | A | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.161-20382_161-2038 others(6): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169659665 | |||||
chr4:169659667
|
T | C | 88 | a0001c0001t0033g0279a0001c0001t0042g0268a0001c0001t0045g0280others(85): Show | 90 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.161-20383T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169659667 | ||||||
chr4:169659721
|
A | AT | 18 | a0001c0001t0025g0002a0001c0003t0003g0003a0001c0003t0003g0013others(15): Show | 20 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(17): Show |
intron_variant | MODIFIER | c.161-20319dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169659721 | |||||
chr4:169659791
|
T | A | 1 | a0001c0003t0003g0029 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.161-20259T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169659791 | ||||||
chr4:169660075
|
G | A | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.161-19975G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169660075 | ||||||
chr4:169660419
|
G | A | 266 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(263): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.161-19631G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169660419 | ||||||
chr4:169660441
|
T | C | 6 | a0001c0001t0005g0246a0001c0001t0005g0247a0001c0001t0005g0249others(3): Show | 6 | HG01109.hp1 HG02258.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-19609T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169660441 | ||||||
chr4:169660476
|
T | G | 1 | a0001c0001t0005g0244 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.161-19574T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169660476 | ||||||
chr4:169660497
|
C | T | 1 | a0001c0001t0001g0160 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.161-19553C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169660497 | ||||||
chr4:169660573
|
G | T | 2 | a0001c0001t0033g0279a0001c0001t0045g0280 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.161-19477G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169660573 | ||||||
chr4:169661078
|
AAAT | A | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.161-18967_161-1896 others(7): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169661078 | |||||
chr4:169661095
|
G | A | 1 | a0001c0007t0001g0162 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.161-18955G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169661095 | ||||||
chr4:169661213
|
T | C | 1 | a0001c0001t0042g0268 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.161-18837T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169661213 | ||||||
chr4:169661317
|
A | G | 5 | a0001c0002t0002g0059a0001c0002t0002g0082a0001c0002t0002g0083others(2): Show | 5 | HG01192.hp2 HG01243.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-18733A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169661317 | ||||||
chr4:169661398
|
T | G | 3 | a0001c0003t0003g0013a0001c0003t0003g0023a0001c0003t0003g0024 | 3 | NA18982.hp1 NA18984.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.161-18652T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169661398 | ||||||
chr4:169661493
|
A | G | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.161-18557A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169661493 | ||||||
chr4:169661699
|
T | C | 1 | a0001c0002t0002g0070 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.161-18351T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169661699 | ||||||
chr4:169661774
|
C | T | 1 | a0001c0003t0004g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.161-18276C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169661774 | ||||||
chr4:169661837
|
A | G | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.161-18213A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169661837 | ||||||
chr4:169661838
|
T | C | 1 | a0001c0003t0003g0277 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.161-18212T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169661838 | ||||||
chr4:169662006
|
G | A | 59 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(56): Show | 61 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.161-18044G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169662006 | ||||||
chr4:169662208
|
T | C | 4 | a0001c0001t0001g0012a0001c0001t0001g0115a0001c0001t0001g0135others(1): Show | 4 | HG00544.hp2 HG01071.hp2 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-17842T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169662208 | ||||||
chr4:169662231
|
A | G | 1 | a0001c0001t0052g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.161-17819A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169662231 | ||||||
chr4:169662435
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.161-17615A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169662435 | ||||||
chr4:169662514
|
A | T | 54 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0052others(51): Show | 56 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.161-17536A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169662514 | ||||||
chr4:169662711
|
C | T | 3 | a0001c0001t0012g0262a0001c0001t0012g0264a0002c0005t0012g0263 | 3 | HG03540.hp1 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.161-17339C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169662711 | ||||||
chr4:169662854
|
G | A | 1 | a0001c0003t0003g0277 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.161-17196G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169662854 | ||||||
chr4:169663125
|
ATG | A | 198 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(195): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.161-16901_161-1690 others(6): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169663125 | |||||
chr4:169663125
|
ATGTG | A | 2 | a0001c0001t0005g0244a0001c0001t0025g0002 | 3 | HG02976.hp2 HG03540.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.161-16903_161-1690 others(8): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169663125 | |||||
chr4:169663129
|
GTGTGTGT others(21): Show |
G | 2 | a0001c0001t0033g0279a0001c0001t0045g0280 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.161-16908_161-1688 others(32): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169663129 | |||||
chr4:169663131
|
GTGTGTGT others(19): Show |
G | 45 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(42): Show | 47 | HG00639.hp2 HG01175.hp2 HG01346.hp1 others(44): Show |
intron_variant | MODIFIER | c.161-16906_161-1688 others(30): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169663131 | |||||
chr4:169663133
|
GTGTGTGT others(17): Show |
G | 2 | a0001c0003t0003g0022a0001c0003t0004g0034 | 2 | HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.161-16904_161-1688 others(28): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169663133 | |||||
chr4:169663149
|
G | A | 9 | a0001c0001t0006g0197a0001c0001t0006g0198a0001c0001t0006g0199others(6): Show | 9 | HG01884.hp1 HG02572.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.161-16901G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663149 | ||||||
chr4:169663149
|
GTA | G | 5 | a0001c0001t0001g0148a0001c0001t0001g0174a0001c0001t0001g0175others(2): Show | 6 | HG01257.hp1 HG01258.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-16893_161-1689 others(6): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169663149 | |||||
chr4:169663171
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.161-16879G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663171 | ||||||
chr4:169663179
|
G | GTA | 38 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(35): Show | 38 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.161-16858_161-1685 others(6): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169663179 | |||||
chr4:169663192
|
T | A | 5 | a0001c0003t0004g0037a0001c0003t0004g0039a0001c0003t0004g0041others(2): Show | 5 | HG01175.hp2 HG02451.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-16858T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663192 | ||||||
chr4:169663194
|
C | T | 2 | a0001c0003t0020g0183a0001c0003t0020g0184 | 2 | HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.161-16856C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663194 | ||||||
chr4:169663196
|
T | C | 2 | a0001c0003t0020g0183a0001c0003t0020g0184 | 2 | HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.161-16854T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663196 | ||||||
chr4:169663198
|
TAC | T | 21 | a0001c0003t0004g0033a0001c0003t0004g0034a0001c0003t0004g0036others(18): Show | 21 | HG00639.hp2 HG01175.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.161-16844_161-1684 others(6): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169663198 | |||||
chr4:169663200
|
C | T | 2 | a0001c0003t0020g0183a0001c0003t0020g0184 | 2 | HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.161-16850C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663200 | ||||||
chr4:169663214
|
A | G | 2 | a0001c0001t0033g0279a0001c0001t0045g0280 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.161-16836A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663214 | ||||||
chr4:169663310
|
T | G | 23 | a0001c0003t0004g0033a0001c0003t0004g0034a0001c0003t0004g0036others(20): Show | 23 | HG00639.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.161-16740T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663310 | ||||||
chr4:169663311
|
TTTTTTG | T | 3 | a0001c0001t0024g0218a0001c0001t0033g0279a0001c0001t0045g0280 | 3 | HG03579.hp2 HG03831.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.161-16736_161-1673 others(10): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169663311 | |||||
chr4:169663314
|
T | G | 1 | a0001c0001t0006g0201 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.161-16736T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663314 | ||||||
chr4:169663314
|
TTTGTTG | T | 196 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(193): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.161-16709_161-1670 others(10): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169663314 | |||||
chr4:169663315
|
TTGTTG | T | 22 | a0001c0002t0008g0204a0001c0003t0004g0033a0001c0003t0004g0034others(19): Show | 22 | HG00639.hp2 HG01175.hp2 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.161-16733_161-1672 others(9): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169663315 | |||||
chr4:169663316
|
TGTTGTTG | T | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.161-16733_161-1672 others(11): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663316 | ||||||
chr4:169663317
|
G | T | 4 | a0001c0001t0005g0249a0001c0001t0006g0197a0001c0001t0006g0200others(1): Show | 4 | HG01884.hp1 HG02258.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.161-16733G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663317 | ||||||
chr4:169663323
|
G | T | 79 | a0001c0001t0001g0161a0001c0001t0012g0262a0001c0001t0012g0264others(76): Show | 81 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.161-16727G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663323 | ||||||
chr4:169663326
|
G | T | 11 | a0001c0002t0008g0204a0001c0002t0008g0205a0001c0002t0008g0206others(8): Show | 12 | HG02280.hp1 HG02809.hp2 HG02896.hp2 others(9): Show |
intron_variant | MODIFIER | c.161-16724G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663326 | ||||||
chr4:169663408
|
A | C | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.161-16642A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663408 | ||||||
chr4:169663441
|
C | T | 1 | a0001c0001t0006g0202 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.161-16609C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663441 | ||||||
chr4:169663452
|
C | T | 1 | a0001c0001t0014g0234 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.161-16598C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663452 | ||||||
chr4:169663474
|
C | T | 3 | a0001c0002t0002g0055a0001c0002t0002g0063a0001c0002t0002g0064 | 3 | HG01978.hp1 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.161-16576C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663474 | ||||||
chr4:169663510
|
A | AT | 24 | a0001c0001t0007g0212a0001c0003t0003g0001a0001c0003t0003g0003others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.161-16526dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169663510 | |||||
chr4:169663552
|
C | G | 35 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.161-16498C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663552 | ||||||
chr4:169663622
|
G | A | 2 | a0001c0001t0001g0273a0001c0001t0001g0276 | 2 | HG02622.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.161-16428G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663622 | ||||||
chr4:169663637
|
G | C | 1 | a0001c0001t0045g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.161-16413G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663637 | ||||||
chr4:169663729
|
G | A | 64 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0052others(61): Show | 66 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.161-16321G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663729 | ||||||
chr4:169663992
|
G | A | 4 | a0001c0001t0001g0012a0001c0001t0001g0115a0001c0001t0001g0135others(1): Show | 4 | HG00544.hp2 HG01071.hp2 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-16058G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663992 | ||||||
chr4:169664022
|
A | G | 35 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.161-16028A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169664022 | ||||||
chr4:169664064
|
G | T | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.161-15986G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169664064 | ||||||
chr4:169664215
|
T | A | 1 | a0001c0001t0001g0137 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.161-15835T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169664215 | ||||||
chr4:169664301
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.161-15749C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169664301 | ||||||
chr4:169664349
|
A | G | 1 | a0001c0001t0042g0268 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.161-15701A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169664349 | ||||||
chr4:169664355
|
A | G | 34 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(31): Show | 34 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.161-15695A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169664355 | ||||||
chr4:169664408
|
A | G | 23 | a0001c0003t0004g0033a0001c0003t0004g0034a0001c0003t0004g0036others(20): Show | 23 | HG00639.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.161-15642A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169664408 | ||||||
chr4:169664435
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.161-15615T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169664435 | ||||||
chr4:169664888
|
G | A | 1 | a0001c0001t0001g0110 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.161-15162G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169664888 | ||||||
chr4:169665356
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.161-14694A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169665356 | ||||||
chr4:169665603
|
GA | G | 152 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(149): Show | 156 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.161-14436delA | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169665603 | |||||
chr4:169665642
|
A | G | 35 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.161-14408A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169665642 | ||||||
chr4:169665868
|
G | A | 1 | a0001c0001t0042g0268 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.161-14182G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169665868 | ||||||
chr4:169665960
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.161-14090G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169665960 | ||||||
chr4:169665980
|
G | GT | 35 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.161-14057dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169665980 | |||||
chr4:169665980
|
G | T | 63 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0052others(60): Show | 65 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.161-14070G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169665980 | ||||||
chr4:169666097
|
G | A | 34 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(31): Show | 34 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.161-13953G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169666097 | ||||||
chr4:169666206
|
C | G | 1 | a0001c0001t0042g0268 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.161-13844C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169666206 | ||||||
chr4:169666257
|
A | G | 2 | a0001c0003t0003g0269a0001c0003t0003g0271 | 2 | HG03704.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.161-13793A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169666257 | ||||||
chr4:169666267
|
A | G | 23 | a0001c0003t0004g0033a0001c0003t0004g0034a0001c0003t0004g0036others(20): Show | 23 | HG00639.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.161-13783A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169666267 | ||||||
chr4:169666503
|
A | G | 6 | a0001c0001t0005g0246a0001c0001t0005g0247a0001c0001t0005g0249others(3): Show | 6 | HG01109.hp1 HG02258.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-13547A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169666503 | ||||||
chr4:169666994
|
G | T | 35 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.161-13056G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169666994 | ||||||
chr4:169667144
|
G | T | 1 | a0001c0001t0028g0221 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.161-12906G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169667144 | ||||||
chr4:169667296
|
CT | C | 27 | a0001c0001t0012g0262a0001c0001t0012g0264a0001c0003t0003g0001others(24): Show | 29 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(26): Show |
intron_variant | MODIFIER | c.161-12744delT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169667296 | |||||
chr4:169667316
|
C | T | 1 | a0001c0002t0009g0099 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.161-12734C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169667316 | ||||||
chr4:169667433
|
A | G | 1 | a0001c0001t0035g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.161-12617A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169667433 | ||||||
chr4:169667465
|
T | C | 1 | a0001c0001t0048g0225 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.161-12585T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169667465 | ||||||
chr4:169667521
|
A | G | 1 | a0001c0003t0003g0277 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.161-12529A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169667521 | ||||||
chr4:169667680
|
T | TAAAAATA others(309): Show |
21 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(18): Show | 21 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.161-12352_161-1235 others(320): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169667680 | |||||
chr4:169667680
|
T | TAAAAATA others(310): Show |
5 | a0001c0001t0016g0226a0001c0001t0024g0218a0001c0001t0024g0222others(2): Show | 5 | HG02896.hp1 HG03688.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.161-12352_161-1235 others(321): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169667680 | |||||
chr4:169667680
|
T | TAAAAATA others(309): Show |
8 | a0001c0001t0010g0236a0001c0001t0010g0238a0001c0001t0013g0233others(5): Show | 8 | HG00738.hp1 HG01168.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.161-12352_161-1235 others(320): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169667680 | |||||
chr4:169667680
|
T | TAAAAATA others(310): Show |
1 | a0001c0001t0014g0229 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.161-12352_161-1235 others(321): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169667680 | |||||
chr4:169667690
|
G | A | 1 | a0001c0001t0001g0110 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.161-12360G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169667690 | ||||||
chr4:169667753
|
C | CT | 10 | a0001c0001t0006g0197a0001c0001t0006g0198a0001c0001t0006g0199others(7): Show | 10 | HG00609.hp1 HG01884.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.161-12286dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169667753 | |||||
chr4:169667776
|
C | T | 1 | a0001c0001t0010g0224 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.161-12274C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169667776 | ||||||
chr4:169667907
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.161-12143G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169667907 | ||||||
chr4:169667927
|
G | C | 9 | a0001c0001t0006g0197a0001c0001t0006g0198a0001c0001t0006g0199others(6): Show | 9 | HG01884.hp1 HG02572.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.161-12123G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169667927 | ||||||
chr4:169667985
|
T | C | 149 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(146): Show | 153 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.161-12065T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169667985 | ||||||
chr4:169668043
|
A | AT | 89 | a0001c0001t0001g0112a0001c0001t0001g0123a0001c0001t0001g0125others(86): Show | 91 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.161-11984dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169668043 | |||||
chr4:169668043
|
A | ATT | 25 | a0001c0001t0012g0264a0001c0002t0002g0058a0001c0002t0002g0062others(22): Show | 27 | HG01175.hp2 HG01257.hp1 HG01258.hp2 others(24): Show |
intron_variant | MODIFIER | c.161-11985_161-1198 others(6): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169668043 | |||||
chr4:169668043
|
A | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0143 | 3 | HG01346.hp2 HG01433.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.161-12007A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169668043 | ||||||
chr4:169668043
|
A | T | 2 | a0001c0001t0001g0121a0001c0003t0003g0277 | 2 | HG03139.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.161-12007A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169668043 | ||||||
chr4:169668046
|
T | TG | 31 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(28): Show | 31 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.161-12004_161-1200 others(5): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169668046 | ||||||
chr4:169668047
|
T | G | 1 | a0001c0001t0052g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.161-12003T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169668047 | ||||||
chr4:169668166
|
GGTT | G | 64 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0052others(61): Show | 66 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.161-11880_161-1187 others(7): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169668166 | |||||
chr4:169668214
|
C | T | 1 | a0001c0001t0011g0191 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.161-11836C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169668214 | ||||||
chr4:169668474
|
A | G | 1 | a0001c0001t0042g0268 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.161-11576A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169668474 | ||||||
chr4:169668523
|
C | T | 17 | a0001c0001t0006g0197a0001c0001t0006g0198a0001c0001t0006g0199others(14): Show | 17 | HG01884.hp1 HG02572.hp1 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.161-11527C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169668523 | ||||||
chr4:169668616
|
G | A | 1 | a0001c0001t0035g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.161-11434G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169668616 | ||||||
chr4:169668730
|
A | AT | 7 | a0001c0001t0001g0137a0001c0001t0001g0266a0001c0001t0010g0238others(4): Show | 7 | HG01168.hp2 HG02896.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.161-11305dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169668730 | |||||
chr4:169668730
|
A | ATT | 33 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(30): Show | 33 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.161-11306_161-1130 others(6): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169668730 | |||||
chr4:169668730
|
AT | A | 29 | a0001c0001t0001g0122a0001c0001t0005g0244a0001c0001t0005g0254others(26): Show | 30 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(27): Show |
intron_variant | MODIFIER | c.161-11305delT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169668730 | |||||
chr4:169668928
|
G | A | 1 | a0001c0002t0002g0090 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.161-11122G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169668928 | ||||||
chr4:169669080
|
G | C | 1 | a0001c0003t0004g0050 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.161-10970G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169669080 | ||||||
chr4:169669238
|
A | G | 94 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(91): Show | 95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.161-10812A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169669238 | ||||||
chr4:169669240
|
C | T | 1 | a0001c0003t0003g0003 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.161-10810C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169669240 | ||||||
chr4:169669789
|
G | A | 47 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(44): Show | 49 | HG00639.hp2 HG01175.hp2 HG01346.hp1 others(46): Show |
intron_variant | MODIFIER | c.161-10261G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169669789 | ||||||
chr4:169669832
|
C | T | 7 | a0001c0001t0011g0191a0001c0001t0011g0192a0001c0001t0011g0193others(4): Show | 7 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.161-10218C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169669832 | ||||||
chr4:169669838
|
A | G | 47 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(44): Show | 49 | HG00639.hp2 HG01175.hp2 HG01346.hp1 others(46): Show |
intron_variant | MODIFIER | c.161-10212A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169669838 | ||||||
chr4:169669843
|
A | G | 3 | a0001c0002t0002g0058a0001c0002t0002g0072a0001c0002t0002g0080 | 3 | NA18947.hp2 NA18981.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.161-10207A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169669843 | ||||||
chr4:169670328
|
G | A | 8 | a0001c0003t0004g0044a0001c0003t0004g0045a0001c0003t0004g0046others(5): Show | 8 | HG00639.hp2 HG01884.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.161-9722G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169670328 | ||||||
chr4:169670384
|
A | G | 1 | a0001c0001t0052g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.161-9666A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169670384 | ||||||
chr4:169670464
|
C | T | 23 | a0001c0003t0004g0033a0001c0003t0004g0034a0001c0003t0004g0036others(20): Show | 23 | HG00639.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.161-9586C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169670464 | ||||||
chr4:169670491
|
C | T | 1 | a0001c0001t0052g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.161-9559C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169670491 | ||||||
chr4:169670494
|
T | G | 1 | a0001c0001t0042g0268 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.161-9556T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169670494 | ||||||
chr4:169670556
|
C | T | 1 | a0001c0001t0025g0002 | 2 | HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.161-9494C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169670556 | ||||||
chr4:169670595
|
C | T | 1 | a0001c0003t0004g0039 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.161-9455C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169670595 | ||||||
chr4:169670701
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.161-9349C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169670701 | ||||||
chr4:169670781
|
C | G | 1 | a0001c0001t0012g0259 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.161-9269C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169670781 | ||||||
chr4:169670871
|
A | C | 7 | a0001c0001t0011g0191a0001c0001t0011g0192a0001c0001t0011g0193others(4): Show | 7 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.161-9179A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169670871 | ||||||
chr4:169671147
|
C | T | 7 | a0001c0001t0011g0191a0001c0001t0011g0192a0001c0001t0011g0193others(4): Show | 7 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.161-8903C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169671147 | ||||||
chr4:169671303
|
T | A | 64 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0052others(61): Show | 66 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.161-8747T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169671303 | ||||||
chr4:169671489
|
A | G | 3 | a0001c0001t0015g0190a0001c0001t0015g0195a0001c0001t0015g0196 | 3 | HG02615.hp2 HG02630.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.161-8561A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169671489 | ||||||
chr4:169671583
|
C | A | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.161-8467C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169671583 | ||||||
chr4:169671759
|
G | T | 1 | a0001c0001t0007g0212 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.161-8291G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169671759 | ||||||
chr4:169671866
|
G | T | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.161-8184G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169671866 | ||||||
chr4:169671994
|
G | A | 64 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0052others(61): Show | 66 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.161-8056G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169671994 | ||||||
chr4:169672069
|
G | A | 1 | a0001c0001t0042g0268 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.161-7981G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169672069 | ||||||
chr4:169672073
|
G | A | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.161-7977G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169672073 | ||||||
chr4:169672076
|
G | T | 1 | a0001c0001t0042g0268 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.161-7974G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169672076 | ||||||
chr4:169672169
|
G | A | 3 | a0001c0003t0003g0016a0001c0003t0003g0017a0001c0003t0003g0018 | 3 | HG02886.hp1 HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.161-7881G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169672169 | ||||||
chr4:169672169
|
G | T | 1 | a0001c0001t0007g0212 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.161-7881G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169672169 | ||||||
chr4:169672218
|
A | G | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.161-7832A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169672218 | ||||||
chr4:169672220
|
T | TA | 6 | a0001c0003t0003g0021a0001c0003t0003g0269a0001c0003t0003g0271others(3): Show | 6 | HG01358.hp1 HG03516.hp2 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.161-7830_161-7829i others(3): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169672220 | ||||||
chr4:169672220
|
T | TAGATA | 13 | a0001c0003t0003g0001a0001c0003t0003g0013a0001c0003t0003g0016others(10): Show | 14 | HG02723.hp2 HG02886.hp2 HG02896.hp2 others(11): Show |
intron_variant | MODIFIER | c.161-7830_161-7829i others(7): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169672220 | ||||||
chr4:169672220
|
T | TAGATAGA others(2): Show |
14 | a0001c0003t0003g0003a0001c0003t0003g0017a0001c0003t0003g0019others(11): Show | 15 | HG01516.hp2 HG01517.hp1 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.161-7830_161-7829i others(11): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169672220 | ||||||
chr4:169672220
|
T | TAGATAGA others(6): Show |
12 | a0001c0003t0003g0018a0001c0003t0003g0020a0001c0003t0004g0037others(9): Show | 12 | HG00639.hp2 HG01175.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.161-7830_161-7829i others(15): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169672220 | ||||||
chr4:169672220
|
T | TAGATAGA others(10): Show |
1 | a0001c0003t0003g0027 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.161-7830_161-7829i others(19): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169672220 | ||||||
chr4:169672220
|
T | TGATA | 22 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(19): Show | 23 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.161-7793_161-7790d others(6): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169672220 | |||||
chr4:169672220
|
T | TGATAGAT others(1): Show |
43 | a0001c0001t0001g0126a0001c0001t0001g0128a0001c0001t0001g0133others(40): Show | 45 | HG00544.hp1 HG00558.hp1 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.161-7797_161-7790d others(10): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169672220 | |||||
chr4:169672220
|
T | TGATAGAT others(5): Show |
119 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0110others(116): Show | 120 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.161-7801_161-7790d others(14): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169672220 | |||||
chr4:169672220
|
T | TGATAGAT others(9): Show |
29 | a0001c0001t0001g0012a0001c0001t0001g0125a0001c0001t0001g0135others(26): Show | 29 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.161-7805_161-7790d others(18): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169672220 | |||||
chr4:169672220
|
T | TGATAGAT others(13): Show |
13 | a0001c0001t0001g0131a0001c0001t0011g0191a0001c0001t0011g0194others(10): Show | 13 | HG00140.hp2 HG00609.hp1 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.161-7809_161-7790d others(22): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169672220 | |||||
chr4:169672220
|
T | TGATAGAT others(17): Show |
2 | a0001c0001t0014g0229a0001c0002t0002g0101 | 2 | HG01099.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.161-7813_161-7790d others(26): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169672220 | |||||
chr4:169672431
|
C | T | 34 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(31): Show | 34 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.161-7619C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169672431 | ||||||
chr4:169672549
|
T | G | 1 | a0001c0001t0001g0120 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.161-7501T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169672549 | ||||||
chr4:169672653
|
TTTTGTTT others(5): Show |
T | 1 | a0001c0001t0001g0186 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.161-7385_161-7374d others(14): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169672653 | |||||
chr4:169672802
|
T | C | 7 | a0001c0001t0011g0191a0001c0001t0011g0192a0001c0001t0011g0193others(4): Show | 7 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.161-7248T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169672802 | ||||||
chr4:169672820
|
C | T | 3 | a0001c0001t0015g0190a0001c0001t0015g0195a0001c0001t0015g0196 | 3 | HG02615.hp2 HG02630.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.161-7230C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169672820 | ||||||
chr4:169672821
|
G | A | 1 | a0001c0001t0042g0268 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.161-7229G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169672821 | ||||||
chr4:169672895
|
C | T | 35 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.161-7155C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169672895 | ||||||
chr4:169672907
|
T | C | 271 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(268): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.161-7143T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169672907 | ||||||
chr4:169673044
|
T | C | 265 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(262): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.161-7006T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169673044 | ||||||
chr4:169673109
|
C | T | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.161-6941C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169673109 | ||||||
chr4:169673152
|
T | C | 4 | a0001c0003t0003g0016a0001c0003t0003g0017a0001c0003t0003g0018others(1): Show | 4 | HG02055.hp2 HG02886.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-6898T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169673152 | ||||||
chr4:169673177
|
A | G | 248 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(245): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.161-6873A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169673177 | ||||||
chr4:169673433
|
C | T | 8 | a0001c0001t0011g0191a0001c0001t0011g0192a0001c0001t0011g0193others(5): Show | 8 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.161-6617C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169673433 | ||||||
chr4:169673486
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.161-6564C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169673486 | ||||||
chr4:169673741
|
A | G | 64 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0052others(61): Show | 66 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.161-6309A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169673741 | ||||||
chr4:169673766
|
T | G | 2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | HG02109.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.161-6284T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169673766 | ||||||
chr4:169674040
|
A | G | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG00544.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.161-6010A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169674040 | ||||||
chr4:169674041
|
T | C | 3 | a0001c0001t0015g0190a0001c0001t0015g0195a0001c0001t0015g0196 | 3 | HG02615.hp2 HG02630.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.161-6009T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169674041 | ||||||
chr4:169674262
|
G | A | 13 | a0001c0003t0003g0003a0001c0003t0003g0013a0001c0003t0003g0019others(10): Show | 14 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.161-5788G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169674262 | ||||||
chr4:169674297
|
G | C | 3 | a0001c0003t0003g0013a0001c0003t0003g0023a0001c0003t0003g0024 | 3 | NA18982.hp1 NA18984.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.161-5753G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169674297 | ||||||
chr4:169674360
|
G | C | 1 | a0001c0003t0023g0035 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.161-5690G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169674360 | ||||||
chr4:169674483
|
T | G | 271 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(268): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.161-5567T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169674483 | ||||||
chr4:169674652
|
A | G | 64 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0052others(61): Show | 66 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.161-5398A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169674652 | ||||||
chr4:169674653
|
A | T | 35 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.161-5397A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169674653 | ||||||
chr4:169674774
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.161-5276C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169674774 | ||||||
chr4:169674931
|
G | A | 2 | a0001c0001t0033g0279a0001c0001t0045g0280 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.161-5119G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169674931 | ||||||
chr4:169674971
|
C | A | 248 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(245): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.161-5079C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169674971 | ||||||
chr4:169675021
|
C | T | 2 | a0001c0001t0025g0002a0001c0001t0034g0241 | 3 | HG02976.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.161-5029C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169675021 | ||||||
chr4:169675132
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.161-4918G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169675132 | ||||||
chr4:169675266
|
T | A | 1 | a0001c0001t0001g0160 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.161-4784T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169675266 | ||||||
chr4:169675429
|
G | C | 5 | a0001c0001t0005g0244a0001c0001t0005g0254a0001c0001t0005g0255others(2): Show | 5 | HG02055.hp1 HG02258.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-4621G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169675429 | ||||||
chr4:169675486
|
A | G | 1 | a0001c0001t0014g0234 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.161-4564A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169675486 | ||||||
chr4:169675528
|
C | T | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.161-4522C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169675528 | ||||||
chr4:169675877
|
A | G | 65 | a0001c0001t0001g0158a0001c0002t0002g0004a0001c0002t0002g0032others(62): Show | 67 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.161-4173A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169675877 | ||||||
chr4:169675902
|
G | A | 2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | HG02109.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.161-4148G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169675902 | ||||||
chr4:169675942
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.161-4108A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169675942 | ||||||
chr4:169676162
|
C | A | 1 | a0001c0001t0001g0274 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.161-3888C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169676162 | ||||||
chr4:169676280
|
A | T | 271 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(268): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.161-3770A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169676280 | ||||||
chr4:169676420
|
C | G | 1 | a0001c0001t0001g0150 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.161-3630C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169676420 | ||||||
chr4:169676512
|
C | CT | 64 | a0001c0001t0042g0268a0001c0002t0002g0004a0001c0002t0002g0032others(61): Show | 66 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.161-3527dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169676512 | |||||
chr4:169676512
|
CT | C | 35 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.161-3527delT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169676512 | |||||
chr4:169676569
|
C | T | 2 | a0001c0003t0020g0183a0001c0003t0020g0184 | 2 | HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.161-3481C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169676569 | ||||||
chr4:169676650
|
A | AT | 8 | a0001c0001t0001g0118a0001c0001t0001g0123a0001c0001t0001g0164others(5): Show | 8 | HG01175.hp1 HG02738.hp2 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.161-3381dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169676650 | |||||
chr4:169676650
|
AT | A | 56 | a0001c0001t0001g0113a0001c0001t0001g0128a0001c0001t0001g0130others(53): Show | 59 | HG00639.hp2 HG01175.hp2 HG01192.hp2 others(56): Show |
intron_variant | MODIFIER | c.161-3381delT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169676650 | |||||
chr4:169676650
|
ATT | A | 61 | a0001c0001t0042g0268a0001c0002t0002g0004a0001c0002t0002g0032others(58): Show | 63 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.161-3382_161-3381d others(4): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169676650 | |||||
chr4:169676670
|
G | C | 1 | a0001c0001t0045g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.161-3380G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169676670 | ||||||
chr4:169676821
|
A | G | 1 | a0001c0003t0037g0040 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.161-3229A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169676821 | ||||||
chr4:169676873
|
T | C | 1 | a0001c0001t0034g0241 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.161-3177T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169676873 | ||||||
chr4:169676997
|
G | A | 54 | a0001c0002t0002g0056a0001c0002t0002g0062a0001c0002t0002g0073others(51): Show | 56 | HG00639.hp2 HG01175.hp2 HG01346.hp1 others(53): Show |
intron_variant | MODIFIER | c.161-3053G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169676997 | ||||||
chr4:169677311
|
C | T | 2 | a0001c0001t0033g0279a0001c0001t0045g0280 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.161-2739C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169677311 | ||||||
chr4:169677431
|
T | G | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.161-2619T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169677431 | ||||||
chr4:169677590
|
A | C | 1 | a0001c0002t0008g0066 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.161-2460A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169677590 | ||||||
chr4:169677622
|
A | G | 12 | a0001c0003t0003g0003a0001c0003t0003g0013a0001c0003t0003g0019others(9): Show | 13 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.161-2428A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169677622 | ||||||
chr4:169677695
|
C | T | 1 | a0001c0001t0001g0168 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.161-2355C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169677695 | ||||||
chr4:169677835
|
C | G | 265 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(262): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.161-2215C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169677835 | ||||||
chr4:169677894
|
CT | C | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.161-2151delT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169677894 | |||||
chr4:169678280
|
C | A | 35 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.161-1770C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169678280 | ||||||
chr4:169678420
|
T | A | 1 | a0001c0001t0014g0234 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.161-1630T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169678420 | ||||||
chr4:169678558
|
C | T | 1 | a0001c0003t0003g0028 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.161-1492C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169678558 | ||||||
chr4:169678813
|
C | T | 1 | a0001c0001t0042g0268 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.161-1237C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169678813 | ||||||
chr4:169678860
|
T | C | 1 | a0001c0001t0043g0260 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.161-1190T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169678860 | ||||||
chr4:169678861
|
A | C | 1 | a0001c0001t0043g0260 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.161-1189A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169678861 | ||||||
chr4:169678869
|
T | C | 1 | a0001c0001t0043g0260 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.161-1181T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169678869 | ||||||
chr4:169678878
|
T | C | 1 | a0001c0001t0043g0260 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.161-1172T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169678878 | ||||||
chr4:169678879
|
G | C | 1 | a0001c0001t0043g0260 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.161-1171G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169678879 | ||||||
chr4:169678887
|
T | C | 1 | a0001c0001t0043g0260 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.161-1163T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169678887 | ||||||
chr4:169678893
|
C | T | 1 | a0001c0001t0043g0260 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.161-1157C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169678893 | ||||||
chr4:169678894
|
C | G | 1 | a0001c0001t0043g0260 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.161-1156C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169678894 | ||||||
chr4:169678898
|
C | T | 1 | a0001c0001t0043g0260 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.161-1152C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169678898 | ||||||
chr4:169678987
|
GCCGGGCG others(17): Show |
G | 2 | a0001c0001t0033g0279a0001c0001t0045g0280 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.161-1060_161-1037d others(26): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169678987 | |||||
chr4:169678989
|
C | T | 1 | a0001c0001t0001g0133 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.161-1061C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169678989 | ||||||
chr4:169678993
|
C | A | 94 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(91): Show | 95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.161-1057C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169678993 | ||||||
chr4:169679070
|
C | T | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.161-980C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679070 | ||||||
chr4:169679076
|
C | A | 9 | a0001c0001t0006g0197a0001c0001t0006g0198a0001c0001t0006g0199others(6): Show | 9 | HG01884.hp1 HG02572.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.161-974C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679076 | ||||||
chr4:169679085
|
C | T | 1 | a0001c0001t0012g0259 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.161-965C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679085 | ||||||
chr4:169679124
|
A | G | 3 | a0001c0003t0004g0034a0001c0003t0004g0036a0001c0003t0023g0035 | 3 | HG02486.hp1 HG02723.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.161-926A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679124 | ||||||
chr4:169679140
|
C | T | 1 | a0001c0003t0003g0026 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.161-910C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679140 | ||||||
chr4:169679141
|
G | C | 1 | a0001c0003t0003g0026 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.161-909G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679141 | ||||||
chr4:169679152
|
G | C | 1 | a0001c0001t0006g0202 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.161-898G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679152 | ||||||
chr4:169679181
|
G | A | 35 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.161-869G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679181 | ||||||
chr4:169679182
|
C | T | 1 | a0001c0002t0002g0102 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.161-868C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679182 | ||||||
chr4:169679253
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.161-797G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679253 | ||||||
chr4:169679310
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.161-740G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679310 | ||||||
chr4:169679318
|
C | T | 34 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(31): Show | 34 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.161-732C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679318 | ||||||
chr4:169679327
|
C | CGGGATGG others(33): Show |
5 | a0001c0001t0001g0133a0001c0001t0001g0137a0001c0001t0001g0139others(2): Show | 5 | HG02129.hp1 NA18747.hp2 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.161-711_161-672dup others(40): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169679327 | |||||
chr4:169679335
|
C | T | 1 | a0001c0001t0042g0268 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.161-715C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679335 | ||||||
chr4:169679387
|
G | A | 35 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.161-663G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679387 | ||||||
chr4:169679483
|
C | CG | 7 | a0001c0001t0001g0159a0001c0001t0005g0253a0001c0001t0010g0216others(4): Show | 7 | HG01109.hp1 HG01255.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.161-563dupG | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169679483 | |||||
chr4:169679496
|
G | A | 1 | a0001c0002t0002g0075 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.161-554G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679496 | ||||||
chr4:169679565
|
G | C | 1 | a0001c0003t0003g0029 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.161-485G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679565 | ||||||
chr4:169679654
|
C | T | 35 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.161-396C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679654 | ||||||
chr4:169679672
|
C | G | 7 | a0001c0003t0003g0001a0001c0003t0003g0269a0001c0003t0003g0271others(4): Show | 8 | HG02280.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.161-378C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679672 | ||||||
chr4:169679681
|
G | T | 35 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.161-369G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679681 | ||||||
chr4:169679772
|
C | G | 1 | a0001c0001t0001g0133 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.161-278C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679772 | ||||||
chr4:169679782
|
C | T | 1 | a0001c0002t0009g0098 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.161-268C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679782 | ||||||
chr4:169679783
|
G | C | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG02257.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.161-267G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679783 | ||||||
chr4:169679835
|
C | T | 1 | a0001c0003t0040g0278 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.161-215C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679835 | ||||||
chr4:169679863
|
AGGGAGAC others(33): Show |
A | 59 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0052others(56): Show | 61 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.161-172_161-133del others(40): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169679863 | |||||
chr4:169679887
|
C | T | 2 | a0001c0001t0033g0279a0001c0001t0045g0280 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.161-163C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679887 | ||||||
chr4:169679893
|
C | T | 1 | a0001c0003t0003g0277 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.161-157C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679893 | ||||||
chr4:169680021
|
A | G | 34 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(31): Show | 34 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.161-29A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169680021 | ||||||
chr4:169680298
|
T | C | 54 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0052others(51): Show | 56 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.318+91T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169680298 | ||||||
chr4:169680507
|
A | G | 3 | a0001c0001t0007g0227a0001c0001t0007g0235a0001c0001t0028g0221 | 3 | HG00140.hp1 HG01109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.318+300A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169680507 | ||||||
chr4:169680672
|
C | T | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.318+465C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169680672 | ||||||
chr4:169680757
|
G | C | 1 | a0001c0001t0047g0210 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.318+550G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169680757 | ||||||
chr4:169680777
|
A | C | 1 | a0001c0003t0003g0029 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.318+570A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169680777 | ||||||
chr4:169680804
|
C | T | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.318+597C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169680804 | ||||||
chr4:169680821
|
A | G | 258 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(255): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.318+614A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169680821 | ||||||
chr4:169680835
|
A | G | 9 | a0001c0003t0004g0033a0001c0003t0004g0044a0001c0003t0004g0045others(6): Show | 9 | HG00639.hp2 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.318+628A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169680835 | ||||||
chr4:169680924
|
C | T | 2 | a0001c0001t0001g0155a0001c0001t0001g0171 | 2 | HG01074.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.318+717C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169680924 | ||||||
chr4:169681031
|
C | A | 2 | a0001c0001t0033g0279a0001c0001t0045g0280 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.318+824C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169681031 | ||||||
chr4:169681045
|
C | T | 2 | a0001c0001t0025g0002a0001c0001t0034g0241 | 3 | HG02976.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.318+838C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169681045 | ||||||
chr4:169681072
|
C | T | 61 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(58): Show | 63 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.318+865C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169681072 | ||||||
chr4:169681073
|
G | A | 64 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0052others(61): Show | 66 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.318+866G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169681073 | ||||||
chr4:169681116
|
T | G | 1 | a0001c0001t0001g0129 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.318+909T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169681116 | ||||||
chr4:169681245
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.318+1038G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169681245 | ||||||
chr4:169681273
|
C | T | 2 | a0001c0001t0001g0118a0001c0001t0001g0129 | 2 | HG00280.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.318+1066C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169681273 | ||||||
chr4:169681347
|
C | T | 4 | a0001c0003t0003g0016a0001c0003t0003g0017a0001c0003t0003g0018others(1): Show | 4 | HG02055.hp2 HG02886.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.318+1140C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169681347 | ||||||
chr4:169681348
|
A | G | 64 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0052others(61): Show | 66 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.318+1141A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169681348 | ||||||
chr4:169681416
|
T | G | 3 | a0001c0001t0001g0113a0001c0001t0001g0130a0001c0001t0001g0131 | 3 | NA19068.hp2 NA19078.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.318+1209T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169681416 | ||||||
chr4:169681573
|
A | G | 1 | a0001c0001t0016g0211 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.318+1366A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169681573 | ||||||
chr4:169681706
|
T | A | 25 | a0001c0001t0025g0002a0001c0003t0003g0001a0001c0003t0003g0003others(22): Show | 28 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(25): Show |
intron_variant | MODIFIER | c.318+1499T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169681706 | ||||||
chr4:169682038
|
G | A | 265 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(262): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.318+1831G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169682038 | ||||||
chr4:169682215
|
TATATA | T | 3 | a0001c0001t0033g0279a0001c0001t0045g0280a0001c0003t0003g0277 | 3 | HG03139.hp1 HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.318+2017_318+2021d others(7): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 169682215 | |||||
chr4:169682255
|
A | G | 6 | a0001c0001t0001g0007a0001c0001t0001g0119a0001c0001t0001g0154others(3): Show | 6 | HG01099.hp2 HG01258.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.318+2048A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169682255 | ||||||
chr4:169682291
|
A | G | 5 | a0001c0002t0002g0059a0001c0002t0002g0082a0001c0002t0002g0083others(2): Show | 5 | HG01192.hp2 HG01243.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.318+2084A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169682291 | ||||||
chr4:169682368
|
A | G | 8 | a0001c0001t0011g0191a0001c0001t0011g0192a0001c0001t0011g0193others(5): Show | 8 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.318+2161A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169682368 | ||||||
chr4:169682372
|
T | C | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.318+2165T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169682372 | ||||||
chr4:169682485
|
C | G | 2 | a0001c0001t0025g0002a0001c0001t0034g0241 | 3 | HG02976.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.318+2278C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169682485 | ||||||
chr4:169682550
|
C | T | 2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | HG02109.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.318+2343C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169682550 | ||||||
chr4:169682828
|
A | G | 1 | a0001c0001t0001g0114 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.318+2621A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169682828 | ||||||
chr4:169682908
|
A | G | 3 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0007t0001g0162 | 3 | HG00642.hp1 HG00733.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.318+2701A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169682908 | ||||||
chr4:169683435
|
C | T | 3 | a0001c0003t0003g0016a0001c0003t0003g0017a0001c0003t0003g0018 | 3 | HG02886.hp1 HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.318+3228C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169683435 | ||||||
chr4:169683657
|
A | G | 1 | a0001c0003t0003g0020 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.318+3450A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169683657 | ||||||
chr4:169683679
|
G | A | 270 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(267): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.318+3472G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169683679 | ||||||
chr4:169683744
|
A | AT | 16 | a0001c0001t0001g0135a0001c0001t0001g0276a0001c0001t0006g0197others(13): Show | 17 | HG01516.hp2 HG01517.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.318+3555dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 169683744 | |||||
chr4:169683744
|
AT | A | 7 | a0001c0001t0001g0138a0001c0001t0001g0145a0001c0001t0001g0148others(4): Show | 7 | HG01257.hp2 HG02965.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.318+3555delT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 169683744 | |||||
chr4:169683765
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.318+3558G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169683765 | ||||||
chr4:169683772
|
C | G | 8 | a0001c0001t0011g0191a0001c0001t0011g0192a0001c0001t0011g0193others(5): Show | 8 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.318+3565C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169683772 | ||||||
chr4:169683912
|
T | G | 4 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0032g0185others(1): Show | 4 | HG00099.hp2 HG00642.hp1 HG00733.hp1 others(1): Show |
intron_variant | MODIFIER | c.318+3705T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169683912 | ||||||
chr4:169683959
|
T | G | 4 | a0001c0001t0006g0197a0001c0001t0006g0199a0001c0001t0006g0200others(1): Show | 4 | HG01884.hp1 HG02572.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.319-3699T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169683959 | ||||||
chr4:169683971
|
G | A | 11 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0006g0197others(8): Show | 11 | HG01884.hp1 HG02572.hp2 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.319-3687G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169683971 | ||||||
chr4:169684266
|
T | C | 2 | a0001c0001t0001g0182a0001c0001t0001g0186 | 2 | HG00609.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.319-3392T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169684266 | ||||||
chr4:169684387
|
G | A | 64 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0052others(61): Show | 66 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.319-3271G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169684387 | ||||||
chr4:169684561
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.319-3097T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169684561 | ||||||
chr4:169684637
|
T | C | 7 | a0001c0003t0003g0001a0001c0003t0003g0269a0001c0003t0003g0271others(4): Show | 8 | HG02280.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.319-3021T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169684637 | ||||||
chr4:169684814
|
A | G | 2 | a0001c0001t0018g0170a0001c0001t0018g0172 | 2 | HG00323.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.319-2844A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169684814 | ||||||
chr4:169684826
|
C | A | 1 | a0001c0001t0001g0179 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.319-2832C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169684826 | ||||||
chr4:169684877
|
A | G | 99 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(96): Show | 101 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.319-2781A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169684877 | ||||||
chr4:169684971
|
G | C | 34 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(31): Show | 34 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.319-2687G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169684971 | ||||||
chr4:169684975
|
A | AT | 17 | a0001c0001t0005g0244a0001c0001t0005g0255a0001c0001t0011g0191others(14): Show | 17 | HG02055.hp1 HG02055.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.319-2660dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 169684975 | |||||
chr4:169684975
|
AT | A | 156 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(153): Show | 161 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.319-2660delT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 169684975 | |||||
chr4:169684975
|
ATT | A | 18 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0116others(15): Show | 18 | HG00639.hp1 HG01069.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.319-2661_319-2660d others(4): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 169684975 | |||||
chr4:169684985
|
T | C | 1 | a0001c0002t0002g0109 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.319-2673T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169684985 | ||||||
chr4:169685191
|
G | T | 1 | a0001c0004t0002g0065 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.319-2467G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169685191 | ||||||
chr4:169685193
|
G | A | 3 | a0001c0001t0012g0262a0001c0001t0012g0264a0002c0005t0012g0263 | 3 | HG03540.hp1 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.319-2465G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169685193 | ||||||
chr4:169685306
|
C | T | 21 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(18): Show | 23 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(20): Show |
intron_variant | MODIFIER | c.319-2352C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169685306 | ||||||
chr4:169685368
|
C | A | 1 | a0001c0001t0001g0163 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.319-2290C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169685368 | ||||||
chr4:169685436
|
T | C | 1 | a0001c0001t0042g0268 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.319-2222T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169685436 | ||||||
chr4:169685472
|
C | G | 1 | a0001c0002t0017g0157 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.319-2186C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169685472 | ||||||
chr4:169685638
|
G | A | 1 | a0001c0001t0034g0241 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.319-2020G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169685638 | ||||||
chr4:169685645
|
A | G | 1 | a0001c0001t0006g0267 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.319-2013A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169685645 | ||||||
chr4:169685675
|
C | T | 5 | a0001c0003t0003g0001a0001c0003t0003g0269a0001c0003t0003g0271others(2): Show | 6 | HG02896.hp2 HG02897.hp1 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.319-1983C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169685675 | ||||||
chr4:169685681
|
A | G | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.319-1977A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169685681 | ||||||
chr4:169685780
|
TATC | T | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.319-1875_319-1873d others(5): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 169685780 | |||||
chr4:169685925
|
G | A | 54 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0052others(51): Show | 56 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.319-1733G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169685925 | ||||||
chr4:169685987
|
C | T | 2 | a0001c0003t0020g0183a0001c0003t0020g0184 | 2 | HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.319-1671C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169685987 | ||||||
chr4:169686006
|
G | A | 90 | a0001c0001t0033g0279a0001c0001t0042g0268a0001c0001t0045g0280others(87): Show | 92 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.319-1652G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169686006 | ||||||
chr4:169686059
|
A | G | 7 | a0001c0001t0011g0191a0001c0001t0011g0192a0001c0001t0011g0193others(4): Show | 7 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.319-1599A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169686059 | ||||||
chr4:169686251
|
A | T | 1 | a0001c0003t0004g0041 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.319-1407A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169686251 | ||||||
chr4:169686269
|
A | G | 1 | a0001c0001t0006g0198 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.319-1389A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169686269 | ||||||
chr4:169686419
|
C | CT | 63 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0052others(60): Show | 65 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.319-1224dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 169686419 | |||||
chr4:169686437
|
G | T | 2 | a0001c0001t0033g0279a0001c0001t0045g0280 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.319-1221G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169686437 | ||||||
chr4:169686529
|
G | T | 1 | a0001c0001t0014g0230 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.319-1129G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169686529 | ||||||
chr4:169686555
|
T | TA | 3 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0007t0001g0162 | 3 | HG00642.hp1 HG00733.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.319-1102dupA | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 169686555 | |||||
chr4:169686565
|
C | T | 35 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.319-1093C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169686565 | ||||||
chr4:169686596
|
T | C | 1 | a0001c0003t0040g0278 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.319-1062T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169686596 | ||||||
chr4:169686652
|
T | G | 1 | a0001c0001t0001g0118 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.319-1006T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169686652 | ||||||
chr4:169686695
|
G | A | 1 | a0001c0001t0016g0219 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.319-963G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169686695 | ||||||
chr4:169686882
|
T | C | 47 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(44): Show | 49 | HG00639.hp2 HG01175.hp2 HG01346.hp1 others(46): Show |
intron_variant | MODIFIER | c.319-776T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169686882 | ||||||
chr4:169686884
|
A | G | 47 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(44): Show | 49 | HG00639.hp2 HG01175.hp2 HG01346.hp1 others(46): Show |
intron_variant | MODIFIER | c.319-774A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169686884 | ||||||
chr4:169687246
|
T | A | 64 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0052others(61): Show | 66 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.319-412T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169687246 | ||||||
chr4:169687331
|
A | T | 7 | a0001c0001t0011g0191a0001c0001t0011g0192a0001c0001t0011g0193others(4): Show | 7 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.319-327A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169687331 | ||||||
chr4:169687431
|
T | A | 53 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0052others(50): Show | 55 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.319-227T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169687431 | ||||||
chr4:169687829
|
A | G | 23 | a0001c0003t0004g0033a0001c0003t0004g0034a0001c0003t0004g0036others(20): Show | 23 | HG00639.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.418+72A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 4/12 | chr4 | 169687829 | ||||||
chr4:169687985
|
G | C | 1 | a0001c0001t0012g0259 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.418+228G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 4/12 | chr4 | 169687985 | ||||||
chr4:169688070
|
T | C | 1 | a0001c0001t0034g0241 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.418+313T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 4/12 | chr4 | 169688070 | ||||||
chr4:169688100
|
T | C | 24 | a0001c0002t0008g0066a0001c0003t0004g0033a0001c0003t0004g0034others(21): Show | 24 | HG00639.hp2 HG01175.hp2 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.418+343T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 4/12 | chr4 | 169688100 | ||||||
chr4:169688130
|
T | C | 1 | a0001c0001t0005g0244 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.418+373T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 4/12 | chr4 | 169688130 | ||||||
chr4:169688158
|
T | G | 3 | a0001c0002t0002g0058a0001c0002t0002g0072a0001c0002t0002g0080 | 3 | NA18947.hp2 NA18981.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.418+401T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 4/12 | chr4 | 169688158 | ||||||
chr4:169688295
|
C | T | 2 | a0001c0003t0004g0036a0001c0003t0023g0035 | 2 | HG02723.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.418+538C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 4/12 | chr4 | 169688295 | ||||||
chr4:169688363
|
T | C | 64 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0052others(61): Show | 66 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.418+606T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 4/12 | chr4 | 169688363 | ||||||
chr4:169688413
|
A | T | 9 | a0001c0001t0006g0197a0001c0001t0006g0198a0001c0001t0006g0199others(6): Show | 9 | HG01884.hp1 HG02572.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.419-630A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 4/12 | chr4 | 169688413 | ||||||
chr4:169688568
|
G | T | 1 | a0001c0001t0042g0268 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.419-475G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 4/12 | chr4 | 169688568 | ||||||
chr4:169688910
|
T | G | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.419-133T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 4/12 | chr4 | 169688910 | ||||||
chr4:169689473
|
T | C | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.606+243T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 5/12 | chr4 | 169689473 | ||||||
chr4:169689581
|
A | G | 1 | a0001c0002t0002g0054 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.606+351A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 5/12 | chr4 | 169689581 | ||||||
chr4:169689659
|
G | A | 249 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(246): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.606+429G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 5/12 | chr4 | 169689659 | ||||||
chr4:169689724
|
A | G | 64 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0052others(61): Show | 66 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.606+494A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 5/12 | chr4 | 169689724 | ||||||
chr4:169689728
|
T | C | 1 | a0001c0003t0004g0034 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.606+498T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 5/12 | chr4 | 169689728 | ||||||
chr4:169690137
|
C | CT | 237 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(234): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.607-374dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 169690137 | |||||
chr4:169690137
|
C | CTT | 20 | a0001c0001t0001g0265a0001c0001t0006g0197a0001c0001t0006g0198others(17): Show | 20 | HG01884.hp1 HG01981.hp2 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.607-375_607-374dup others(2): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 169690137 | |||||
chr4:169690370
|
T | C | 7 | a0001c0003t0003g0001a0001c0003t0003g0269a0001c0003t0003g0271others(4): Show | 8 | HG02280.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.607-160T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 5/12 | chr4 | 169690370 | ||||||
chr4:169690391
|
C | G | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.607-139C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 5/12 | chr4 | 169690391 | ||||||
chr4:169690719
|
A | G | 1 | a0001c0003t0003g0019 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.729+67A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 6/12 | chr4 | 169690719 | ||||||
chr4:169690739
|
G | A | 1 | a0001c0001t0012g0259 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.729+87G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 6/12 | chr4 | 169690739 | ||||||
chr4:169690777
|
T | A | 1 | a0001c0001t0034g0241 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.729+125T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 6/12 | chr4 | 169690777 | ||||||
chr4:169690830
|
A | G | 94 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(91): Show | 95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.729+178A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 6/12 | chr4 | 169690830 | ||||||
chr4:169690928
|
C | A | 1 | a0001c0001t0001g0012 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.729+276C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 6/12 | chr4 | 169690928 | ||||||
chr4:169691012
|
T | TG | 5 | a0001c0002t0009g0053a0001c0002t0009g0096a0001c0002t0009g0097others(2): Show | 5 | HG02109.hp2 HG02451.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.729+360_729+361ins others(1): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 6/12 | chr4 | 169691012 | ||||||
chr4:169691037
|
C | T | 1 | a0001c0001t0006g0199 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.729+385C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 6/12 | chr4 | 169691037 | ||||||
chr4:169691087
|
G | A | 63 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0052others(60): Show | 65 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.729+435G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 6/12 | chr4 | 169691087 | ||||||
chr4:169691185
|
G | T | 1 | a0001c0001t0031g0242 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.729+533G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 6/12 | chr4 | 169691185 | ||||||
chr4:169691189
|
T | G | 47 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(44): Show | 49 | HG00639.hp2 HG01175.hp2 HG01346.hp1 others(46): Show |
intron_variant | MODIFIER | c.729+537T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 6/12 | chr4 | 169691189 | ||||||
chr4:169691193
|
T | G | 7 | a0001c0003t0003g0001a0001c0003t0003g0269a0001c0003t0003g0271others(4): Show | 8 | HG02280.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.729+541T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 6/12 | chr4 | 169691193 | ||||||
chr4:169691524
|
T | G | 1 | a0001c0001t0001g0164 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.730-590T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 6/12 | chr4 | 169691524 | ||||||
chr4:169691608
|
G | A | 2 | a0001c0001t0033g0279a0001c0001t0045g0280 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.730-506G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 6/12 | chr4 | 169691608 | ||||||
chr4:169691663
|
C | T | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.730-451C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 6/12 | chr4 | 169691663 | ||||||
chr4:169691837
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.730-277A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 6/12 | chr4 | 169691837 | ||||||
chr4:169692017
|
A | G | 1 | a0001c0001t0005g0258 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.730-97A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 6/12 | chr4 | 169692017 | ||||||
chr4:169692926
|
A | G | 1 | a0001c0001t0035g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.936+606A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169692926 | ||||||
chr4:169692934
|
T | C | 4 | a0001c0003t0003g0016a0001c0003t0003g0017a0001c0003t0003g0018others(1): Show | 4 | HG02055.hp2 HG02886.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.936+614T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169692934 | ||||||
chr4:169692988
|
A | G | 1 | a0001c0001t0025g0002 | 2 | HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.936+668A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169692988 | ||||||
chr4:169693054
|
G | A | 3 | a0001c0003t0003g0016a0001c0003t0003g0017a0001c0003t0003g0018 | 3 | HG02886.hp1 HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.936+734G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169693054 | ||||||
chr4:169693581
|
AT | A | 54 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0052others(51): Show | 56 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.936+1263delT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 169693581 | |||||
chr4:169693899
|
G | A | 1 | a0001c0002t0002g0064 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.936+1579G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169693899 | ||||||
chr4:169693944
|
G | A | 2 | a0001c0003t0020g0183a0001c0003t0020g0184 | 2 | HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.936+1624G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169693944 | ||||||
chr4:169694182
|
A | G | 94 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(91): Show | 95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.937-1430A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169694182 | ||||||
chr4:169694197
|
C | T | 271 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(268): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.937-1415C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169694197 | ||||||
chr4:169694274
|
A | C | 2 | a0001c0001t0033g0279a0001c0001t0045g0280 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.937-1338A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169694274 | ||||||
chr4:169694352
|
C | T | 94 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(91): Show | 95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.937-1260C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169694352 | ||||||
chr4:169694372
|
G | C | 23 | a0001c0003t0004g0033a0001c0003t0004g0034a0001c0003t0004g0036others(20): Show | 23 | HG00639.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.937-1240G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169694372 | ||||||
chr4:169694386
|
A | G | 1 | a0001c0003t0004g0034 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.937-1226A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169694386 | ||||||
chr4:169694500
|
C | A | 7 | a0001c0002t0002g0061a0001c0002t0002g0077a0001c0002t0002g0090others(4): Show | 7 | HG00558.hp1 HG02155.hp2 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.937-1112C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169694500 | ||||||
chr4:169694700
|
G | A | 34 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(31): Show | 34 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.937-912G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169694700 | ||||||
chr4:169694711
|
C | T | 1 | a0001c0001t0006g0199 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.937-901C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169694711 | ||||||
chr4:169694818
|
A | G | 265 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(262): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.937-794A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169694818 | ||||||
chr4:169695054
|
A | G | 2 | a0001c0003t0004g0034a0001c0003t0004g0036 | 2 | HG02486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.937-558A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169695054 | ||||||
chr4:169695314
|
C | T | 94 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(91): Show | 95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.937-298C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169695314 | ||||||
chr4:169695346
|
T | C | 1 | a0001c0001t0024g0218 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.937-266T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169695346 | ||||||
chr4:169695423
|
A | C | 1 | a0001c0001t0035g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.937-189A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169695423 | ||||||
chr4:169695424
|
A | G | 2 | a0001c0001t0033g0279a0001c0001t0045g0280 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.937-188A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169695424 | ||||||
chr4:169695564
|
T | C | 23 | a0001c0003t0004g0033a0001c0003t0004g0034a0001c0003t0004g0036others(20): Show | 23 | HG00639.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.937-48T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169695564 | ||||||
chr4:169695767
|
G | A | 271 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(268): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.1017+75G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 8/12 | chr4 | 169695767 | ||||||
chr4:169695924
|
A | G | 9 | a0001c0001t0006g0197a0001c0001t0006g0198a0001c0001t0006g0199others(6): Show | 9 | HG01884.hp1 HG02572.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.1017+232A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 8/12 | chr4 | 169695924 | ||||||
chr4:169695957
|
G | A | 3 | a0001c0003t0003g0013a0001c0003t0003g0023a0001c0003t0003g0024 | 3 | NA18982.hp1 NA18984.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1017+265G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 8/12 | chr4 | 169695957 | ||||||
chr4:169696003
|
A | G | 64 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0052others(61): Show | 66 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.1017+311A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 8/12 | chr4 | 169696003 | ||||||
chr4:169696095
|
G | T | 1 | a0001c0003t0023g0035 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1017+403G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 8/12 | chr4 | 169696095 | ||||||
chr4:169696176
|
G | A | 2 | a0001c0001t0001g0182a0001c0001t0001g0186 | 2 | HG00609.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1017+484G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 8/12 | chr4 | 169696176 | ||||||
chr4:169696180
|
C | T | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0129 | 3 | HG00280.hp2 HG01175.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.1017+488C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 8/12 | chr4 | 169696180 | ||||||
chr4:169696613
|
C | T | 1 | a0001c0001t0034g0241 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1018-576C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 8/12 | chr4 | 169696613 | ||||||
chr4:169696626
|
A | G | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.1018-563A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 8/12 | chr4 | 169696626 | ||||||
chr4:169696819
|
T | TC | 47 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(44): Show | 49 | HG00639.hp2 HG01175.hp2 HG01346.hp1 others(46): Show |
intron_variant | MODIFIER | c.1018-370_1018-369i others(3): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 8/12 | chr4 | 169696819 | ||||||
chr4:169696907
|
A | T | 4 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275others(1): Show | 4 | HG02622.hp1 HG02630.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1018-282A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 8/12 | chr4 | 169696907 | ||||||
chr4:169698037
|
T | C | 1 | a0001c0001t0001g0012 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1563+303T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169698037 | ||||||
chr4:169698246
|
A | G | 1 | a0001c0001t0005g0258 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1563+512A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169698246 | ||||||
chr4:169698365
|
A | G | 3 | a0001c0001t0001g0149a0001c0001t0001g0153a0001c0001t0001g0167 | 3 | HG00558.hp2 HG02040.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1563+631A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169698365 | ||||||
chr4:169698398
|
G | A | 1 | a0001c0002t0008g0066 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1563+664G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169698398 | ||||||
chr4:169698419
|
C | T | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0129 | 3 | HG00280.hp2 HG01175.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.1563+685C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169698419 | ||||||
chr4:169698526
|
C | A | 4 | a0001c0001t0012g0259a0001c0001t0012g0262a0001c0001t0012g0264others(1): Show | 4 | HG02486.hp2 HG03540.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1563+792C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169698526 | ||||||
chr4:169698734
|
T | C | 26 | a0001c0002t0002g0004a0001c0002t0002g0052a0001c0002t0002g0056others(23): Show | 27 | HG00597.hp1 HG00609.hp1 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.1563+1000T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169698734 | ||||||
chr4:169699030
|
TCTC | T | 3 | a0001c0002t0002g0057a0001c0002t0002g0079a0001c0002t0041g0100 | 3 | HG00140.hp2 HG01106.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1563+1299_1563+130 others(7): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 169699030 | |||||
chr4:169699099
|
G | A | 3 | a0001c0001t0001g0181a0001c0001t0001g0265a0001c0001t0001g0266 | 3 | NA18981.hp2 NA18986.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1563+1365G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169699099 | ||||||
chr4:169699377
|
G | A | 1 | a0001c0001t0042g0268 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1563+1643G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169699377 | ||||||
chr4:169699661
|
A | G | 68 | a0001c0001t0033g0279a0001c0001t0042g0268a0001c0001t0045g0280others(65): Show | 70 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.1563+1927A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169699661 | ||||||
chr4:169699720
|
A | G | 7 | a0001c0003t0003g0001a0001c0003t0003g0269a0001c0003t0003g0271others(4): Show | 8 | HG02280.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1563+1986A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169699720 | ||||||
chr4:169699775
|
G | A | 17 | a0001c0003t0003g0003a0001c0003t0003g0013a0001c0003t0003g0016others(14): Show | 18 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(15): Show |
intron_variant | MODIFIER | c.1563+2041G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169699775 | ||||||
chr4:169699874
|
A | G | 1 | a0001c0003t0003g0026 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1563+2140A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169699874 | ||||||
chr4:169699894
|
T | G | 69 | a0001c0001t0001g0239a0001c0001t0015g0190a0001c0001t0015g0195others(66): Show | 71 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.1563+2160T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169699894 | ||||||
chr4:169699997
|
G | T | 1 | a0001c0001t0035g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1563+2263G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169699997 | ||||||
chr4:169700081
|
C | T | 35 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.1563+2347C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169700081 | ||||||
chr4:169700252
|
A | AGTTT | 150 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(147): Show | 154 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1563+2522_1563+252 others(8): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 169700252 | |||||
chr4:169700536
|
A | G | 9 | a0001c0001t0006g0197a0001c0001t0006g0198a0001c0001t0006g0199others(6): Show | 9 | HG01884.hp1 HG02572.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.1563+2802A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169700536 | ||||||
chr4:169700817
|
G | A | 1 | a0001c0001t0034g0241 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1563+3083G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169700817 | ||||||
chr4:169700822
|
A | G | 92 | a0001c0001t0025g0002a0001c0001t0033g0279a0001c0001t0042g0268others(89): Show | 95 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.1563+3088A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169700822 | ||||||
chr4:169700890
|
G | T | 2 | a0001c0001t0033g0279a0001c0001t0045g0280 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1564-3108G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169700890 | ||||||
chr4:169700906
|
G | T | 4 | a0001c0003t0003g0016a0001c0003t0003g0017a0001c0003t0003g0018others(1): Show | 4 | HG02055.hp2 HG02886.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1564-3092G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169700906 | ||||||
chr4:169701042
|
CTCTGTAG others(2): Show |
C | 3 | a0001c0003t0003g0013a0001c0003t0003g0023a0001c0003t0003g0024 | 3 | NA18982.hp1 NA18984.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1564-2954_1564-294 others(13): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 169701042 | |||||
chr4:169701044
|
CTGTAGCA | C | 21 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0016others(18): Show | 23 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(20): Show |
intron_variant | MODIFIER | c.1564-2950_1564-294 others(11): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 169701044 | |||||
chr4:169701071
|
A | C | 1 | a0001c0002t0017g0005 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1564-2927A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169701071 | ||||||
chr4:169701278
|
T | A | 7 | a0001c0002t0002g0056a0001c0002t0002g0062a0001c0002t0002g0073others(4): Show | 7 | NA18940.hp2 NA18943.hp2 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.1564-2720T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169701278 | ||||||
chr4:169701344
|
T | G | 2 | a0001c0001t0001g0155a0001c0001t0001g0171 | 2 | HG01074.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.1564-2654T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169701344 | ||||||
chr4:169701453
|
C | A | 1 | a0001c0001t0001g0239 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1564-2545C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169701453 | ||||||
chr4:169701773
|
C | T | 1 | a0001c0001t0001g0110 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1564-2225C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169701773 | ||||||
chr4:169701850
|
A | G | 3 | a0001c0003t0003g0013a0001c0003t0003g0023a0001c0003t0003g0024 | 3 | NA18982.hp1 NA18984.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1564-2148A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169701850 | ||||||
chr4:169702068
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1564-1930G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169702068 | ||||||
chr4:169702076
|
C | T | 1 | a0001c0002t0041g0100 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1564-1922C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169702076 | ||||||
chr4:169702083
|
C | T | 3 | a0001c0001t0015g0190a0001c0001t0015g0195a0001c0001t0015g0196 | 3 | HG02615.hp2 HG02630.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1564-1915C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169702083 | ||||||
chr4:169702087
|
C | T | 1 | a0001c0001t0010g0224 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1564-1911C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169702087 | ||||||
chr4:169702091
|
C | A | 1 | a0001c0003t0004g0043 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1564-1907C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169702091 | ||||||
chr4:169702142
|
G | T | 3 | a0001c0001t0005g0256a0001c0001t0005g0257a0001c0001t0005g0258 | 3 | HG02622.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1564-1856G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169702142 | ||||||
chr4:169702403
|
G | A | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.1564-1595G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169702403 | ||||||
chr4:169702679
|
C | T | 6 | a0001c0001t0005g0246a0001c0001t0005g0247a0001c0001t0005g0249others(3): Show | 6 | HG01109.hp1 HG02258.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1564-1319C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169702679 | ||||||
chr4:169702777
|
C | CA | 24 | a0001c0001t0011g0191a0001c0001t0012g0262a0001c0001t0024g0218others(21): Show | 25 | HG01346.hp1 HG01981.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1564-1201dupA | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 169702777 | |||||
chr4:169702777
|
C | CAA | 58 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(55): Show | 60 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.1564-1202_1564-120 others(6): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 169702777 | |||||
chr4:169702777
|
CAAAAAAA others(5): Show |
C | 93 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(90): Show | 94 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.1564-1212_1564-120 others(16): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 169702777 | |||||
chr4:169702795
|
A | G | 67 | a0001c0001t0033g0279a0001c0001t0042g0268a0001c0001t0045g0280others(64): Show | 69 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.1564-1203A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169702795 | ||||||
chr4:169702831
|
C | G | 65 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0052others(62): Show | 67 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.1564-1167C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169702831 | ||||||
chr4:169702864
|
C | T | 1 | a0001c0002t0002g0092 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1564-1134C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169702864 | ||||||
chr4:169703179
|
T | C | 35 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.1564-819T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169703179 | ||||||
chr4:169703225
|
G | T | 1 | a0001c0001t0001g0114 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1564-773G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169703225 | ||||||
chr4:169703629
|
A | G | 9 | a0001c0001t0006g0197a0001c0001t0006g0198a0001c0001t0006g0199others(6): Show | 9 | HG01884.hp1 HG02572.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.1564-369A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169703629 | ||||||
chr4:169703664
|
C | CT | 48 | a0001c0001t0025g0002a0001c0003t0003g0001a0001c0003t0003g0003others(45): Show | 51 | HG00639.hp2 HG01175.hp2 HG01346.hp1 others(48): Show |
intron_variant | MODIFIER | c.1564-324dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 169703664 | |||||
chr4:169703947
|
G | A | 1 | a0001c0001t0006g0197 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1564-51G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169703947 | ||||||
chr4:169704241
|
G | A | 1 | a0001c0001t0043g0260 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1750+57G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 10/12 | chr4 | 169704241 | ||||||
chr4:169704298
|
G | A | 1 | a0001c0001t0044g0232 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1750+114G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 10/12 | chr4 | 169704298 | ||||||
chr4:169704325
|
G | A | 1 | a0001c0002t0002g0101 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1750+141G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 10/12 | chr4 | 169704325 | ||||||
chr4:169704483
|
C | G | 1 | a0001c0001t0010g0238 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1750+299C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 10/12 | chr4 | 169704483 | ||||||
chr4:169704492
|
C | G | 1 | a0001c0002t0051g0031 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1750+308C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 10/12 | chr4 | 169704492 | ||||||
chr4:169705149
|
G | T | 6 | a0001c0003t0003g0001a0001c0003t0003g0269a0001c0003t0003g0271others(3): Show | 7 | HG02280.hp1 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1750+965G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 10/12 | chr4 | 169705149 | ||||||
chr4:169705240
|
C | T | 24 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(21): Show | 26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.1750+1056C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 10/12 | chr4 | 169705240 | ||||||
chr4:169705269
|
A | G | 1 | a0001c0001t0042g0268 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1750+1085A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 10/12 | chr4 | 169705269 | ||||||
chr4:169705401
|
T | C | 95 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(92): Show | 97 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.1750+1217T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 10/12 | chr4 | 169705401 | ||||||
chr4:169705690
|
T | C | 8 | a0001c0003t0004g0044a0001c0003t0004g0045a0001c0003t0004g0046others(5): Show | 8 | HG00639.hp2 HG01884.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1751-1178T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 10/12 | chr4 | 169705690 | ||||||
chr4:169705747
|
C | T | 66 | a0001c0001t0042g0268a0001c0002t0002g0004a0001c0002t0002g0032others(63): Show | 68 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.1751-1121C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 10/12 | chr4 | 169705747 | ||||||
chr4:169705776
|
C | T | 6 | a0001c0001t0006g0197a0001c0001t0006g0199a0001c0001t0006g0200others(3): Show | 6 | HG01884.hp1 HG02572.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1751-1092C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 10/12 | chr4 | 169705776 | ||||||
chr4:169705894
|
G | A | 9 | a0001c0001t0007g0214a0001c0001t0007g0217a0001c0001t0011g0191others(6): Show | 9 | HG00323.hp2 HG00733.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1751-974G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 10/12 | chr4 | 169705894 | ||||||
chr4:169705968
|
C | G | 6 | a0001c0001t0013g0233a0001c0001t0013g0237a0001c0001t0013g0261others(3): Show | 6 | HG01099.hp1 HG01433.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.1751-900C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 10/12 | chr4 | 169705968 | ||||||
chr4:169706071
|
G | A | 1 | a0001c0003t0023g0035 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1751-797G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 10/12 | chr4 | 169706071 | ||||||
chr4:169706132
|
G | A | 2 | a0001c0001t0001g0148a0001c0001t0001g0159 | 2 | HG02027.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1751-736G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 10/12 | chr4 | 169706132 | ||||||
chr4:169706181
|
A | G | 1 | a0001c0001t0034g0241 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1751-687A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 10/12 | chr4 | 169706181 | ||||||
chr4:169706293
|
C | T | 1 | a0001c0001t0035g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1751-575C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 10/12 | chr4 | 169706293 | ||||||
chr4:169706464
|
TTTG | T | 3 | a0001c0001t0001g0149a0001c0001t0001g0153a0001c0001t0001g0167 | 3 | HG00558.hp2 HG02040.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1751-402_1751-400d others(5): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 169706464 | |||||
chr4:169706624
|
G | C | 4 | a0001c0003t0003g0016a0001c0003t0003g0017a0001c0003t0003g0018others(1): Show | 4 | HG02055.hp2 HG02886.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1751-244G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 10/12 | chr4 | 169706624 | ||||||
chr4:169706760
|
C | T | 1 | a0001c0003t0003g0272 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1751-108C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 10/12 | chr4 | 169706760 | ||||||
chr4:169707323
|
A | G | 96 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(93): Show | 98 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.2149+57A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169707323 | ||||||
chr4:169707373
|
A | G | 150 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(147): Show | 154 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.2149+107A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169707373 | ||||||
chr4:169707463
|
A | G | 1 | a0001c0001t0034g0241 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2149+197A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169707463 | ||||||
chr4:169707600
|
G | T | 2 | a0001c0003t0022g0207a0001c0003t0022g0208 | 2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2149+334G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169707600 | ||||||
chr4:169707883
|
A | G | 1 | a0001c0001t0001g0168 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2149+617A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169707883 | ||||||
chr4:169708583
|
C | T | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2149+1317C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169708583 | ||||||
chr4:169709095
|
T | G | 1 | a0001c0001t0052g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2149+1829T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169709095 | ||||||
chr4:169709308
|
C | T | 1 | a0001c0001t0042g0268 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2149+2042C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169709308 | ||||||
chr4:169709331
|
T | C | 280 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(277): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.2149+2065T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169709331 | ||||||
chr4:169709382
|
T | TA | 29 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(26): Show | 31 | HG01175.hp2 HG01346.hp1 HG01516.hp2 others(28): Show |
intron_variant | MODIFIER | c.2149+2129dupA | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 169709382 | |||||
chr4:169709554
|
G | A | 25 | a0001c0001t0034g0241a0001c0003t0003g0001a0001c0003t0003g0003others(22): Show | 27 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(24): Show |
intron_variant | MODIFIER | c.2149+2288G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169709554 | ||||||
chr4:169709589
|
G | A | 2 | a0001c0001t0033g0279a0001c0001t0045g0280 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2149+2323G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169709589 | ||||||
chr4:169709644
|
A | T | 34 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(31): Show | 34 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.2149+2378A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169709644 | ||||||
chr4:169709677
|
C | CA | 28 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0010g0236others(25): Show | 30 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.2149+2424dupA | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 169709677 | |||||
chr4:169709949
|
TTGTC | T | 34 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(31): Show | 34 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.2149+2686_2149+268 others(8): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 169709949 | |||||
chr4:169709995
|
G | A | 35 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.2149+2729G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169709995 | ||||||
chr4:169710201
|
G | T | 1 | a0001c0001t0001g0266 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2150-2878G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169710201 | ||||||
chr4:169710559
|
C | T | 2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | HG02109.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2150-2520C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169710559 | ||||||
chr4:169710690
|
T | G | 1 | a0001c0001t0042g0268 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2150-2389T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169710690 | ||||||
chr4:169710765
|
A | G | 4 | a0001c0002t0008g0204a0001c0002t0008g0205a0001c0002t0008g0206others(1): Show | 4 | HG02809.hp2 HG02965.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.2150-2314A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169710765 | ||||||
chr4:169710777
|
A | T | 4 | a0001c0003t0003g0021a0001c0003t0003g0025a0001c0003t0003g0026others(1): Show | 4 | HG01981.hp1 NA18989.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.2150-2302A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169710777 | ||||||
chr4:169710879
|
G | C | 1 | a0001c0001t0013g0233 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2150-2200G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169710879 | ||||||
chr4:169710968
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2150-2111A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169710968 | ||||||
chr4:169711105
|
T | C | 2 | a0001c0001t0010g0209a0001c0001t0016g0211 | 2 | HG02602.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.2150-1974T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169711105 | ||||||
chr4:169711155
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2150-1924G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169711155 | ||||||
chr4:169711331
|
A | G | 66 | a0001c0001t0042g0268a0001c0002t0002g0004a0001c0002t0002g0032others(63): Show | 68 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.2150-1748A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169711331 | ||||||
chr4:169711512
|
A | G | 266 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(263): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.2150-1567A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169711512 | ||||||
chr4:169711570
|
G | A | 1 | a0001c0007t0001g0162 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2150-1509G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169711570 | ||||||
chr4:169711869
|
T | A | 61 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(58): Show | 63 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.2150-1210T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169711869 | ||||||
chr4:169711884
|
C | T | 35 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.2150-1195C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169711884 | ||||||
chr4:169711900
|
T | G | 4 | a0001c0003t0003g0021a0001c0003t0003g0025a0001c0003t0003g0026others(1): Show | 4 | HG01981.hp1 NA18989.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.2150-1179T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169711900 | ||||||
chr4:169711958
|
G | A | 1 | a0001c0002t0002g0089 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2150-1121G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169711958 | ||||||
chr4:169712021
|
A | AT | 24 | a0001c0001t0001g0116a0001c0001t0001g0120a0001c0001t0001g0125others(21): Show | 24 | HG01106.hp1 HG01106.hp2 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.2150-1036dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 169712021 | |||||
chr4:169712021
|
A | ATT | 25 | a0001c0001t0001g0161a0001c0001t0042g0268a0001c0002t0002g0064others(22): Show | 27 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(24): Show |
intron_variant | MODIFIER | c.2150-1037_2150-103 others(6): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 169712021 | |||||
chr4:169712021
|
AT | A | 7 | a0001c0001t0001g0113a0001c0001t0001g0128a0001c0001t0001g0131others(4): Show | 7 | HG02451.hp2 HG02572.hp1 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.2150-1036delT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 169712021 | |||||
chr4:169712021
|
ATTTTTTT | A | 34 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(31): Show | 34 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.2150-1042_2150-103 others(11): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 169712021 | |||||
chr4:169712071
|
A | C | 152 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(149): Show | 157 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.2150-1008A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169712071 | ||||||
chr4:169712300
|
C | A | 25 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(22): Show | 27 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(24): Show |
intron_variant | MODIFIER | c.2150-779C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169712300 | ||||||
chr4:169712574
|
A | G | 2 | a0001c0001t0001g0125a0001c0001t0019g0124 | 2 | HG01496.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2150-505A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169712574 | ||||||
chr4:169712730
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2150-349C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169712730 | ||||||
chr4:169712760
|
C | G | 1 | a0001c0003t0037g0040 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2150-319C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169712760 | ||||||
chr4:169713400
|
G | A | 10 | a0001c0003t0004g0034a0001c0003t0004g0036a0001c0003t0004g0037others(7): Show | 10 | HG01175.hp2 HG01358.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.2366+105G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169713400 | ||||||
chr4:169713503
|
C | T | 2 | a0001c0001t0033g0279a0001c0001t0045g0280 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2366+208C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169713503 | ||||||
chr4:169713552
|
G | T | 1 | a0001c0001t0034g0241 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2366+257G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169713552 | ||||||
chr4:169713875
|
T | G | 1 | a0001c0001t0025g0002 | 2 | HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2366+580T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169713875 | ||||||
chr4:169713953
|
A | G | 65 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0052others(62): Show | 67 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.2366+658A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169713953 | ||||||
chr4:169714046
|
A | G | 20 | a0001c0001t0025g0002a0001c0001t0052g0030a0001c0003t0004g0034others(17): Show | 21 | HG00639.hp2 HG01175.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.2366+751A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169714046 | ||||||
chr4:169714167
|
C | T | 2 | a0001c0001t0007g0214a0001c0001t0007g0217 | 2 | HG00323.hp2 HG00733.hp2 |
intron_variant | MODIFIER | c.2366+872C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169714167 | ||||||
chr4:169714238
|
G | A | 3 | a0001c0003t0003g0013a0001c0003t0003g0023a0001c0003t0003g0024 | 3 | NA18982.hp1 NA18984.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.2366+943G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169714238 | ||||||
chr4:169714261
|
CAG | C | 4 | a0001c0002t0008g0204a0001c0002t0008g0205a0001c0002t0008g0206others(1): Show | 4 | HG02809.hp2 HG02965.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.2366+970_2366+971d others(4): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 169714261 | |||||
chr4:169714286
|
G | GT | 59 | a0001c0001t0006g0197a0001c0001t0012g0259a0001c0001t0012g0262others(56): Show | 61 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.2366+1003dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 169714286 | |||||
chr4:169714339
|
T | C | 1 | a0001c0001t0001g0011 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2366+1044T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169714339 | ||||||
chr4:169714430
|
C | G | 1 | a0001c0003t0003g0027 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2366+1135C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169714430 | ||||||
chr4:169714439
|
G | A | 25 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(22): Show | 27 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(24): Show |
intron_variant | MODIFIER | c.2366+1144G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169714439 | ||||||
chr4:169714452
|
G | T | 281 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(278): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.2366+1157G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169714452 | ||||||
chr4:169714453
|
C | A | 93 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(90): Show | 94 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.2366+1158C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169714453 | ||||||
chr4:169714485
|
A | G | 35 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.2366+1190A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169714485 | ||||||
chr4:169714730
|
C | T | 23 | a0001c0003t0004g0033a0001c0003t0004g0034a0001c0003t0004g0036others(20): Show | 23 | HG00639.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.2366+1435C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169714730 | ||||||
chr4:169714906
|
T | C | 2 | a0001c0001t0005g0254a0001c0001t0005g0255 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2366+1611T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169714906 | ||||||
chr4:169715312
|
C | T | 3 | a0001c0002t0002g0055a0001c0002t0002g0063a0001c0002t0002g0064 | 3 | HG01978.hp1 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2366+2017C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169715312 | ||||||
chr4:169715414
|
A | G | 23 | a0001c0003t0004g0033a0001c0003t0004g0034a0001c0003t0004g0036others(20): Show | 23 | HG00639.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.2366+2119A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169715414 | ||||||
chr4:169715494
|
G | A | 1 | a0001c0001t0035g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2366+2199G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169715494 | ||||||
chr4:169715748
|
T | C | 24 | a0001c0001t0025g0002a0001c0003t0004g0033a0001c0003t0004g0034others(21): Show | 25 | HG00639.hp2 HG01175.hp2 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.2366+2453T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169715748 | ||||||
chr4:169715821
|
G | GA | 266 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(263): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.2366+2532dupA | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 169715821 | |||||
chr4:169715902
|
G | C | 1 | a0001c0001t0042g0268 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2366+2607G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169715902 | ||||||
chr4:169716119
|
C | G | 2 | a0001c0003t0020g0183a0001c0003t0020g0184 | 2 | HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2366+2824C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169716119 | ||||||
chr4:169716367
|
C | T | 25 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0013others(22): Show | 27 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(24): Show |
intron_variant | MODIFIER | c.2366+3072C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169716367 | ||||||
chr4:169716421
|
C | G | 1 | a0001c0002t0008g0204 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2366+3126C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169716421 | ||||||
chr4:169716515
|
T | TA | 23 | a0001c0003t0004g0033a0001c0003t0004g0034a0001c0003t0004g0036others(20): Show | 23 | HG00639.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.2366+3228dupA | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 169716515 | |||||
chr4:169716959
|
T | A | 5 | a0001c0002t0009g0053a0001c0002t0009g0096a0001c0002t0009g0097others(2): Show | 5 | HG02109.hp2 HG02451.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.2367-2948T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169716959 | ||||||
chr4:169717101
|
A | G | 1 | a0001c0001t0006g0198 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2367-2806A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169717101 | ||||||
chr4:169717197
|
C | G | 1 | a0001c0001t0001g0165 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2367-2710C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169717197 | ||||||
chr4:169717265
|
A | G | 5 | a0001c0001t0001g0141a0001c0001t0001g0144a0001c0001t0001g0145others(2): Show | 5 | HG01192.hp1 HG03491.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.2367-2642A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169717265 | ||||||
chr4:169717315
|
C | T | 83 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(80): Show | 84 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.2367-2592C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169717315 | ||||||
chr4:169717390
|
G | T | 2 | a0001c0003t0020g0183a0001c0003t0020g0184 | 2 | HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2367-2517G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169717390 | ||||||
chr4:169717740
|
ACT | A | 66 | a0001c0001t0042g0268a0001c0002t0002g0004a0001c0002t0002g0032others(63): Show | 68 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.2367-2164_2367-216 others(6): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 169717740 | |||||
chr4:169717741
|
C | G | 6 | a0001c0001t0005g0246a0001c0001t0005g0247a0001c0001t0005g0249others(3): Show | 6 | HG01109.hp1 HG02258.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.2367-2166C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169717741 | ||||||
chr4:169717983
|
A | G | 1 | a0001c0001t0030g0245 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2367-1924A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169717983 | ||||||
chr4:169718267
|
T | C | 2 | a0001c0003t0022g0207a0001c0003t0022g0208 | 2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2367-1640T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169718267 | ||||||
chr4:169718299
|
T | C | 65 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0052others(62): Show | 67 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.2367-1608T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169718299 | ||||||
chr4:169718470
|
T | A | 1 | a0001c0003t0003g0022 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2367-1437T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169718470 | ||||||
chr4:169718825
|
G | A | 2 | a0001c0003t0020g0183a0001c0003t0020g0184 | 2 | HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2367-1082G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169718825 | ||||||
chr4:169718906
|
A | G | 1 | a0001c0003t0004g0039 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2367-1001A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169718906 | ||||||
chr4:169718941
|
A | C | 1 | a0001c0002t0002g0101 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2367-966A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169718941 | ||||||
chr4:169719003
|
A | T | 89 | a0001c0001t0042g0268a0001c0002t0002g0004a0001c0002t0002g0032others(86): Show | 91 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.2367-904A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169719003 | ||||||
chr4:169719094
|
G | A | 1 | a0001c0001t0013g0233 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2367-813G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169719094 | ||||||
chr4:169719256
|
G | A | 1 | a0001c0001t0052g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2367-651G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169719256 | ||||||
chr4:169719270
|
T | G | 151 | a0001c0001t0007g0103a0001c0001t0007g0212a0001c0001t0007g0213others(148): Show | 155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.2367-637T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169719270 | ||||||
chr4:169719395
|
C | T | 1 | a0001c0006t0046g0220 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2367-512C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169719395 | ||||||
chr4:169719567
|
A | G | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG02257.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2367-340A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169719567 | ||||||
chr4:169719640
|
A | C | 24 | a0001c0001t0025g0002a0001c0003t0004g0033a0001c0003t0004g0034others(21): Show | 25 | HG00639.hp2 HG01175.hp2 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.2367-267A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169719640 | ||||||
chr4:169719668
|
G | C | 1 | a0001c0001t0001g0181 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2367-239G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169719668 | ||||||
chr4:169719842
|
T | C | 90 | a0001c0001t0025g0002a0001c0001t0042g0268a0001c0002t0002g0004others(87): Show | 93 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.2367-65T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169719842 | ||||||
chr4:169719899
|
C | T | 2 | a0001c0003t0022g0207a0001c0003t0022g0208 | 2 | HG02723.hp2 HG03041.hp2 |
splice_region_variant&intron_variant | LOW | c.2367-8C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169719899 |