geneid | 29099 |
---|---|
ensemblid | ENSG00000110442.12 |
hgncid | 25014 |
symbol | COMMD9 |
name | COMM domain containing 9 |
refseq_nuc | NM_014186.4 |
refseq_prot | NP_054905.2 |
ensembl_nuc | ENST00000263401.10 |
ensembl_prot | ENSP00000263401.5 |
mane_status | MANE Select |
chr | chr11 |
start | 36272292 |
end | 36289424 |
strand | - |
ver | v1.2 |
region | chr11:36272292-36289424 |
region5000 | chr11:36267292-36294424 |
regionname0 | COMMD9_chr11_36272292_36289424 |
regionname5000 | COMMD9_chr11_36267292_36294424 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 198 | 443 | 92 | 79 | 212 | 16 | 42 | 166 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
a0002 | 0/0 | 198 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
a0003 | 0/0 | 198 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 597 | 440 | 91 | 79 | 212 | 15 | 41 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
c0002 | 0/0 | 597 | 3 | 3 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
c0003 | 0/0 | 597 | 2 | 1 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
c0004 | 0/0 | 597 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
c0005 | 0/0 | 597 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
c0006 | 0/0 | 597 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 2353 | 233 | 40 | 51 | 100 | 11 | 30 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
t0002 | 0/0 | 2353 | 89 | 21 | 6 | 55 | 2 | 5 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
t0003 | 0/0 | 2353 | 47 | 9 | 7 | 31 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
t0004 | 0/0 | 2347 | 34 | 0 | 12 | 21 | 1 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
t0005 | 0/0 | 2353 | 17 | 5 | 2 | 2 | 2 | 6 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
t0006 | 0/0 | 2353 | 8 | 8 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
t0007 | 0/0 | 2353 | 5 | 5 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
t0008 | 0/0 | 2353 | 3 | 0 | 0 | 3 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
t0009 | 1/0 | 2353 | 3 | 2 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
t0010 | 0/0 | 2353 | 2 | 2 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
t0011 | 0/0 | 2353 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
t0012 | 0/0 | 2353 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
t0013 | 0/0 | 2343 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
t0014 | 0/0 | 2353 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
t0015 | 0/0 | 2353 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
t0016 | 0/0 | 2353 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
t0017 | 0/0 | 2353 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 14 | 0 | 3 | 11 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0002 | 0/0 | 7 | 0 | 0 | 5 | 2 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0003 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0007 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0008 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0009 | 0/0 | 5 | 0 | 2 | 2 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0010 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0011 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0012 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0013 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0015 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0017 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0023 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0036 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0037 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0038 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0042 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0045 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0047 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0050 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0054 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0055 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0056 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0059 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0060 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0061 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0062 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0063 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0064 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0065 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0170 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 597 | 440 | 91 | 79 | 212 | 15 | 41 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
a0001c0004 | 0/0 | 597 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
a0001c0005 | 0/0 | 597 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
a0001c0006 | 0/0 | 597 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
a0002c0002 | 0/0 | 597 | 3 | 3 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
a0003c0003 | 0/0 | 597 | 2 | 1 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2949 | 231 | 40 | 51 | 100 | 10 | 29 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
a0001c0001t0002 | 0/0 | 2949 | 89 | 21 | 6 | 55 | 2 | 5 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
a0001c0001t0003 | 0/0 | 2949 | 47 | 9 | 7 | 31 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
a0001c0001t0004 | 0/0 | 2943 | 34 | 0 | 12 | 21 | 1 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
a0001c0001t0005 | 0/0 | 2949 | 15 | 4 | 1 | 2 | 2 | 6 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
a0001c0001t0006 | 0/0 | 2949 | 5 | 5 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
a0001c0001t0007 | 0/0 | 2949 | 4 | 4 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
a0001c0001t0008 | 0/0 | 2949 | 3 | 0 | 0 | 3 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
a0001c0001t0009 | 1/0 | 2949 | 3 | 2 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
a0001c0001t0010 | 0/0 | 2949 | 2 | 2 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
a0001c0001t0011 | 0/0 | 2949 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
a0001c0001t0012 | 0/0 | 2949 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
a0001c0001t0013 | 0/0 | 2939 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
a0001c0001t0014 | 0/0 | 2949 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
a0001c0001t0015 | 0/0 | 2949 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
a0001c0001t0016 | 0/0 | 2949 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
a0001c0001t0017 | 0/0 | 2949 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
a0001c0004t0007 | 0/0 | 2949 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
a0001c0005t0001 | 0/0 | 2949 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
a0001c0006t0001 | 0/0 | 2949 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
a0002c0002t0006 | 0/0 | 2949 | 3 | 3 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
a0003c0003t0005 | 0/0 | 2949 | 2 | 1 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | copy fasta | chr11 | 36267292 | 36294424 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 7 | 0 | 0 | 5 | 2 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0003 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0007 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0009 | 0/0 | 5 | 0 | 2 | 2 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0012 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0013 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0047 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0050 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0054 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0055 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0056 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0059 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0060 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0061 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0062 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0063 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0065 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0170 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0003g0001 | 0/0 | 14 | 0 | 3 | 11 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0003g0008 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0003g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0003g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0003g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0003g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0003g0045 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0003g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0004g0011 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0004g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0004g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0004g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0004g0042 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0004g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0004g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0004g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0005g0036 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0005g0064 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0005g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0005g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0005g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0005g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0005g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0005g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0005g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0005g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0005g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0005g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0005g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0006g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0006g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0006g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0006g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0006g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0007g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0007g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0007g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0008g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0008g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0008g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0009g0015 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0010g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0010g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0011g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0012g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0013g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0014g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0015g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0016g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0001t0017g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0004t0007g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0005t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0001c0006t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0002c0002t0006g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0002c0002t0006g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0002c0002t0006g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0003c0003t0005g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
a0003c0003t0005g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0004 | g0011 | EUR | GBR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG00099 | hp2 | a0001 | c0006 | t0001 | g0177 | EUR | GBR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0125 | EUR | FIN | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0293 | EUR | FIN | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0189 | EUR | FIN | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0309 | EUR | FIN | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | CHS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | CHS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | CHS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | CHS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG00438 | hp2 | a0001 | c0001 | t0005 | g0064 | EAS | CHS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG00558 | hp2 | a0001 | c0001 | t0004 | g0199 | EAS | CHS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG00597 | hp1 | a0001 | c0001 | t0008 | g0093 | EAS | CHS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | CHS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | CHS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG00621 | hp1 | a0001 | c0001 | t0004 | g0197 | EAS | CHS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | CHS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG00639 | hp1 | a0001 | c0001 | t0004 | g0011 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0311 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG00642 | hp2 | a0001 | c0001 | t0004 | g0020 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG00673 | hp1 | a0001 | c0001 | t0004 | g0302 | EAS | CHS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | CHS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG00733 | hp2 | a0001 | c0001 | t0005 | g0150 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG00735 | hp1 | a0001 | c0001 | t0004 | g0312 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0270 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01071 | hp2 | a0001 | c0001 | t0004 | g0020 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01106 | hp2 | a0001 | c0001 | t0004 | g0020 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01109 | hp1 | a0003 | c0003 | t0005 | g0066 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0045 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01175 | hp2 | a0001 | c0001 | t0004 | g0011 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0106 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0223 | AMR | PUR | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | CLM | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | CLM | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01261 | hp2 | a0001 | c0001 | t0004 | g0011 | AMR | CLM | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | CLM | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | CLM | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | CLM | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | IBS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0059 | EUR | IBS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0068 | EUR | IBS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0023 | EUR | IBS | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | ACB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | ACB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0081 | AFR | ACB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0310 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01934 | hp2 | a0001 | c0001 | t0004 | g0209 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01975 | hp1 | a0001 | c0001 | t0015 | g0262 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01981 | hp2 | a0001 | c0001 | t0004 | g0042 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | KHV | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | KHV | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | KHV | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | KHV | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | ACB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | KHV | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | KHV | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | KHV | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02080 | hp1 | a0001 | c0001 | t0004 | g0195 | EAS | KHV | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02080 | hp2 | a0001 | c0001 | t0004 | g0042 | EAS | KHV | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | KHV | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | KHV | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | KHV | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | KHV | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | ACB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02145 | hp2 | a0001 | c0001 | t0013 | g0187 | AFR | ACB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02148 | hp2 | a0001 | c0001 | t0004 | g0021 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CDX | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | CDX | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CDX | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0082 | AFR | ACB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02273 | hp1 | a0001 | c0001 | t0004 | g0021 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0222 | AFR | ACB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02293 | hp1 | a0001 | c0001 | t0004 | g0021 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0215 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02451 | hp1 | a0001 | c0001 | t0007 | g0184 | AFR | ACB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | ACB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0221 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02602 | hp2 | a0001 | c0001 | t0017 | g0317 | SAS | PJL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02615 | hp1 | a0002 | c0002 | t0006 | g0078 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02615 | hp2 | a0003 | c0003 | t0005 | g0067 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02622 | hp2 | a0001 | c0001 | t0005 | g0146 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0099 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02723 | hp1 | a0001 | c0001 | t0009 | g0015 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02735 | hp1 | a0001 | c0001 | t0005 | g0140 | SAS | PJL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0072 | SAS | PJL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0097 | SAS | PJL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02738 | hp2 | a0001 | c0001 | t0005 | g0143 | SAS | PJL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02809 | hp2 | a0001 | c0001 | t0012 | g0144 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0087 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02886 | hp2 | a0001 | c0001 | t0016 | g0245 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02895 | hp2 | a0001 | c0001 | t0007 | g0193 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0083 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | ESN | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ESN | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | ESN | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02965 | hp2 | a0001 | c0004 | t0007 | g0194 | AFR | ESN | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02970 | hp1 | a0001 | c0001 | t0010 | g0291 | AFR | ESN | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0130 | AFR | ESN | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02976 | hp2 | a0001 | c0001 | t0006 | g0137 | AFR | ESN | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0080 | SAS | PJL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03041 | hp1 | a0001 | c0001 | t0005 | g0151 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03041 | hp2 | a0001 | c0001 | t0011 | g0153 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03098 | hp1 | a0001 | c0001 | t0009 | g0015 | AFR | MSL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | MSL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0214 | AFR | ESN | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | ESN | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0046 | AFR | ESN | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ESN | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | MSL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03209 | hp2 | a0001 | c0001 | t0005 | g0149 | AFR | MSL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | MSL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03225 | hp2 | a0001 | c0001 | t0010 | g0287 | AFR | MSL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03453 | hp1 | a0001 | c0001 | t0007 | g0040 | AFR | MSL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03453 | hp2 | a0001 | c0001 | t0006 | g0138 | AFR | MSL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | ESN | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03516 | hp2 | a0002 | c0002 | t0006 | g0079 | AFR | ESN | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | GWD | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0212 | AFR | MSL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0295 | SAS | PJL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | STU | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03688 | hp2 | a0001 | c0001 | t0005 | g0142 | SAS | STU | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03710 | hp2 | a0001 | c0001 | t0005 | g0036 | SAS | PJL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | BEB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | BEB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | BEB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | BEB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | BEB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0109 | SAS | BEB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03942 | hp1 | a0001 | c0001 | t0005 | g0147 | SAS | BEB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03942 | hp2 | a0001 | c0005 | t0001 | g0230 | SAS | BEB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | STU | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | STU | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | BEB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0089 | SAS | BEB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | STU | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0294 | SAS | STU | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | STU | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG04204 | hp2 | a0001 | c0001 | t0005 | g0145 | SAS | STU | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | STU | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | STU | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18522 | hp1 | a0001 | c0001 | t0007 | g0040 | AFR | YRI | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18522 | hp2 | a0001 | c0001 | t0005 | g0148 | AFR | YRI | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | CHB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | CHB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | CHB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18906 | hp1 | a0002 | c0002 | t0006 | g0077 | AFR | YRI | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | YRI | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18939 | hp2 | a0001 | c0001 | t0008 | g0074 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0318 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18945 | hp2 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18952 | hp1 | a0001 | c0001 | t0004 | g0211 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18953 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18967 | hp1 | a0001 | c0001 | t0004 | g0210 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18967 | hp2 | a0001 | c0001 | t0008 | g0094 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18972 | hp1 | a0001 | c0001 | t0004 | g0198 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18972 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18973 | hp2 | a0001 | c0001 | t0004 | g0201 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18974 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18978 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18980 | hp1 | a0001 | c0001 | t0004 | g0202 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18991 | hp2 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18995 | hp1 | a0001 | c0001 | t0004 | g0200 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19000 | hp2 | a0001 | c0001 | t0004 | g0261 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19001 | hp2 | a0001 | c0001 | t0005 | g0064 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19004 | hp2 | a0001 | c0001 | t0004 | g0205 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19006 | hp1 | a0001 | c0001 | t0004 | g0208 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19009 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | LWK | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | LWK | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | LWK | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0086 | AFR | LWK | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19054 | hp2 | a0001 | c0001 | t0004 | g0203 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19056 | hp1 | a0001 | c0001 | t0004 | g0206 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19056 | hp2 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19064 | hp1 | a0001 | c0001 | t0004 | g0204 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19077 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19083 | hp2 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19085 | hp1 | a0001 | c0001 | t0004 | g0207 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0319 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19091 | hp2 | a0001 | c0001 | t0004 | g0196 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | YRI | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0046 | AFR | YRI | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ASW | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | ASW | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0102 | EUR | TSI | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA20752 | hp2 | a0001 | c0001 | t0005 | g0141 | EUR | TSI | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0282 | EUR | TSI | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA20805 | hp2 | a0001 | c0001 | t0005 | g0036 | EUR | TSI | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | GIH | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | GIH | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01123 | hp1 | a0001 | c0001 | t0014 | g0185 | AMR | CLM | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02109 | hp1 | a0001 | c0001 | t0006 | g0131 | AFR | ACB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0127 | AFR | ACB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | ACB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | ACB | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | MSL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG03471 | hp2 | a0001 | c0001 | t0006 | g0136 | AFR | MSL | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | USA | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | USA | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | USA | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA20300 | hp2 | a0001 | c0001 | t0006 | g0135 | AFR | USA | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | LWK | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0170 | REF | REF | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0009 | g0015 | REF | REF | COMMD9_chr11_36267292_36294424 | COMMD9 | chr11 | 36267292 | 36294424 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:36276183
|
T | A | 1 | a0003 | 2 | HG01109.hp1 HG02615.hp2 |
missense_variant | MODERATE | c.410A>T | p.Asp137Val | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 5/6 | 422/2949 | 410/597 | 137/198 | chr11 | 36276183 | ||
chr11:36277107
|
C | T | 1 | a0002 | 3 | HG02615.hp1 HG03516.hp2 NA18906.hp1 |
missense_variant | MODERATE | c.334G>A | p.Glu112Lys | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 4/6 | 346/2949 | 334/597 | 112/198 | chr11 | 36277107 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:36274647
|
G | A | 1 | a0001c0004 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.582C>T | p.Ala194Ala | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 6/6 | 594/2949 | 582/597 | 194/198 | chr11 | 36274647 | ||
chr11:36276161
|
G | A | 1 | a0001c0005 | 1 | HG03942.hp2 | synonymous_variant | LOW | c.432C>T | p.Val144Val | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 5/6 | 444/2949 | 432/597 | 144/198 | chr11 | 36276161 | ||
chr11:36278557
|
G | A | 1 | a0001c0006 | 1 | HG00099.hp2 | synonymous_variant | LOW | c.237C>T | p.Ala79Ala | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 3/6 | 249/2949 | 237/597 | 79/198 | chr11 | 36278557 | ||
chr11:36289362
|
C | T | 1 | a0003c0003 | 2 | HG01109.hp1 HG02615.hp2 |
splice_region_variant&synonymous_variant | LOW | c.51G>A | p.Lys17Lys | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/6 | 63/2949 | 51/597 | 17/198 | chr11 | 36289362 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:36272484
|
C | G | 7 | a0001c0001t0002a0001c0001t0005a0001c0001t0007others(4): Show | 115 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*2148G>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 6/6 | 2148 | chr11 | 36272484 | |||||
chr11:36272502
|
A | G | 4 | a0001c0001t0002a0001c0001t0007a0001c0001t0008others(1): Show | 97 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*2130T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 6/6 | 2130 | chr11 | 36272502 | |||||
chr11:36272556
|
TGGAGGGT others(3): Show |
T | 1 | a0001c0001t0013 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2066_*2075delCATA others(6): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 6/6 | 2066 | chr11 | 36272556 | |||||
chr11:36272567
|
A | T | 1 | a0001c0001t0013 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2065T>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 6/6 | 2065 | chr11 | 36272567 | |||||
chr11:36272572
|
G | C | 1 | a0001c0001t0014 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2060C>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 6/6 | 2060 | chr11 | 36272572 | |||||
chr11:36272689
|
T | G | 2 | a0001c0001t0007a0001c0004t0007 | 5 | HG02451.hp1 HG02895.hp2 HG02965.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1943A>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 6/6 | 1943 | chr11 | 36272689 | |||||
chr11:36272830
|
G | A | 3 | a0001c0001t0005a0001c0001t0012a0003c0003t0005 | 18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1802C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 6/6 | 1802 | chr11 | 36272830 | |||||
chr11:36273368
|
C | T | 1 | a0001c0001t0003 | 47 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1264G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 6/6 | 1264 | chr11 | 36273368 | |||||
chr11:36273378
|
G | A | 2 | a0001c0001t0005a0003c0003t0005 | 17 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1254C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 6/6 | 1254 | chr11 | 36273378 | |||||
chr11:36273404
|
A | T | 3 | a0001c0001t0005a0001c0001t0012a0003c0003t0005 | 18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1228T>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 6/6 | 1228 | chr11 | 36273404 | |||||
chr11:36273484
|
ATTTATT | A | 1 | a0001c0001t0004 | 34 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1142_*1147delAATA others(2): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 6/6 | 1142 | chr11 | 36273484 | |||||
chr11:36273534
|
T | G | 1 | a0001c0001t0015 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1098A>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 6/6 | 1098 | chr11 | 36273534 | |||||
chr11:36273544
|
C | T | 1 | a0001c0001t0010 | 2 | HG02970.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1088G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 6/6 | 1088 | chr11 | 36273544 | |||||
chr11:36273607
|
G | A | 1 | a0001c0001t0016 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1025C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 6/6 | 1025 | chr11 | 36273607 | |||||
chr11:36273635
|
C | T | 3 | a0001c0001t0005a0001c0001t0012a0003c0003t0005 | 18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*997G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 6/6 | 997 | chr11 | 36273635 | |||||
chr11:36273706
|
T | G | 6 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(3): Show | 105 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*926A>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 6/6 | 926 | chr11 | 36273706 | |||||
chr11:36273773
|
T | C | 1 | a0001c0001t0017 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*859A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 6/6 | 859 | chr11 | 36273773 | |||||
chr11:36273982
|
G | T | 20 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(17): Show | 444 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(441): Show |
3_prime_UTR_variant | MODIFIER | c.*650C>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 6/6 | 650 | chr11 | 36273982 | |||||
chr11:36274361
|
C | T | 1 | a0001c0001t0011 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*271G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 6/6 | 271 | chr11 | 36274361 | |||||
chr11:36274431
|
A | T | 1 | a0001c0001t0008 | 3 | HG00597.hp1 NA18939.hp2 NA18967.hp2 |
3_prime_UTR_variant | MODIFIER | c.*201T>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 6/6 | 201 | chr11 | 36274431 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:36274864
|
C | T | 1 | a0001c0001t0001g0054 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.457-92G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 5/5 | chr11 | 36274864 | ||||||
chr11:36274988
|
A | G | 4 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(1): Show | 4 | HG02717.hp2 HG03130.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.457-216T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 5/5 | chr11 | 36274988 | ||||||
chr11:36275091
|
T | C | 1 | a0001c0001t0017g0317 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.457-319A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 5/5 | chr11 | 36275091 | ||||||
chr11:36275418
|
C | T | 3 | a0001c0001t0001g0314a0001c0001t0001g0315a0001c0001t0001g0316 | 3 | HG01243.hp1 HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.457-646G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 5/5 | chr11 | 36275418 | ||||||
chr11:36275446
|
C | CT | 53 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(50): Show | 85 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.457-675dupA | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 5/5 | chr11 | 36275446 | ||||||
chr11:36275446
|
CT | C | 101 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0012others(98): Show | 138 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.457-675delA | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 5/5 | chr11 | 36275446 | ||||||
chr11:36275470
|
AGTCT | A | 40 | a0001c0001t0001g0019a0001c0001t0001g0047a0001c0001t0001g0048others(37): Show | 49 | HG00323.hp1 HG00609.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.456+663_456+666del others(4): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 5/5 | chr11 | 36275470 | ||||||
chr11:36275476
|
A | G | 3 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0174 | 3 | HG03239.hp1 HG03834.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.456+661T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 5/5 | chr11 | 36275476 | ||||||
chr11:36275513
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.456+624C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 5/5 | chr11 | 36275513 | ||||||
chr11:36275519
|
C | T | 1 | a0001c0001t0015g0262 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.456+618G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 5/5 | chr11 | 36275519 | ||||||
chr11:36275600
|
C | T | 3 | a0001c0001t0001g0314a0001c0001t0001g0315a0001c0001t0001g0316 | 3 | HG01243.hp1 HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.456+537G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 5/5 | chr11 | 36275600 | ||||||
chr11:36275605
|
G | A | 122 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(119): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.456+532C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 5/5 | chr11 | 36275605 | ||||||
chr11:36275632
|
T | C | 40 | a0001c0001t0001g0186a0001c0001t0001g0213a0001c0001t0003g0001others(37): Show | 68 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.456+505A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 5/5 | chr11 | 36275632 | ||||||
chr11:36275635
|
G | T | 1 | a0001c0001t0004g0206 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.456+502C>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 5/5 | chr11 | 36275635 | ||||||
chr11:36275784
|
GCCTAATC others(1): Show |
G | 25 | a0001c0001t0004g0011a0001c0001t0004g0020a0001c0001t0004g0021others(22): Show | 34 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.456+345_456+352del others(8): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 5/5 | chr11 | 36275784 | ||||||
chr11:36275856
|
CACT | C | 3 | a0001c0001t0001g0213a0001c0001t0003g0018a0001c0001t0003g0212 | 5 | HG02559.hp2 HG02965.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.456+278_456+280del others(3): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 5/5 | chr11 | 36275856 | ||||||
chr11:36276480
|
A | C | 3 | a0001c0001t0001g0314a0001c0001t0001g0315a0001c0001t0001g0316 | 3 | HG01243.hp1 HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.353-240T>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 4/5 | chr11 | 36276480 | ||||||
chr11:36276551
|
C | G | 144 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0012others(141): Show | 209 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.353-311G>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 4/5 | chr11 | 36276551 | ||||||
chr11:36276558
|
A | C | 1 | a0001c0001t0001g0176 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.353-318T>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 4/5 | chr11 | 36276558 | ||||||
chr11:36276641
|
T | C | 104 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0012others(101): Show | 141 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.353-401A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 4/5 | chr11 | 36276641 | ||||||
chr11:36276647
|
C | T | 40 | a0001c0001t0001g0019a0001c0001t0001g0047a0001c0001t0001g0048others(37): Show | 49 | HG00323.hp1 HG00609.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.353-407G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 4/5 | chr11 | 36276647 | ||||||
chr11:36276739
|
G | T | 3 | a0001c0001t0001g0213a0001c0001t0003g0018a0001c0001t0003g0212 | 5 | HG02559.hp2 HG02965.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.352+350C>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 4/5 | chr11 | 36276739 | ||||||
chr11:36276814
|
T | A | 1 | a0001c0001t0001g0299 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.352+275A>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 4/5 | chr11 | 36276814 | ||||||
chr11:36276877
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.352+212G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 4/5 | chr11 | 36276877 | ||||||
chr11:36276939
|
A | C | 4 | a0001c0001t0002g0035a0001c0001t0002g0086a0001c0001t0002g0130others(1): Show | 5 | HG01891.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.352+150T>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 4/5 | chr11 | 36276939 | ||||||
chr11:36277005
|
C | T | 213 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 303 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.352+84G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 4/5 | chr11 | 36277005 | ||||||
chr11:36277024
|
G | C | 6 | a0001c0001t0002g0026a0001c0001t0002g0070a0001c0001t0002g0071others(3): Show | 7 | HG01891.hp2 HG02257.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.352+65C>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 4/5 | chr11 | 36277024 | ||||||
chr11:36277052
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.352+37G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 4/5 | chr11 | 36277052 | ||||||
chr11:36277328
|
G | C | 40 | a0001c0001t0001g0186a0001c0001t0001g0213a0001c0001t0003g0001others(37): Show | 68 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.318-205C>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 3/5 | chr11 | 36277328 | ||||||
chr11:36277380
|
C | A | 40 | a0001c0001t0001g0186a0001c0001t0001g0213a0001c0001t0003g0001others(37): Show | 68 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.318-257G>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 3/5 | chr11 | 36277380 | ||||||
chr11:36277414
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.318-291T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 3/5 | chr11 | 36277414 | ||||||
chr11:36277701
|
C | T | 6 | a0001c0001t0001g0048a0001c0001t0001g0051a0001c0001t0001g0239others(3): Show | 8 | HG02257.hp1 HG02572.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.318-578G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 3/5 | chr11 | 36277701 | ||||||
chr11:36277729
|
G | GA | 287 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(284): Show | 388 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(385): Show |
intron_variant | MODIFIER | c.318-607dupT | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 3/5 | chr11 | 36277729 | ||||||
chr11:36277818
|
A | AT | 40 | a0001c0001t0001g0186a0001c0001t0001g0213a0001c0001t0003g0001others(37): Show | 68 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.317+658dupA | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 3/5 | chr11 | 36277818 | ||||||
chr11:36277828
|
T | G | 40 | a0001c0001t0001g0186a0001c0001t0001g0213a0001c0001t0003g0001others(37): Show | 68 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.317+649A>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 3/5 | chr11 | 36277828 | ||||||
chr11:36277878
|
G | A | 25 | a0001c0001t0004g0011a0001c0001t0004g0020a0001c0001t0004g0021others(22): Show | 34 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.317+599C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 3/5 | chr11 | 36277878 | ||||||
chr11:36278024
|
T | C | 3 | a0001c0001t0001g0314a0001c0001t0001g0315a0001c0001t0001g0316 | 3 | HG01243.hp1 HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.317+453A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 3/5 | chr11 | 36278024 | ||||||
chr11:36278098
|
C | A | 1 | a0001c0001t0003g0223 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.317+379G>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 3/5 | chr11 | 36278098 | ||||||
chr11:36278154
|
G | C | 40 | a0001c0001t0001g0186a0001c0001t0001g0213a0001c0001t0003g0001others(37): Show | 68 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.317+323C>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 3/5 | chr11 | 36278154 | ||||||
chr11:36278217
|
C | T | 101 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0012others(98): Show | 138 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.317+260G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 3/5 | chr11 | 36278217 | ||||||
chr11:36278267
|
AG | A | 16 | a0001c0001t0005g0036a0001c0001t0005g0064a0001c0001t0005g0140others(13): Show | 18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.317+209delC | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 3/5 | chr11 | 36278267 | ||||||
chr11:36278426
|
A | T | 46 | a0001c0001t0001g0019a0001c0001t0001g0047a0001c0001t0001g0048others(43): Show | 56 | HG00323.hp1 HG00609.hp2 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.317+51T>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 3/5 | chr11 | 36278426 | ||||||
chr11:36278623
|
G | C | 1 | a0001c0001t0005g0148 | 1 | NA18522.hp2 | splice_region_variant&intron_variant | LOW | c.178-7C>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36278623 | ||||||
chr11:36278629
|
C | T | 1 | a0001c0001t0007g0193 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.178-13G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36278629 | ||||||
chr11:36278661
|
G | A | 16 | a0001c0001t0005g0036a0001c0001t0005g0064a0001c0001t0005g0140others(13): Show | 18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.178-45C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36278661 | ||||||
chr11:36278680
|
G | A | 24 | a0001c0001t0001g0186a0001c0001t0001g0213a0001c0001t0003g0001others(21): Show | 50 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.178-64C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36278680 | ||||||
chr11:36278821
|
G | T | 40 | a0001c0001t0001g0019a0001c0001t0001g0047a0001c0001t0001g0048others(37): Show | 49 | HG00323.hp1 HG00609.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.178-205C>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36278821 | ||||||
chr11:36278834
|
C | G | 314 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(311): Show | 441 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(438): Show |
intron_variant | MODIFIER | c.178-218G>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36278834 | ||||||
chr11:36279016
|
G | C | 314 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(311): Show | 441 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(438): Show |
intron_variant | MODIFIER | c.178-400C>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36279016 | ||||||
chr11:36279031
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0163 | 7 | HG01261.hp1 HG02809.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.178-415C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36279031 | ||||||
chr11:36279052
|
G | T | 16 | a0001c0001t0005g0036a0001c0001t0005g0064a0001c0001t0005g0140others(13): Show | 18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.178-436C>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36279052 | ||||||
chr11:36279074
|
A | G | 1 | a0001c0001t0001g0054 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.178-458T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36279074 | ||||||
chr11:36279124
|
C | T | 16 | a0001c0001t0005g0036a0001c0001t0005g0064a0001c0001t0005g0140others(13): Show | 18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.178-508G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36279124 | ||||||
chr11:36279125
|
G | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0158a0001c0001t0001g0159others(4): Show | 12 | HG01261.hp1 HG02055.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.178-509C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36279125 | ||||||
chr11:36279243
|
G | A | 1 | a0001c0001t0001g0249 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.178-627C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36279243 | ||||||
chr11:36279285
|
C | T | 82 | a0001c0001t0002g0006a0001c0001t0002g0024a0001c0001t0002g0025others(79): Show | 99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.178-669G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36279285 | ||||||
chr11:36279615
|
A | T | 82 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0012others(79): Show | 114 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.178-999T>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36279615 | ||||||
chr11:36279630
|
C | T | 37 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(34): Show | 67 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(64): Show |
intron_variant | MODIFIER | c.178-1014G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36279630 | ||||||
chr11:36279674
|
T | C | 24 | a0001c0001t0001g0186a0001c0001t0001g0213a0001c0001t0003g0001others(21): Show | 50 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.177+1038A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36279674 | ||||||
chr11:36279676
|
G | T | 1 | a0001c0001t0001g0238 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.177+1036C>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36279676 | ||||||
chr11:36279738
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.177+974T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36279738 | ||||||
chr11:36279824
|
G | C | 5 | a0001c0001t0006g0131a0001c0001t0006g0135a0001c0001t0006g0136others(2): Show | 5 | HG02109.hp1 HG02976.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.177+888C>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36279824 | ||||||
chr11:36280006
|
T | A | 82 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0012others(79): Show | 114 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.177+706A>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36280006 | ||||||
chr11:36280130
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.177+582A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36280130 | ||||||
chr11:36280133
|
G | A | 1 | a0001c0006t0001g0177 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.177+579C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36280133 | ||||||
chr11:36280298
|
G | A | 22 | a0001c0001t0001g0213a0001c0001t0003g0001a0001c0001t0003g0008others(19): Show | 48 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.177+414C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36280298 | ||||||
chr11:36280503
|
C | T | 1 | a0001c0001t0002g0087 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.177+209G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36280503 | ||||||
chr11:36280643
|
T | C | 1 | a0001c0001t0001g0269 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.177+69A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 2/5 | chr11 | 36280643 | ||||||
chr11:36280860
|
GA | G | 17 | a0001c0001t0004g0302a0001c0001t0005g0036a0001c0001t0005g0064others(14): Show | 19 | HG00438.hp2 HG00673.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.52-24delT | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36280860 | ||||||
chr11:36280971
|
G | A | 1 | a0001c0001t0001g0241 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.52-134C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36280971 | ||||||
chr11:36280978
|
C | G | 1 | a0001c0001t0013g0187 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.52-141G>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36280978 | ||||||
chr11:36281107
|
G | T | 2 | a0001c0001t0001g0294a0001c0001t0001g0295 | 2 | HG03654.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.52-270C>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36281107 | ||||||
chr11:36281239
|
T | C | 17 | a0001c0001t0001g0152a0001c0001t0005g0036a0001c0001t0005g0064others(14): Show | 19 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.52-402A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36281239 | ||||||
chr11:36281316
|
A | G | 24 | a0001c0001t0001g0186a0001c0001t0001g0213a0001c0001t0003g0001others(21): Show | 50 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.52-479T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36281316 | ||||||
chr11:36281550
|
T | G | 7 | a0001c0001t0002g0030a0001c0001t0002g0033a0001c0001t0002g0096others(4): Show | 9 | HG00673.hp2 HG02132.hp2 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.52-713A>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36281550 | ||||||
chr11:36281719
|
A | G | 1 | a0001c0001t0003g0212 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.52-882T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36281719 | ||||||
chr11:36281826
|
C | G | 1 | a0001c0001t0002g0110 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.52-989G>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36281826 | ||||||
chr11:36281907
|
C | T | 16 | a0001c0001t0005g0036a0001c0001t0005g0064a0001c0001t0005g0140others(13): Show | 18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.52-1070G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36281907 | ||||||
chr11:36281920
|
T | C | 40 | a0001c0001t0001g0019a0001c0001t0001g0047a0001c0001t0001g0048others(37): Show | 49 | HG00323.hp1 HG00609.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.52-1083A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36281920 | ||||||
chr11:36281959
|
C | A | 16 | a0001c0001t0005g0036a0001c0001t0005g0064a0001c0001t0005g0140others(13): Show | 18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.52-1122G>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36281959 | ||||||
chr11:36282152
|
C | T | 1 | a0001c0001t0004g0195 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.52-1315G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36282152 | ||||||
chr11:36282388
|
A | G | 1 | a0001c0001t0001g0054 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.52-1551T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36282388 | ||||||
chr11:36282413
|
C | A | 1 | a0001c0001t0001g0186 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.52-1576G>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36282413 | ||||||
chr11:36282462
|
A | G | 16 | a0001c0001t0005g0036a0001c0001t0005g0064a0001c0001t0005g0140others(13): Show | 18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.52-1625T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36282462 | ||||||
chr11:36282463
|
AAACCATG others(25): Show |
A | 1 | a0001c0001t0005g0150 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.52-1658_52-1627del others(32): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36282463 | ||||||
chr11:36282513
|
G | GA | 18 | a0001c0001t0001g0170a0001c0001t0003g0214a0001c0001t0005g0036others(15): Show | 20 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.52-1677dupT | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36282513 | ||||||
chr11:36282581
|
G | A | 1 | a0001c0001t0005g0149 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.52-1744C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36282581 | ||||||
chr11:36282701
|
A | G | 1 | a0001c0001t0001g0231 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.52-1864T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36282701 | ||||||
chr11:36282731
|
G | A | 16 | a0001c0001t0005g0036a0001c0001t0005g0064a0001c0001t0005g0140others(13): Show | 18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.52-1894C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36282731 | ||||||
chr11:36282792
|
G | T | 1 | a0001c0001t0001g0173 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.52-1955C>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36282792 | ||||||
chr11:36282793
|
G | C | 1 | a0001c0001t0001g0173 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.52-1956C>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36282793 | ||||||
chr11:36282795
|
A | G | 1 | a0001c0001t0001g0173 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.52-1958T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36282795 | ||||||
chr11:36282796
|
A | C | 1 | a0001c0001t0001g0173 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.52-1959T>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36282796 | ||||||
chr11:36283101
|
A | G | 16 | a0001c0001t0005g0036a0001c0001t0005g0064a0001c0001t0005g0140others(13): Show | 18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.52-2264T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36283101 | ||||||
chr11:36283190
|
C | T | 16 | a0001c0001t0005g0036a0001c0001t0005g0064a0001c0001t0005g0140others(13): Show | 18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.52-2353G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36283190 | ||||||
chr11:36283262
|
A | G | 1 | a0001c0001t0001g0300 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.52-2425T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36283262 | ||||||
chr11:36283401
|
G | A | 7 | a0001c0001t0001g0267a0001c0001t0001g0273a0001c0001t0001g0274others(4): Show | 7 | HG00741.hp1 HG01928.hp2 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.52-2564C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36283401 | ||||||
chr11:36283482
|
T | C | 1 | a0001c0001t0013g0187 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.52-2645A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36283482 | ||||||
chr11:36283604
|
A | T | 1 | a0001c0001t0004g0312 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.52-2767T>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36283604 | ||||||
chr11:36283674
|
G | T | 24 | a0001c0001t0001g0186a0001c0001t0001g0213a0001c0001t0003g0001others(21): Show | 50 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.52-2837C>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36283674 | ||||||
chr11:36283957
|
T | G | 1 | a0001c0001t0017g0317 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.52-3120A>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36283957 | ||||||
chr11:36284104
|
T | TCAA | 86 | a0001c0001t0001g0007a0001c0001t0001g0186a0001c0001t0001g0225others(83): Show | 110 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.52-3270_52-3268dup others(3): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36284104 | ||||||
chr11:36284104
|
T | TCAACAA | 28 | a0001c0001t0001g0213a0001c0001t0002g0071a0001c0001t0002g0082others(25): Show | 31 | HG00438.hp2 HG00597.hp1 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.52-3273_52-3268dup others(6): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36284104 | ||||||
chr11:36284104
|
TCAA | T | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(121): Show | 209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.52-3270_52-3268del others(3): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36284104 | ||||||
chr11:36284104
|
TCAACAA | T | 7 | a0001c0001t0001g0061a0001c0001t0001g0139a0001c0001t0001g0285others(4): Show | 8 | HG01070.hp1 HG01071.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.52-3273_52-3268del others(6): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36284104 | ||||||
chr11:36284104
|
TCAACAAC others(5): Show |
T | 2 | a0001c0001t0003g0217a0001c0001t0003g0219 | 2 | NA18964.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.52-3279_52-3268del others(12): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36284104 | ||||||
chr11:36284104
|
TCAACAAC others(8): Show |
T | 2 | a0001c0001t0001g0297a0001c0001t0001g0298 | 2 | HG01109.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.52-3282_52-3268del others(15): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36284104 | ||||||
chr11:36284300
|
G | A | 1 | a0001c0001t0001g0304 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.52-3463C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36284300 | ||||||
chr11:36284406
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.52-3569C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36284406 | ||||||
chr11:36284652
|
G | C | 5 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(2): Show | 5 | HG02055.hp2 HG02280.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.52-3815C>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36284652 | ||||||
chr11:36284712
|
T | C | 5 | a0001c0001t0002g0031a0001c0001t0002g0097a0001c0001t0002g0102others(2): Show | 6 | HG00735.hp2 HG01192.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.52-3875A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36284712 | ||||||
chr11:36284988
|
A | G | 100 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0012others(97): Show | 137 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.52-4151T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36284988 | ||||||
chr11:36285605
|
G | A | 2 | a0001c0001t0005g0148a0001c0001t0005g0151 | 2 | HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.51+3757C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36285605 | ||||||
chr11:36285745
|
A | G | 5 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(2): Show | 5 | HG02055.hp2 HG02280.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.51+3617T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36285745 | ||||||
chr11:36285791
|
C | T | 24 | a0001c0001t0001g0186a0001c0001t0001g0213a0001c0001t0003g0001others(21): Show | 50 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.51+3571G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36285791 | ||||||
chr11:36285793
|
T | A | 37 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(34): Show | 67 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(64): Show |
intron_variant | MODIFIER | c.51+3569A>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36285793 | ||||||
chr11:36285797
|
A | G | 102 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0012others(99): Show | 139 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.51+3565T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36285797 | ||||||
chr11:36285806
|
T | C | 15 | a0001c0001t0001g0152a0001c0001t0005g0036a0001c0001t0005g0064others(12): Show | 17 | HG00438.hp2 HG00733.hp2 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.51+3556A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36285806 | ||||||
chr11:36285867
|
G | C | 15 | a0001c0001t0001g0152a0001c0001t0005g0036a0001c0001t0005g0064others(12): Show | 17 | HG00438.hp2 HG00733.hp2 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.51+3495C>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36285867 | ||||||
chr11:36285972
|
A | G | 82 | a0001c0001t0002g0006a0001c0001t0002g0024a0001c0001t0002g0025others(79): Show | 99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+3390T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36285972 | ||||||
chr11:36285973
|
G | C | 82 | a0001c0001t0002g0006a0001c0001t0002g0024a0001c0001t0002g0025others(79): Show | 99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+3389C>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36285973 | ||||||
chr11:36286046
|
CAAGGAAA others(139): Show |
C | 1 | a0001c0001t0001g0225 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.51+3170_51+3315del | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286046 | ||||||
chr11:36286050
|
G | A | 7 | a0001c0001t0001g0267a0001c0001t0001g0273a0001c0001t0001g0274others(4): Show | 7 | HG00741.hp1 HG01928.hp2 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.51+3312C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286050 | ||||||
chr11:36286395
|
C | CAA | 104 | a0001c0001t0001g0019a0001c0001t0001g0047a0001c0001t0001g0048others(101): Show | 128 | HG00323.hp1 HG00544.hp2 HG00597.hp1 others(125): Show |
intron_variant | MODIFIER | c.51+2965_51+2966dup others(2): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286395 | ||||||
chr11:36286395
|
C | CAAA | 10 | a0001c0001t0001g0157a0001c0001t0001g0183a0001c0001t0001g0238others(7): Show | 12 | HG01981.hp1 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.51+2964_51+2966dup others(3): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286395 | ||||||
chr11:36286395
|
C | CAAAA | 28 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(25): Show | 54 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(51): Show |
intron_variant | MODIFIER | c.51+2963_51+2966dup others(4): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286395 | ||||||
chr11:36286395
|
C | CAAAAA | 5 | a0001c0001t0001g0017a0001c0001t0001g0166a0001c0001t0001g0175others(2): Show | 7 | HG01070.hp2 HG01358.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.51+2962_51+2966dup others(5): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286395 | ||||||
chr11:36286395
|
CA | C | 13 | a0001c0001t0001g0152a0001c0001t0005g0036a0001c0001t0005g0064others(10): Show | 15 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.51+2966delT | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286395 | ||||||
chr11:36286408
|
AAAAAAGA others(11): Show |
A | 17 | a0001c0001t0004g0011a0001c0001t0004g0041a0001c0001t0004g0042others(14): Show | 22 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.51+2936_51+2953del others(18): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286408 | ||||||
chr11:36286409
|
AAAAAGAA others(10): Show |
A | 9 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(6): Show | 9 | HG00621.hp1 HG01928.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.51+2936_51+2952del others(17): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286409 | ||||||
chr11:36286410
|
A | AAAAAAAG others(4): Show |
1 | a0001c0001t0001g0234 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.51+2951_51+2952ins others(11): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286410 | ||||||
chr11:36286410
|
A | AAAAAAG | 6 | a0001c0001t0001g0158a0001c0001t0001g0160a0001c0001t0001g0161others(3): Show | 6 | HG00280.hp1 HG01358.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.51+2951_51+2952ins others(6): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286410 | ||||||
chr11:36286410
|
A | AAAG | 2 | a0001c0001t0001g0007a0001c0001t0001g0163 | 7 | HG01261.hp1 HG02809.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.51+2951_51+2952ins others(3): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286410 | ||||||
chr11:36286410
|
AAAAGAAA others(9): Show |
A | 68 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0012others(65): Show | 94 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.51+2936_51+2951del others(16): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286410 | ||||||
chr11:36286411
|
AAAGAAAG others(8): Show |
A | 7 | a0001c0001t0001g0060a0001c0001t0001g0063a0001c0001t0001g0139others(4): Show | 13 | HG00642.hp2 HG00735.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.51+2936_51+2950del others(15): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286411 | ||||||
chr11:36286412
|
AAGAAAG | A | 6 | a0001c0001t0001g0159a0001c0001t0006g0131a0001c0001t0006g0135others(3): Show | 6 | HG02109.hp1 HG02280.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.51+2944_51+2949del others(6): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286412 | ||||||
chr11:36286412
|
AAGAAAGA others(3): Show |
A | 1 | a0001c0001t0002g0127 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.51+2940_51+2949del others(10): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286412 | ||||||
chr11:36286414
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0172 | 4 | NA18954.hp2 NA18969.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+2948C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286414 | ||||||
chr11:36286427
|
AAAG | A | 22 | a0001c0001t0001g0186a0001c0001t0001g0213a0001c0001t0003g0001others(19): Show | 47 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.51+2932_51+2934del others(3): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286427 | ||||||
chr11:36286435
|
AAAAG | A | 22 | a0001c0001t0001g0186a0001c0001t0001g0213a0001c0001t0003g0001others(19): Show | 47 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.51+2923_51+2926del others(4): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286435 | ||||||
chr11:36286438
|
A | G | 2 | a0002c0002t0006g0077a0002c0002t0006g0078 | 2 | HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.51+2924T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286438 | ||||||
chr11:36286439
|
G | A | 2 | a0002c0002t0006g0077a0002c0002t0006g0078 | 2 | HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.51+2923C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286439 | ||||||
chr11:36286439
|
G | GA | 164 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(161): Show | 222 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.51+2922dupT | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286439 | ||||||
chr11:36286443
|
A | G | 2 | a0002c0002t0006g0077a0002c0002t0006g0078 | 2 | HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.51+2919T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286443 | ||||||
chr11:36286463
|
G | C | 5 | a0001c0001t0001g0048a0001c0001t0001g0051a0001c0001t0001g0239others(2): Show | 7 | HG02257.hp1 HG02572.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.51+2899C>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286463 | ||||||
chr11:36286506
|
T | C | 1 | a0001c0001t0002g0035 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.51+2856A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286506 | ||||||
chr11:36286597
|
A | AAAAC | 4 | a0001c0001t0001g0152a0001c0001t0003g0221a0001c0001t0003g0222others(1): Show | 4 | HG01243.hp2 HG02004.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+2761_51+2764dup others(4): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286597 | ||||||
chr11:36286623
|
A | C | 1 | a0001c0001t0002g0095 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.51+2739T>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286623 | ||||||
chr11:36286643
|
G | A | 1 | a0001c0001t0002g0127 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.51+2719C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286643 | ||||||
chr11:36286705
|
T | C | 24 | a0001c0001t0001g0186a0001c0001t0001g0213a0001c0001t0003g0001others(21): Show | 50 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.51+2657A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286705 | ||||||
chr11:36286743
|
A | C | 1 | a0001c0001t0002g0076 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.51+2619T>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286743 | ||||||
chr11:36286755
|
T | C | 103 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0012others(100): Show | 140 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.51+2607A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286755 | ||||||
chr11:36286891
|
G | A | 2 | a0001c0001t0002g0091a0001c0001t0002g0092 | 2 | NA18940.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.51+2471C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286891 | ||||||
chr11:36286903
|
A | C | 3 | a0001c0001t0001g0314a0001c0001t0001g0315a0001c0001t0001g0316 | 3 | HG01243.hp1 HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.51+2459T>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286903 | ||||||
chr11:36286916
|
C | G | 1 | a0001c0001t0003g0218 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.51+2446G>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286916 | ||||||
chr11:36286940
|
T | C | 2 | a0001c0001t0001g0157a0001c0001t0001g0183 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.51+2422A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286940 | ||||||
chr11:36286947
|
ACTGTCAA others(57): Show |
A | 1 | a0001c0001t0005g0142 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.51+2351_51+2414del others(64): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36286947 | ||||||
chr11:36287046
|
A | ATATGTAT others(153): Show |
3 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0013g0187 | 3 | HG01081.hp2 HG02145.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(160): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | ||||||
chr11:36287046
|
A | ATATGTAT others(217): Show |
4 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(1): Show | 4 | HG01361.hp2 HG02074.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(224): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | ||||||
chr11:36287046
|
A | ATATGTAT others(249): Show |
5 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0068others(2): Show | 13 | HG00099.hp2 HG00423.hp2 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(256): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | ||||||
chr11:36287046
|
A | ATATGTAT others(281): Show |
8 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0039others(5): Show | 17 | HG01167.hp1 HG01255.hp1 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(288): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | ||||||
chr11:36287046
|
A | ATATGTAT others(313): Show |
9 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0154others(6): Show | 18 | HG00140.hp1 HG00140.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(320): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | ||||||
chr11:36287046
|
A | ATATGTAT others(345): Show |
9 | a0001c0001t0001g0023a0001c0001t0001g0038a0001c0001t0001g0065others(6): Show | 13 | HG01123.hp2 HG01515.hp1 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(352): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | ||||||
chr11:36287046
|
A | ATATGTAT others(377): Show |
10 | a0001c0001t0001g0037a0001c0001t0001g0167a0001c0001t0001g0168others(7): Show | 15 | HG00621.hp2 HG01123.hp1 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(384): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | ||||||
chr11:36287046
|
A | ATATGTAT others(409): Show |
4 | a0001c0001t0003g0001a0001c0001t0003g0044a0001c0001t0003g0216others(1): Show | 18 | HG00609.hp1 HG01993.hp2 HG02083.hp1 others(15): Show |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(416): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | ||||||
chr11:36287046
|
A | ATATGTAT others(441): Show |
3 | a0001c0001t0001g0166a0001c0001t0003g0008a0001c0001t0003g0318 | 7 | HG00408.hp2 HG01978.hp1 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(448): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | ||||||
chr11:36287046
|
A | ATATGTAT others(1579): Show |
1 | a0001c0001t0001g0225 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.51+2315_51+2316ins others(1586): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | ||||||
chr11:36287046
|
A | ATATGTAT others(505): Show |
1 | a0001c0001t0003g0043 | 2 | NA18986.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(512): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | ||||||
chr11:36287046
|
A | ATATGTAT others(537): Show |
1 | a0001c0001t0003g0215 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.51+2315_51+2316ins others(544): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | ||||||
chr11:36287046
|
A | ATATGTAT others(789): Show |
1 | a0001c0001t0001g0250 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.51+2315_51+2316ins others(796): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | ||||||
chr11:36287046
|
A | ATATGTAT others(569): Show |
1 | a0001c0001t0001g0053 | 2 | HG01975.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(576): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | ||||||
chr11:36287046
|
A | ATATGTAT others(601): Show |
2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG01192.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(608): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | ||||||
chr11:36287046
|
A | ATATGTAT others(633): Show |
2 | a0001c0001t0001g0019a0001c0001t0003g0214 | 4 | HG02165.hp2 HG03130.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(640): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | ||||||
chr11:36287046
|
A | ATATGTAT others(665): Show |
1 | a0001c0001t0001g0247 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.51+2315_51+2316ins others(672): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | ||||||
chr11:36287046
|
A | ATATGTAT others(697): Show |
3 | a0001c0001t0001g0052a0001c0001t0001g0246a0001c0001t0016g0245 | 4 | HG02886.hp2 NA18906.hp2 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(704): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | ||||||
chr11:36287046
|
A | ATATGTAT others(729): Show |
3 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244 | 3 | HG03540.hp1 HG03710.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(736): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | ||||||
chr11:36287046
|
A | ATATGTAT others(761): Show |
3 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0192 | 5 | HG01099.hp2 HG01361.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(768): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | ||||||
chr11:36287046
|
A | ATATGTAT others(793): Show |
2 | a0001c0001t0001g0049a0001c0001t0001g0191 | 3 | HG00733.hp1 HG01256.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(800): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | ||||||
chr11:36287046
|
A | ATATGTAT others(825): Show |
4 | a0001c0001t0001g0048a0001c0001t0001g0190a0001c0001t0001g0240others(1): Show | 5 | HG01255.hp2 HG01952.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(832): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | ||||||
chr11:36287046
|
A | ATATGTAT others(857): Show |
2 | a0001c0001t0001g0238a0001c0001t0001g0239 | 2 | HG01981.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(864): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | ||||||
chr11:36287046
|
A | ATATGTAT others(921): Show |
1 | a0001c0001t0001g0237 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.51+2315_51+2316ins others(928): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | ||||||
chr11:36287046
|
A | ATATGTAT others(985): Show |
2 | a0001c0001t0001g0235a0001c0001t0001g0236 | 2 | HG03209.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(992): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | ||||||
chr11:36287046
|
A | ATATGTAT others(1017): Show |
2 | a0001c0001t0001g0047a0001c0001t0001g0234 | 3 | HG01081.hp1 HG02300.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(1024): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | ||||||
chr11:36287046
|
A | ATATGTAT others(1049): Show |
1 | a0001c0001t0001g0189 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.51+2315_51+2316ins others(1056): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | ||||||
chr11:36287046
|
A | ATATGTAT others(1081): Show |
2 | a0001c0001t0001g0224a0001c0001t0001g0233 | 2 | HG02630.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(1088): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | ||||||
chr11:36287046
|
A | ATATGTAT others(1145): Show |
3 | a0001c0001t0001g0188a0001c0001t0001g0231a0001c0001t0001g0232 | 3 | HG00609.hp2 HG04199.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(1152): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | ||||||
chr11:36287046
|
A | ATATGTAT others(1177): Show |
2 | a0001c0001t0001g0229a0001c0005t0001g0230 | 2 | HG03942.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(1184): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | ||||||
chr11:36287046
|
A | ATATGTAT others(1273): Show |
1 | a0001c0001t0001g0228 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.51+2315_51+2316ins others(1280): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | ||||||
chr11:36287046
|
A | ATATGTAT others(1305): Show |
1 | a0001c0001t0001g0227 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.51+2315_51+2316ins others(1312): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | ||||||
chr11:36287046
|
A | ATATGTAT others(1849): Show |
1 | a0001c0001t0001g0226 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.51+2315_51+2316ins others(1856): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | ||||||
chr11:36287046
|
A | ATATGTAT others(313): Show |
1 | a0001c0001t0001g0165 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.51+2315_51+2316ins others(320): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | ||||||
chr11:36287046
|
A | ATATGTAT others(313): Show |
1 | a0001c0001t0001g0164 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.51+2315_51+2316ins others(320): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | ||||||
chr11:36287046
|
A | ATATGTAT others(441): Show |
2 | a0001c0001t0001g0007a0001c0001t0001g0163 | 7 | HG01261.hp1 HG02809.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.51+2315_51+2316ins others(448): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | ||||||
chr11:36287046
|
A | ATATGTAT others(1145): Show |
1 | a0001c0001t0001g0316 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.51+2315_51+2316ins others(1152): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | ||||||
chr11:36287046
|
A | ATATGTAT others(1209): Show |
1 | a0001c0001t0001g0315 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.51+2315_51+2316ins others(1216): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | ||||||
chr11:36287046
|
A | ATATGTAT others(1273): Show |
1 | a0001c0001t0001g0314 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.51+2315_51+2316ins others(1280): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | ||||||
chr11:36287046
|
A | ATATGTAT others(1465): Show |
1 | a0001c0001t0005g0149 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.51+2315_51+2316ins others(1472): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287046 | ||||||
chr11:36287054
|
A | ACTACATA others(697): Show |
1 | a0001c0001t0005g0150 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.51+2307_51+2308ins others(704): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287054 | ||||||
chr11:36287054
|
A | ACTACATA others(761): Show |
1 | a0001c0001t0005g0064 | 2 | HG00438.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.51+2307_51+2308ins others(768): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287054 | ||||||
chr11:36287054
|
A | ACTACATA others(1145): Show |
1 | a0001c0001t0005g0036 | 2 | HG03710.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.51+2307_51+2308ins others(1152): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287054 | ||||||
chr11:36287054
|
A | ACTACATA others(1177): Show |
1 | a0001c0001t0005g0143 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.51+2307_51+2308ins others(1184): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287054 | ||||||
chr11:36287054
|
A | ACTACATA others(1273): Show |
1 | a0001c0001t0005g0142 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.51+2307_51+2308ins others(1280): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287054 | ||||||
chr11:36287054
|
A | ACTACATA others(1305): Show |
1 | a0001c0001t0005g0140 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.51+2307_51+2308ins others(1312): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287054 | ||||||
chr11:36287054
|
A | ACTACATA others(1433): Show |
1 | a0001c0001t0005g0141 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.51+2307_51+2308ins others(1440): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287054 | ||||||
chr11:36287054
|
A | ACTACATA others(1817): Show |
1 | a0001c0001t0005g0145 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.51+2307_51+2308ins others(1824): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287054 | ||||||
chr11:36287054
|
A | ACTACATA others(1945): Show |
1 | a0001c0001t0005g0148 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.51+2307_51+2308ins others(1952): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287054 | ||||||
chr11:36287054
|
A | ACTACATA others(2233): Show |
1 | a0001c0001t0005g0147 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.51+2307_51+2308ins others(2240): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287054 | ||||||
chr11:36287054
|
A | ACTACATA others(2841): Show |
1 | a0001c0001t0005g0146 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.51+2307_51+2308ins others(2848): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287054 | ||||||
chr11:36287054
|
A | G | 1 | a0001c0001t0005g0149 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.51+2308T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287054 | ||||||
chr11:36287056
|
T | TACATACT others(505): Show |
3 | a0001c0001t0007g0040a0001c0001t0007g0193a0001c0004t0007g0194 | 4 | HG02895.hp2 HG02965.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+2305_51+2306ins others(512): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287056 | ||||||
chr11:36287056
|
T | TACATACT others(537): Show |
1 | a0001c0001t0007g0184 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.51+2305_51+2306ins others(544): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287056 | ||||||
chr11:36287061
|
A | ACTATGTA others(313): Show |
1 | a0002c0002t0006g0078 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.51+2300_51+2301ins others(320): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287061 | ||||||
chr11:36287061
|
A | ACTATGTA others(345): Show |
2 | a0001c0001t0002g0113a0002c0002t0006g0077 | 2 | HG02056.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.51+2300_51+2301ins others(352): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287061 | ||||||
chr11:36287061
|
A | ACTATGTA others(755): Show |
1 | a0001c0001t0002g0083 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.51+2300_51+2301ins others(762): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287061 | ||||||
chr11:36287061
|
A | ACTATGTA others(726): Show |
1 | a0001c0001t0002g0121 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.51+2300_51+2301ins others(733): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287061 | ||||||
chr11:36287061
|
A | ACTATGTA others(790): Show |
1 | a0001c0001t0002g0075 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.51+2300_51+2301ins others(797): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287061 | ||||||
chr11:36287061
|
A | ACTATGTA others(726): Show |
1 | a0001c0001t0002g0126 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.51+2300_51+2301ins others(733): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287061 | ||||||
chr11:36287061
|
A | ACTATGTA others(822): Show |
3 | a0001c0001t0002g0031a0001c0001t0002g0107a0001c0001t0002g0108 | 4 | HG01256.hp2 HG01258.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+2300_51+2301ins others(829): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287061 | ||||||
chr11:36287061
|
A | ACTATGTA others(854): Show |
1 | a0001c0001t0002g0099 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.51+2300_51+2301ins others(861): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287061 | ||||||
chr11:36287061
|
A | ACTATGTA others(758): Show |
1 | a0001c0001t0002g0125 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.51+2300_51+2301ins others(765): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287061 | ||||||
chr11:36287061
|
A | ACTATGTA others(854): Show |
1 | a0001c0001t0002g0102 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.51+2300_51+2301ins others(861): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287061 | ||||||
chr11:36287061
|
A | ACTATGTA others(886): Show |
1 | a0001c0001t0002g0097 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.51+2300_51+2301ins others(893): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287061 | ||||||
chr11:36287061
|
A | ACTATGTA others(505): Show |
1 | a0001c0001t0006g0138 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.51+2300_51+2301ins others(512): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287061 | ||||||
chr11:36287061
|
A | ACTATGTA others(854): Show |
1 | a0001c0001t0002g0115 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.51+2300_51+2301ins others(861): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287061 | ||||||
chr11:36287061
|
A | ACTATGTA others(537): Show |
2 | a0001c0001t0006g0136a0001c0001t0006g0137 | 2 | HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.51+2300_51+2301ins others(544): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287061 | ||||||
chr11:36287061
|
A | ACTATGTA others(569): Show |
1 | a0001c0001t0006g0135 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.51+2300_51+2301ins others(576): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287061 | ||||||
chr11:36287061
|
A | ACTATGTA others(537): Show |
1 | a0001c0001t0006g0131 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.51+2300_51+2301ins others(544): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287061 | ||||||
chr11:36287069
|
T | C | 82 | a0001c0001t0002g0006a0001c0001t0002g0024a0001c0001t0002g0025others(79): Show | 99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+2293A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287069 | ||||||
chr11:36287073
|
G | A | 312 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(309): Show | 434 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(431): Show |
intron_variant | MODIFIER | c.51+2289C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287073 | ||||||
chr11:36287074
|
C | T | 312 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(309): Show | 434 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(431): Show |
intron_variant | MODIFIER | c.51+2288G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287074 | ||||||
chr11:36287075
|
G | A | 218 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(215): Show | 304 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.51+2287C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287075 | ||||||
chr11:36287075
|
G | ATAGCATG others(217): Show |
1 | a0001c0001t0004g0199 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.51+2287_51+2288ins others(224): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287075 | ||||||
chr11:36287075
|
G | ATAGCATG others(281): Show |
1 | a0001c0001t0004g0198 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.51+2287_51+2288ins others(288): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287075 | ||||||
chr11:36287075
|
G | ATAGCATG others(313): Show |
5 | a0001c0001t0004g0197a0001c0001t0004g0206a0001c0001t0004g0207others(2): Show | 5 | HG00621.hp1 NA18952.hp1 NA19006.hp1 others(2): Show |
intron_variant | MODIFIER | c.51+2287_51+2288ins others(320): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287075 | ||||||
chr11:36287075
|
G | ATAGCATG others(345): Show |
1 | a0001c0001t0004g0196 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.51+2287_51+2288ins others(352): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287075 | ||||||
chr11:36287075
|
G | ATAGCATG others(377): Show |
2 | a0001c0001t0004g0042a0001c0001t0004g0195 | 3 | HG01981.hp2 HG02080.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.51+2287_51+2288ins others(384): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287075 | ||||||
chr11:36287075
|
G | ATAGCATG others(409): Show |
1 | a0001c0001t0004g0011 | 4 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+2287_51+2288ins others(416): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287075 | ||||||
chr11:36287075
|
G | ATAGCATG others(473): Show |
1 | a0001c0001t0004g0205 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.51+2287_51+2288ins others(480): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287075 | ||||||
chr11:36287076
|
T | TAGCATGT others(313): Show |
1 | a0001c0001t0004g0202 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.51+2285_51+2286ins others(320): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287076 | ||||||
chr11:36287076
|
T | TAGCATGT others(313): Show |
2 | a0001c0001t0004g0041a0001c0001t0004g0200 | 3 | NA18945.hp2 NA18995.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.51+2285_51+2286ins others(320): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287076 | ||||||
chr11:36287076
|
T | TAGCATGT others(345): Show |
1 | a0001c0001t0004g0201 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.51+2285_51+2286ins others(352): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287076 | ||||||
chr11:36287079
|
T | C | 20 | a0001c0001t0004g0011a0001c0001t0004g0041a0001c0001t0004g0042others(17): Show | 25 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.51+2283A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287079 | ||||||
chr11:36287086
|
A | G | 16 | a0001c0001t0005g0036a0001c0001t0005g0064a0001c0001t0005g0140others(13): Show | 18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.51+2276T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287086 | ||||||
chr11:36287088
|
T | C | 4 | a0001c0001t0007g0040a0001c0001t0007g0184a0001c0001t0007g0193others(1): Show | 5 | HG02451.hp1 HG02895.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.51+2274A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287088 | ||||||
chr11:36287088
|
T | TACAATGT others(781): Show |
1 | a0001c0001t0001g0265 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.51+2273_51+2274ins others(788): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287088 | ||||||
chr11:36287088
|
T | TACAATGT others(1009): Show |
1 | a0001c0001t0001g0293 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.51+2273_51+2274ins others(1016): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287088 | ||||||
chr11:36287088
|
T | TACAATGT others(909): Show |
1 | a0001c0001t0001g0282 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.51+2273_51+2274ins others(916): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287088 | ||||||
chr11:36287093
|
A | ACTATGTA others(249): Show |
1 | a0001c0001t0002g0127 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(256): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287093
|
A | ACTATGTA others(313): Show |
1 | a0002c0002t0006g0079 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(320): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287093
|
A | ACTATGTA others(726): Show |
1 | a0001c0001t0002g0118 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(733): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287093
|
A | ACTATGTA others(819): Show |
1 | a0001c0001t0002g0112 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(826): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287093
|
A | ACTATGTA others(851): Show |
1 | a0001c0001t0002g0101 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(858): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287093
|
A | ACTATGTA others(630): Show |
2 | a0001c0001t0002g0076a0001c0001t0002g0128 | 2 | NA18984.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.51+2268_51+2269ins others(637): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287093
|
A | ACTATGTA others(758): Show |
1 | a0001c0001t0002g0117 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(765): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287093
|
A | ACTATGTA others(790): Show |
3 | a0001c0001t0002g0034a0001c0001t0002g0110a0001c0001t0002g0111 | 4 | HG00597.hp2 NA18966.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+2268_51+2269ins others(797): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287093
|
A | ACTATGTA others(950): Show |
1 | a0001c0001t0002g0092 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(957): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287093
|
A | ACTATGTA others(787): Show |
1 | a0001c0001t0002g0122 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(794): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287093
|
A | ACTATGTA others(758): Show |
1 | a0001c0001t0002g0120 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(765): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287093
|
A | ACTATGTA others(822): Show |
1 | a0001c0001t0002g0109 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(829): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287093
|
A | ACTATGTA others(854): Show |
3 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0100 | 5 | HG02027.hp1 HG02135.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.51+2268_51+2269ins others(861): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287093
|
A | ACTATGTA others(982): Show |
1 | a0001c0001t0002g0091 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(989): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287093
|
A | ACTATGTA others(441): Show |
1 | a0001c0001t0002g0096 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(448): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287093
|
A | ACTATGTA others(851): Show |
1 | a0001c0001t0002g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(858): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287093
|
A | ACTATGTA others(947): Show |
1 | a0001c0001t0002g0026 | 2 | HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.51+2268_51+2269ins others(954): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287093
|
A | ACTATGTA others(758): Show |
2 | a0001c0001t0002g0033a0001c0001t0002g0080 | 3 | HG03017.hp2 NA18978.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.51+2268_51+2269ins others(765): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287093
|
A | ACTATGTA others(790): Show |
1 | a0001c0001t0002g0119 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(797): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287093
|
A | ACTATGTA others(854): Show |
5 | a0001c0001t0002g0030a0001c0001t0002g0103a0001c0001t0002g0104others(2): Show | 6 | HG00438.hp1 HG01192.hp1 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.51+2268_51+2269ins others(861): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287093
|
A | ACTATGTA others(886): Show |
1 | a0001c0001t0002g0098 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(893): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287093
|
A | ACTATGTA others(982): Show |
2 | a0001c0001t0008g0074a0001c0001t0008g0094 | 2 | NA18939.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.51+2268_51+2269ins others(989): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287093
|
A | ACTATGTA others(1078): Show |
1 | a0001c0001t0002g0090 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(1085): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287093
|
A | ACTATGTA others(851): Show |
1 | a0001c0001t0002g0071 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(858): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287093
|
A | ACTATGTA others(915): Show |
1 | a0001c0001t0002g0070 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(922): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287093
|
A | ACTATGTA others(1043): Show |
1 | a0001c0001t0002g0081 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(1050): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287093
|
A | ACTATGTA others(790): Show |
2 | a0001c0001t0002g0032a0001c0001t0002g0124 | 3 | NA18943.hp1 NA18983.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.51+2268_51+2269ins others(797): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287093
|
A | ACTATGTA others(854): Show |
1 | a0001c0001t0002g0116 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(861): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287093
|
A | ACTATGTA others(886): Show |
2 | a0001c0001t0002g0006a0001c0001t0002g0024 | 8 | HG00544.hp2 NA18946.hp1 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.51+2268_51+2269ins others(893): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287093
|
A | ACTATGTA others(1014): Show |
1 | a0001c0001t0008g0093 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(1021): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287093
|
A | ACTATGTA others(505): Show |
1 | a0001c0001t0002g0095 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(512): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287093
|
A | ACTATGTA others(883): Show |
1 | a0001c0001t0002g0082 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(890): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287093
|
A | ACTATGTA others(822): Show |
1 | a0001c0001t0002g0123 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(829): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287093
|
A | ACTATGTA others(761): Show |
1 | a0001c0001t0002g0073 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(768): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287093
|
A | ACTATGTA others(857): Show |
2 | a0001c0001t0002g0035a0001c0001t0002g0087 | 3 | HG02886.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.51+2268_51+2269ins others(864): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287093
|
A | ACTATGTA others(889): Show |
1 | a0001c0001t0002g0130 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(896): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287093
|
A | ACTATGTA others(921): Show |
2 | a0001c0001t0002g0086a0001c0001t0002g0134 | 2 | HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.51+2268_51+2269ins others(928): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287093
|
A | ACTATGTA others(985): Show |
1 | a0001c0001t0002g0129 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(992): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287093
|
A | ACTATGTA others(1017): Show |
1 | a0001c0001t0002g0027 | 2 | NA19070.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.51+2268_51+2269ins others(1024): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287093
|
A | ACTATGTA others(1081): Show |
1 | a0001c0001t0002g0085 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(1088): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287093
|
A | ACTATGTA others(1113): Show |
1 | a0001c0001t0002g0084 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.51+2268_51+2269ins others(1120): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287093
|
A | ACTATGTA others(1145): Show |
1 | a0001c0001t0002g0025 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.51+2268_51+2269ins others(1152): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287093
|
A | G | 20 | a0001c0001t0002g0031a0001c0001t0002g0075a0001c0001t0002g0083others(17): Show | 21 | HG00280.hp1 HG01256.hp2 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.51+2269T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287093 | ||||||
chr11:36287094
|
C | CTATGTAC others(873): Show |
1 | a0001c0001t0002g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.51+2267_51+2268ins others(880): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287094 | ||||||
chr11:36287101
|
T | C | 82 | a0001c0001t0002g0006a0001c0001t0002g0024a0001c0001t0002g0025others(79): Show | 99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+2261A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287101 | ||||||
chr11:36287105
|
G | A | 312 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(309): Show | 434 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(431): Show |
intron_variant | MODIFIER | c.51+2257C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287105 | ||||||
chr11:36287106
|
C | T | 312 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(309): Show | 434 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(431): Show |
intron_variant | MODIFIER | c.51+2256G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287106 | ||||||
chr11:36287107
|
G | A | 210 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(207): Show | 295 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.51+2255C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287107 | ||||||
chr11:36287108
|
T | TAGCATGT others(281): Show |
1 | a0001c0001t0004g0204 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.51+2253_51+2254ins others(288): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287108 | ||||||
chr11:36287108
|
T | TAGCATGT others(313): Show |
2 | a0001c0001t0004g0203a0001c0001t0004g0209 | 2 | HG01934.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.51+2253_51+2254ins others(320): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287108 | ||||||
chr11:36287108
|
T | TAGCATGT others(345): Show |
1 | a0001c0001t0004g0210 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.51+2253_51+2254ins others(352): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287108 | ||||||
chr11:36287111
|
T | C | 20 | a0001c0001t0004g0011a0001c0001t0004g0041a0001c0001t0004g0042others(17): Show | 25 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.51+2251A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287111 | ||||||
chr11:36287118
|
A | G | 16 | a0001c0001t0005g0036a0001c0001t0005g0064a0001c0001t0005g0140others(13): Show | 18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.51+2244T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287118 | ||||||
chr11:36287120
|
T | C | 7 | a0001c0001t0001g0265a0001c0001t0001g0282a0001c0001t0001g0293others(4): Show | 8 | HG00280.hp2 HG02451.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.51+2242A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(754): Show |
1 | a0001c0001t0001g0263 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(761): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(789): Show |
1 | a0001c0001t0002g0270 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(796): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(853): Show |
1 | a0001c0001t0001g0278 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(860): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(913): Show |
1 | a0001c0001t0001g0275 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(920): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(945): Show |
1 | a0001c0001t0001g0283 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(952): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(1041): Show |
1 | a0001c0001t0001g0290 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(1048): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(689): Show |
1 | a0001c0001t0004g0302 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(696): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(401): Show |
1 | a0001c0001t0001g0005 | 4 | NA18747.hp2 NA18969.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+2241_51+2242ins others(408): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(561): Show |
1 | a0001c0001t0001g0258 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(568): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(657): Show |
2 | a0001c0001t0001g0308a0001c0001t0004g0020 | 4 | HG00642.hp2 HG01071.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+2241_51+2242ins others(664): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(689): Show |
2 | a0001c0001t0004g0021a0001c0001t0004g0261 | 4 | HG02148.hp2 HG02273.hp1 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+2241_51+2242ins others(696): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(721): Show |
1 | a0001c0001t0004g0312 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(728): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(753): Show |
1 | a0001c0001t0001g0264 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(760): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(785): Show |
1 | a0001c0001t0001g0055 | 2 | HG03492.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.51+2241_51+2242ins others(792): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(817): Show |
2 | a0001c0001t0001g0056a0001c0001t0001g0269 | 3 | HG01099.hp1 HG01106.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.51+2241_51+2242ins others(824): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(881): Show |
2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | NA18945.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.51+2241_51+2242ins others(888): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(913): Show |
1 | a0001c0001t0001g0009 | 5 | HG00558.hp1 HG01943.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.51+2241_51+2242ins others(920): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(945): Show |
2 | a0001c0001t0001g0059a0001c0001t0001g0285 | 3 | HG01433.hp2 HG01515.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.51+2241_51+2242ins others(952): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(977): Show |
4 | a0001c0001t0001g0012a0001c0001t0001g0060a0001c0001t0001g0288others(1): Show | 8 | HG02647.hp2 HG03017.hp1 HG03688.hp1 others(5): Show |
intron_variant | MODIFIER | c.51+2241_51+2242ins others(984): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(1009): Show |
2 | a0001c0001t0001g0292a0001c0001t0010g0291 | 2 | HG02970.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.51+2241_51+2242ins others(1016): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(1041): Show |
3 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0001t0001g0061 | 8 | HG01070.hp1 HG01071.hp1 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.51+2241_51+2242ins others(1048): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(1105): Show |
1 | a0001c0001t0001g0139 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(1112): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(1137): Show |
1 | a0001c0001t0001g0296 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(1144): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(1169): Show |
2 | a0001c0001t0001g0297a0001c0001t0001g0298 | 2 | HG01109.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.51+2241_51+2242ins others(1176): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(1457): Show |
1 | a0001c0001t0001g0062 | 2 | HG01884.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.51+2241_51+2242ins others(1464): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(1489): Show |
1 | a0001c0001t0001g0299 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(1496): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(2033): Show |
1 | a0001c0001t0001g0300 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(2040): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(909): Show |
1 | a0001c0001t0001g0022 | 3 | HG00544.hp1 NA18952.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.51+2241_51+2242ins others(916): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(941): Show |
1 | a0001c0001t0001g0301 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(948): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(397): Show |
1 | a0001c0001t0001g0304 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(404): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(685): Show |
1 | a0001c0001t0001g0259 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(692): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(717): Show |
1 | a0001c0001t0001g0260 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(724): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(749): Show |
1 | a0001c0001t0015g0262 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(756): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(845): Show |
1 | a0001c0001t0001g0267 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(852): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(877): Show |
2 | a0001c0001t0001g0273a0001c0001t0001g0310 | 2 | HG01928.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.51+2241_51+2242ins others(884): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(941): Show |
2 | a0001c0001t0001g0280a0001c0001t0001g0281 | 2 | HG01952.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.51+2241_51+2242ins others(948): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(973): Show |
2 | a0001c0001t0001g0058a0001c0001t0001g0313 | 3 | HG02040.hp1 HG02056.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.51+2241_51+2242ins others(980): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(937): Show |
2 | a0001c0001t0001g0057a0001c0001t0001g0252 | 3 | NA18943.hp2 NA18953.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.51+2241_51+2242ins others(944): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(965): Show |
1 | a0001c0001t0001g0274 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(972): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(753): Show |
1 | a0001c0001t0001g0266 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(760): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(849): Show |
1 | a0001c0001t0001g0254 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(856): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(881): Show |
1 | a0001c0001t0001g0253 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(888): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(913): Show |
1 | a0001c0001t0001g0286 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(920): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(1009): Show |
1 | a0001c0001t0001g0294 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(1016): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(1041): Show |
2 | a0001c0001t0001g0255a0001c0001t0001g0295 | 2 | HG02717.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.51+2241_51+2242ins others(1048): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287120
|
T | TACAATGT others(397): Show |
1 | a0001c0001t0001g0306 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.51+2241_51+2242ins others(404): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287120 | ||||||
chr11:36287123
|
ATACT | A | 11 | a0001c0001t0001g0005a0001c0001t0001g0063a0001c0001t0001g0152others(8): Show | 14 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.51+2235_51+2238del others(4): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287123 | ||||||
chr11:36287125
|
A | ACTATGTA others(761): Show |
1 | a0001c0001t0002g0089 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.51+2236_51+2237ins others(768): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287125 | ||||||
chr11:36287125
|
A | ACTATGTA others(857): Show |
1 | a0001c0001t0002g0088 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.51+2236_51+2237ins others(864): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287125 | ||||||
chr11:36287125
|
A | ACTATGTA others(953): Show |
2 | a0001c0001t0002g0072a0001c0001t0002g0133 | 2 | HG01891.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.51+2236_51+2237ins others(960): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287125 | ||||||
chr11:36287125
|
A | G | 78 | a0001c0001t0002g0006a0001c0001t0002g0024a0001c0001t0002g0025others(75): Show | 95 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.51+2237T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287125 | ||||||
chr11:36287133
|
T | C | 82 | a0001c0001t0002g0006a0001c0001t0002g0024a0001c0001t0002g0025others(79): Show | 99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+2229A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287133 | ||||||
chr11:36287137
|
G | A | 312 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(309): Show | 434 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(431): Show |
intron_variant | MODIFIER | c.51+2225C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287137 | ||||||
chr11:36287138
|
C | T | 312 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(309): Show | 434 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(431): Show |
intron_variant | MODIFIER | c.51+2224G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287138 | ||||||
chr11:36287139
|
G | A | 210 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(207): Show | 295 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.51+2223C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287139 | ||||||
chr11:36287143
|
T | C | 20 | a0001c0001t0004g0011a0001c0001t0004g0041a0001c0001t0004g0042others(17): Show | 25 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.51+2219A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287143 | ||||||
chr11:36287150
|
A | G | 16 | a0001c0001t0005g0036a0001c0001t0005g0064a0001c0001t0005g0140others(13): Show | 18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.51+2212T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287150 | ||||||
chr11:36287152
|
T | C | 71 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0012others(68): Show | 100 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.51+2210A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287152 | ||||||
chr11:36287152
|
T | TACAATGT others(849): Show |
1 | a0001c0001t0001g0268 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.51+2209_51+2210ins others(856): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287152 | ||||||
chr11:36287152
|
T | TACAATGT others(977): Show |
1 | a0001c0001t0001g0284 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.51+2209_51+2210ins others(984): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287152 | ||||||
chr11:36287152
|
T | TACAATGT others(1009): Show |
1 | a0001c0001t0010g0287 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.51+2209_51+2210ins others(1016): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287152 | ||||||
chr11:36287157
|
A | G | 82 | a0001c0001t0002g0006a0001c0001t0002g0024a0001c0001t0002g0025others(79): Show | 99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+2205T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287157 | ||||||
chr11:36287165
|
T | C | 82 | a0001c0001t0002g0006a0001c0001t0002g0024a0001c0001t0002g0025others(79): Show | 99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+2197A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287165 | ||||||
chr11:36287169
|
G | A | 312 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(309): Show | 434 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(431): Show |
intron_variant | MODIFIER | c.51+2193C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287169 | ||||||
chr11:36287170
|
C | T | 312 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(309): Show | 434 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(431): Show |
intron_variant | MODIFIER | c.51+2192G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287170 | ||||||
chr11:36287171
|
G | A | 210 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(207): Show | 295 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.51+2191C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287171 | ||||||
chr11:36287175
|
T | C | 20 | a0001c0001t0004g0011a0001c0001t0004g0041a0001c0001t0004g0042others(17): Show | 25 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.51+2187A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287175 | ||||||
chr11:36287182
|
A | G | 16 | a0001c0001t0005g0036a0001c0001t0005g0064a0001c0001t0005g0140others(13): Show | 18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.51+2180T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287182 | ||||||
chr11:36287184
|
T | C | 75 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0012others(72): Show | 104 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.51+2178A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287184 | ||||||
chr11:36287184
|
T | TACTATGT others(941): Show |
1 | a0001c0001t0001g0279 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.51+2177_51+2178ins others(948): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287184 | ||||||
chr11:36287185
|
A | C | 2 | a0003c0003t0005g0066a0003c0003t0005g0067 | 2 | HG01109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.51+2177T>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287185 | ||||||
chr11:36287189
|
A | G | 82 | a0001c0001t0002g0006a0001c0001t0002g0024a0001c0001t0002g0025others(79): Show | 99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+2173T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287189 | ||||||
chr11:36287197
|
T | C | 82 | a0001c0001t0002g0006a0001c0001t0002g0024a0001c0001t0002g0025others(79): Show | 99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+2165A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287197 | ||||||
chr11:36287201
|
G | A | 312 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(309): Show | 434 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(431): Show |
intron_variant | MODIFIER | c.51+2161C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287201 | ||||||
chr11:36287202
|
C | T | 312 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(309): Show | 434 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(431): Show |
intron_variant | MODIFIER | c.51+2160G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287202 | ||||||
chr11:36287203
|
G | A | 210 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(207): Show | 295 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.51+2159C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287203 | ||||||
chr11:36287207
|
T | C | 20 | a0001c0001t0004g0011a0001c0001t0004g0041a0001c0001t0004g0042others(17): Show | 25 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.51+2155A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287207 | ||||||
chr11:36287214
|
A | G | 16 | a0001c0001t0005g0036a0001c0001t0005g0064a0001c0001t0005g0140others(13): Show | 18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.51+2148T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287214 | ||||||
chr11:36287216
|
T | C | 74 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0012others(71): Show | 103 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.51+2146A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287216 | ||||||
chr11:36287216
|
T | TACTATGT others(405): Show |
2 | a0001c0001t0001g0005a0001c0001t0001g0063 | 5 | NA18949.hp1 NA18955.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.51+2145_51+2146ins others(412): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287216 | ||||||
chr11:36287216
|
T | TACTATGT others(437): Show |
1 | a0001c0001t0001g0307 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.51+2145_51+2146ins others(444): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287216 | ||||||
chr11:36287216
|
T | TACTATGT others(469): Show |
1 | a0001c0001t0001g0257 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.51+2145_51+2146ins others(476): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287216 | ||||||
chr11:36287216
|
T | TACTATGT others(565): Show |
1 | a0001c0001t0001g0251 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.51+2145_51+2146ins others(572): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287216 | ||||||
chr11:36287216
|
T | TACTATGT others(789): Show |
1 | a0001c0001t0001g0309 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.51+2145_51+2146ins others(796): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287216 | ||||||
chr11:36287216
|
T | TACTATGT others(853): Show |
1 | a0001c0001t0001g0311 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.51+2145_51+2146ins others(860): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287216 | ||||||
chr11:36287216
|
T | TACTATGT others(949): Show |
1 | a0001c0001t0001g0152 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.51+2145_51+2146ins others(956): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287216 | ||||||
chr11:36287216
|
T | TACTATGT others(946): Show |
1 | a0001c0001t0001g0256 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.51+2145_51+2146ins others(953): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287216 | ||||||
chr11:36287216
|
T | TACTATGT others(401): Show |
1 | a0001c0001t0001g0303 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.51+2145_51+2146ins others(408): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287216 | ||||||
chr11:36287216
|
T | TACTATGT others(433): Show |
1 | a0001c0001t0001g0305 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.51+2145_51+2146ins others(440): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287216 | ||||||
chr11:36287216
|
T | TACTATGT others(909): Show |
1 | a0001c0001t0001g0272 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.51+2145_51+2146ins others(916): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287216 | ||||||
chr11:36287217
|
A | C | 2 | a0003c0003t0005g0066a0003c0003t0005g0067 | 2 | HG01109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.51+2145T>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287217 | ||||||
chr11:36287221
|
A | G | 82 | a0001c0001t0002g0006a0001c0001t0002g0024a0001c0001t0002g0025others(79): Show | 99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+2141T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287221 | ||||||
chr11:36287229
|
T | C | 82 | a0001c0001t0002g0006a0001c0001t0002g0024a0001c0001t0002g0025others(79): Show | 99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+2133A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287229 | ||||||
chr11:36287233
|
G | A | 312 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(309): Show | 434 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(431): Show |
intron_variant | MODIFIER | c.51+2129C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287233 | ||||||
chr11:36287234
|
C | T | 312 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(309): Show | 434 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(431): Show |
intron_variant | MODIFIER | c.51+2128G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287234 | ||||||
chr11:36287235
|
G | A | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.51+2127C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287235 | ||||||
chr11:36287239
|
T | C | 20 | a0001c0001t0004g0011a0001c0001t0004g0041a0001c0001t0004g0042others(17): Show | 25 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.51+2123A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287239 | ||||||
chr11:36287246
|
A | G | 16 | a0001c0001t0005g0036a0001c0001t0005g0064a0001c0001t0005g0140others(13): Show | 18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.51+2116T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287246 | ||||||
chr11:36287248
|
T | C | 85 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0012others(82): Show | 118 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.51+2114A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287248 | ||||||
chr11:36287248
|
T | TACTATGT others(941): Show |
1 | a0001c0001t0001g0271 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.51+2113_51+2114ins others(948): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287248 | ||||||
chr11:36287249
|
A | C | 2 | a0003c0003t0005g0066a0003c0003t0005g0067 | 2 | HG01109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.51+2113T>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287249 | ||||||
chr11:36287253
|
A | G | 82 | a0001c0001t0002g0006a0001c0001t0002g0024a0001c0001t0002g0025others(79): Show | 99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+2109T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287253 | ||||||
chr11:36287261
|
T | C | 82 | a0001c0001t0002g0006a0001c0001t0002g0024a0001c0001t0002g0025others(79): Show | 99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+2101A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287261 | ||||||
chr11:36287265
|
G | A | 312 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(309): Show | 434 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(431): Show |
intron_variant | MODIFIER | c.51+2097C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287265 | ||||||
chr11:36287266
|
C | T | 312 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(309): Show | 434 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(431): Show |
intron_variant | MODIFIER | c.51+2096G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287266 | ||||||
chr11:36287267
|
G | A | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.51+2095C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287267 | ||||||
chr11:36287271
|
T | C | 18 | a0001c0001t0004g0041a0001c0001t0004g0042a0001c0001t0004g0196others(15): Show | 20 | HG00558.hp2 HG00621.hp1 HG01934.hp2 others(17): Show |
intron_variant | MODIFIER | c.51+2091A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287271 | ||||||
chr11:36287278
|
A | G | 16 | a0001c0001t0005g0036a0001c0001t0005g0064a0001c0001t0005g0140others(13): Show | 18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.51+2084T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287278 | ||||||
chr11:36287279
|
C | CTACATAC others(505): Show |
1 | a0001c0001t0017g0317 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.51+2082_51+2083ins others(512): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287279 | ||||||
chr11:36287280
|
T | C | 86 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0012others(83): Show | 119 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.51+2082A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287280 | ||||||
chr11:36287281
|
A | C | 2 | a0003c0003t0005g0066a0003c0003t0005g0067 | 2 | HG01109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.51+2081T>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287281 | ||||||
chr11:36287285
|
A | G | 82 | a0001c0001t0002g0006a0001c0001t0002g0024a0001c0001t0002g0025others(79): Show | 99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+2077T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287285 | ||||||
chr11:36287293
|
T | C | 82 | a0001c0001t0002g0006a0001c0001t0002g0024a0001c0001t0002g0025others(79): Show | 99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+2069A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287293 | ||||||
chr11:36287297
|
G | A | 312 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(309): Show | 434 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(431): Show |
intron_variant | MODIFIER | c.51+2065C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287297 | ||||||
chr11:36287298
|
C | T | 312 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(309): Show | 434 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(431): Show |
intron_variant | MODIFIER | c.51+2064G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287298 | ||||||
chr11:36287299
|
G | A | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.51+2063C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287299 | ||||||
chr11:36287303
|
T | C | 8 | a0001c0001t0004g0042a0001c0001t0004g0205a0001c0001t0004g0206others(5): Show | 9 | HG01934.hp2 HG01981.hp2 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.51+2059A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287303 | ||||||
chr11:36287310
|
A | G | 16 | a0001c0001t0005g0036a0001c0001t0005g0064a0001c0001t0005g0140others(13): Show | 18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.51+2052T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287310 | ||||||
chr11:36287312
|
T | C | 86 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0012others(83): Show | 119 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.51+2050A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287312 | ||||||
chr11:36287313
|
A | C | 1 | a0003c0003t0005g0066 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.51+2049T>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287313 | ||||||
chr11:36287313
|
A | CCATACTA others(1945): Show |
1 | a0003c0003t0005g0067 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.51+2049_51+2050ins others(1952): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287313 | ||||||
chr11:36287317
|
A | G | 82 | a0001c0001t0002g0006a0001c0001t0002g0024a0001c0001t0002g0025others(79): Show | 99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+2045T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287317 | ||||||
chr11:36287325
|
T | C | 82 | a0001c0001t0002g0006a0001c0001t0002g0024a0001c0001t0002g0025others(79): Show | 99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+2037A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287325 | ||||||
chr11:36287329
|
G | A | 312 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(309): Show | 434 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(431): Show |
intron_variant | MODIFIER | c.51+2033C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287329 | ||||||
chr11:36287330
|
C | T | 312 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(309): Show | 434 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(431): Show |
intron_variant | MODIFIER | c.51+2032G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287330 | ||||||
chr11:36287331
|
G | A | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.51+2031C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287331 | ||||||
chr11:36287335
|
T | C | 1 | a0001c0001t0004g0211 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.51+2027A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287335 | ||||||
chr11:36287342
|
A | G | 16 | a0001c0001t0005g0036a0001c0001t0005g0064a0001c0001t0005g0140others(13): Show | 18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.51+2020T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287342 | ||||||
chr11:36287344
|
T | C | 86 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0012others(83): Show | 119 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.51+2018A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287344 | ||||||
chr11:36287345
|
A | C | 1 | a0003c0003t0005g0066 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.51+2017T>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287345 | ||||||
chr11:36287349
|
A | G | 81 | a0001c0001t0002g0006a0001c0001t0002g0024a0001c0001t0002g0025others(78): Show | 98 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.51+2013T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287349 | ||||||
chr11:36287357
|
T | C | 82 | a0001c0001t0002g0006a0001c0001t0002g0024a0001c0001t0002g0025others(79): Show | 99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+2005A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287357 | ||||||
chr11:36287361
|
G | A | 312 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(309): Show | 434 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(431): Show |
intron_variant | MODIFIER | c.51+2001C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287361 | ||||||
chr11:36287362
|
C | T | 312 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(309): Show | 434 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(431): Show |
intron_variant | MODIFIER | c.51+2000G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287362 | ||||||
chr11:36287363
|
G | A | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.51+1999C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287363 | ||||||
chr11:36287363
|
G | GTAGTATG others(857): Show |
1 | a0001c0001t0001g0159 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.51+1998_51+1999ins others(864): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287363 | ||||||
chr11:36287367
|
T | C | 1 | a0001c0001t0002g0129 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.51+1995A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287367 | ||||||
chr11:36287374
|
A | G | 16 | a0001c0001t0005g0036a0001c0001t0005g0064a0001c0001t0005g0140others(13): Show | 18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.51+1988T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287374 | ||||||
chr11:36287376
|
T | C | 86 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0012others(83): Show | 119 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.51+1986A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287376 | ||||||
chr11:36287377
|
A | C | 1 | a0003c0003t0005g0066 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.51+1985T>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287377 | ||||||
chr11:36287381
|
A | G | 82 | a0001c0001t0002g0006a0001c0001t0002g0024a0001c0001t0002g0025others(79): Show | 99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+1981T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287381 | ||||||
chr11:36287389
|
T | C | 82 | a0001c0001t0002g0006a0001c0001t0002g0024a0001c0001t0002g0025others(79): Show | 99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+1973A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287389 | ||||||
chr11:36287393
|
G | A | 312 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(309): Show | 434 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(431): Show |
intron_variant | MODIFIER | c.51+1969C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287393 | ||||||
chr11:36287394
|
C | T | 311 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(308): Show | 432 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(429): Show |
intron_variant | MODIFIER | c.51+1968G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287394 | ||||||
chr11:36287395
|
G | A | 210 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(207): Show | 295 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.51+1967C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287395 | ||||||
chr11:36287406
|
A | G | 16 | a0001c0001t0005g0036a0001c0001t0005g0064a0001c0001t0005g0140others(13): Show | 18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.51+1956T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287406 | ||||||
chr11:36287408
|
T | C | 84 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0012others(81): Show | 117 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.51+1954A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287408 | ||||||
chr11:36287409
|
A | CCATACTA others(1497): Show |
1 | a0003c0003t0005g0066 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.51+1953_51+1954ins others(1504): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287409 | ||||||
chr11:36287413
|
A | G | 9 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0070others(6): Show | 11 | HG01891.hp2 HG02257.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.51+1949T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287413 | ||||||
chr11:36287421
|
T | C | 1 | a0001c0001t0002g0080 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.51+1941A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287421 | ||||||
chr11:36287425
|
G | A | 312 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(309): Show | 434 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(431): Show |
intron_variant | MODIFIER | c.51+1937C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287425 | ||||||
chr11:36287426
|
T | C | 4 | a0001c0001t0001g0163a0001c0001t0001g0314a0001c0001t0001g0315others(1): Show | 4 | HG01243.hp1 HG01261.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+1936A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287426 | ||||||
chr11:36287427
|
G | A | 210 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(207): Show | 295 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.51+1935C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287427 | ||||||
chr11:36287431
|
T | C | 81 | a0001c0001t0002g0006a0001c0001t0002g0024a0001c0001t0002g0025others(78): Show | 98 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.51+1931A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287431 | ||||||
chr11:36287438
|
A | G | 3 | a0001c0001t0005g0145a0001c0001t0005g0151a0001c0001t0012g0144 | 3 | HG02809.hp2 HG03041.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.51+1924T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287438 | ||||||
chr11:36287440
|
T | C | 11 | a0001c0001t0001g0005a0001c0001t0001g0063a0001c0001t0001g0303others(8): Show | 18 | HG00323.hp2 HG00642.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.51+1922A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287440 | ||||||
chr11:36287440
|
T | TACATACT others(343): Show |
1 | a0001c0001t0001g0213 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.51+1921_51+1922ins others(350): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287440 | ||||||
chr11:36287440
|
T | TACATACT others(375): Show |
1 | a0001c0001t0003g0018 | 3 | HG02559.hp2 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.51+1921_51+1922ins others(382): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287440 | ||||||
chr11:36287440
|
T | TACATACT others(1340): Show |
1 | a0001c0001t0001g0162 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.51+1921_51+1922ins others(1347): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287440 | ||||||
chr11:36287440
|
T | TACATACT others(1372): Show |
1 | a0001c0001t0001g0161 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.51+1921_51+1922ins others(1379): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287440 | ||||||
chr11:36287440
|
T | TACATACT others(2716): Show |
1 | a0001c0001t0001g0160 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.51+1921_51+1922ins others(2723): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287440 | ||||||
chr11:36287440
|
T | TACATACT others(2391): Show |
1 | a0001c0001t0001g0158 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.51+1921_51+1922ins others(2398): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287440 | ||||||
chr11:36287440
|
T | TACATACT others(1239): Show |
1 | a0001c0001t0005g0151 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.51+1921_51+1922ins others(1246): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287440 | ||||||
chr11:36287440
|
T | TACATACT others(2231): Show |
1 | a0001c0001t0012g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.51+1921_51+1922ins others(2238): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287440 | ||||||
chr11:36287441
|
C | A | 303 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(300): Show | 423 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(420): Show |
intron_variant | MODIFIER | c.51+1921G>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287441 | ||||||
chr11:36287442
|
T | C | 103 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0012others(100): Show | 140 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.51+1920A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287442 | ||||||
chr11:36287442
|
T | TAC | 4 | a0001c0001t0001g0213a0001c0001t0003g0018a0001c0001t0005g0151others(1): Show | 6 | HG02559.hp2 HG02809.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.51+1919_51+1920ins others(2): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287442 | ||||||
chr11:36287443
|
A | ACG | 4 | a0001c0001t0001g0158a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG02055.hp2 HG02717.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+1918_51+1919ins others(2): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287443 | ||||||
chr11:36287443
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.51+1919T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287443 | ||||||
chr11:36287618
|
A | T | 82 | a0001c0001t0002g0006a0001c0001t0002g0024a0001c0001t0002g0025others(79): Show | 99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+1744T>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287618 | ||||||
chr11:36287667
|
C | T | 3 | a0002c0002t0006g0077a0002c0002t0006g0078a0002c0002t0006g0079 | 3 | HG02615.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.51+1695G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287667 | ||||||
chr11:36287744
|
G | A | 16 | a0001c0001t0005g0036a0001c0001t0005g0064a0001c0001t0005g0140others(13): Show | 18 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.51+1618C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287744 | ||||||
chr11:36287913
|
T | C | 19 | a0001c0001t0003g0001a0001c0001t0003g0008a0001c0001t0003g0014others(16): Show | 43 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.51+1449A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36287913 | ||||||
chr11:36288083
|
A | G | 1 | a0001c0001t0001g0224 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.51+1279T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36288083 | ||||||
chr11:36288178
|
A | G | 317 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(314): Show | 444 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(441): Show |
intron_variant | MODIFIER | c.51+1184T>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36288178 | ||||||
chr11:36288194
|
T | G | 2 | a0001c0001t0001g0157a0001c0001t0001g0183 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.51+1168A>C | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36288194 | ||||||
chr11:36288195
|
G | A | 3 | a0001c0001t0001g0314a0001c0001t0001g0315a0001c0001t0001g0316 | 3 | HG01243.hp1 HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.51+1167C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36288195 | ||||||
chr11:36288356
|
G | GT | 11 | a0001c0001t0001g0186a0001c0001t0002g0130a0001c0001t0002g0132others(8): Show | 11 | HG01123.hp1 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.51+1005dupA | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36288356 | ||||||
chr11:36288359
|
T | TA | 37 | a0001c0001t0001g0019a0001c0001t0001g0047a0001c0001t0001g0048others(34): Show | 46 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.51+1002dupT | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36288359 | ||||||
chr11:36288359
|
T | TTA | 23 | a0001c0001t0001g0213a0001c0001t0002g0035a0001c0001t0003g0001others(20): Show | 50 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.51+1002_51+1003ins others(2): Show |
COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36288359 | ||||||
chr11:36288360
|
A | T | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.51+1002T>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36288360 | ||||||
chr11:36288361
|
A | T | 8 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0005g0036others(5): Show | 9 | HG02735.hp1 HG02738.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.51+1001T>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36288361 | ||||||
chr11:36288374
|
AG | A | 31 | a0001c0001t0001g0054a0001c0001t0001g0068a0001c0001t0001g0156others(28): Show | 35 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.51+987delC | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36288374 | ||||||
chr11:36288375
|
G | A | 284 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(281): Show | 406 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(403): Show |
intron_variant | MODIFIER | c.51+987C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36288375 | ||||||
chr11:36288379
|
G | A | 1 | a0001c0001t0001g0023 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.51+983C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36288379 | ||||||
chr11:36288539
|
A | C | 99 | a0001c0001t0001g0152a0001c0001t0002g0006a0001c0001t0002g0024others(96): Show | 118 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.51+823T>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36288539 | ||||||
chr11:36288694
|
G | C | 81 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0012others(78): Show | 113 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.51+668C>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36288694 | ||||||
chr11:36288726
|
G | C | 1 | a0001c0001t0005g0064 | 2 | HG00438.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.51+636C>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36288726 | ||||||
chr11:36288733
|
G | GA | 3 | a0001c0001t0001g0314a0001c0001t0001g0315a0001c0001t0001g0316 | 3 | HG01243.hp1 HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.51+628dupT | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36288733 | ||||||
chr11:36288949
|
T | C | 1 | a0001c0001t0001g0065 | 2 | NA18975.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.51+413A>G | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36288949 | ||||||
chr11:36288951
|
G | A | 1 | a0001c0001t0017g0317 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.51+411C>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36288951 | ||||||
chr11:36288983
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.51+379G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36288983 | ||||||
chr11:36289127
|
C | T | 82 | a0001c0001t0002g0006a0001c0001t0002g0024a0001c0001t0002g0025others(79): Show | 99 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.51+235G>A | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36289127 | ||||||
chr11:36289307
|
C | A | 3 | a0001c0001t0003g0014a0001c0001t0003g0318a0001c0001t0003g0319 | 6 | HG00621.hp2 NA18942.hp1 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.51+55G>T | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36289307 | ||||||
chr11:36289347
|
A | AC | 3 | a0001c0001t0001g0023a0001c0001t0001g0068a0001c0001t0001g0069 | 4 | HG01123.hp2 HG01515.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+14dupG | COMMD9 | ENSG00000110442.12 | transcript | ENST00000263401.10 | protein_coding | 1/5 | chr11 | 36289347 |