geneid | 149951 |
---|---|
ensemblid | ENSG00000149600.12 |
hgncid | 16223 |
symbol | COMMD7 |
name | COMM domain containing 7 |
refseq_nuc | NM_053041.3 |
refseq_prot | NP_444269.2 |
ensembl_nuc | ENST00000278980.11 |
ensembl_prot | ENSP00000278980.6 |
mane_status | MANE Select |
chr | chr20 |
start | 32702699 |
end | 32743467 |
strand | - |
ver | v1.2 |
region | chr20:32702699-32743467 |
region5000 | chr20:32697699-32748467 |
regionname0 | COMMD7_chr20_32702699_32743467 |
regionname5000 | COMMD7_chr20_32697699_32748467 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 200 | 399 | 90 | 76 | 171 | 16 | 44 | 132 | COMMD7_chr20_32697699_32748467 | COMMD7 | copy fasta | chr20 | 32697699 | 32748467 |
a0002 | 0/0 | 190 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | copy fasta | chr20 | 32697699 | 32748467 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 760 | 218 | 48 | 37 | 91 | 13 | 28 | COMMD7_chr20_32697699_32748467 | COMMD7 | copy fasta | chr20 | 32697699 | 32748467 |
t0002 | 1/0 | 760 | 168 | 31 | 38 | 80 | 3 | 15 | COMMD7_chr20_32697699_32748467 | COMMD7 | copy fasta | chr20 | 32697699 | 32748467 |
t0003 | 0/0 | 759 | 5 | 5 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | copy fasta | chr20 | 32697699 | 32748467 |
t0004 | 0/0 | 759 | 4 | 4 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | copy fasta | chr20 | 32697699 | 32748467 |
t0005 | 0/0 | 760 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | copy fasta | chr20 | 32697699 | 32748467 |
t0006 | 0/0 | 760 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | copy fasta | chr20 | 32697699 | 32748467 |
t0007 | 0/0 | 760 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | copy fasta | chr20 | 32697699 | 32748467 |
t0008 | 0/0 | 760 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | copy fasta | chr20 | 32697699 | 32748467 |
t0009 | 0/0 | 760 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | copy fasta | chr20 | 32697699 | 32748467 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0010 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0013 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0018 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0367 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 603 | 399 | 90 | 76 | 171 | 16 | 44 | COMMD7_chr20_32697699_32748467 | COMMD7 | copy fasta | chr20 | 32697699 | 32748467 |
a0002c0002 | 0/0 | 603 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | copy fasta | chr20 | 32697699 | 32748467 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 1362 | 217 | 48 | 37 | 90 | 13 | 28 | COMMD7_chr20_32697699_32748467 | COMMD7 | copy fasta | chr20 | 32697699 | 32748467 |
a0001c0001t0002 | 1/0 | 1362 | 168 | 31 | 38 | 80 | 3 | 15 | COMMD7_chr20_32697699_32748467 | COMMD7 | copy fasta | chr20 | 32697699 | 32748467 |
a0001c0001t0003 | 0/0 | 1361 | 5 | 5 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | copy fasta | chr20 | 32697699 | 32748467 |
a0001c0001t0004 | 0/0 | 1361 | 4 | 4 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | copy fasta | chr20 | 32697699 | 32748467 |
a0001c0001t0005 | 0/0 | 1362 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | copy fasta | chr20 | 32697699 | 32748467 |
a0001c0001t0006 | 0/0 | 1362 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | copy fasta | chr20 | 32697699 | 32748467 |
a0001c0001t0007 | 0/0 | 1362 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | copy fasta | chr20 | 32697699 | 32748467 |
a0001c0001t0008 | 0/0 | 1362 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | copy fasta | chr20 | 32697699 | 32748467 |
a0001c0001t0009 | 0/0 | 1362 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | copy fasta | chr20 | 32697699 | 32748467 |
a0002c0002t0001 | 0/0 | 1362 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | copy fasta | chr20 | 32697699 | 32748467 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0010 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0018 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0002g0367 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0003g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0003g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0003g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0003g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0004g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0004g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0004g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0005g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0006g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0007g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0008g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0001c0001t0009g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0112 | EUR | GBR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | GBR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0190 | EUR | GBR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0322 | EUR | GBR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0319 | EUR | FIN | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0336 | EUR | FIN | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0173 | EUR | FIN | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0082 | EUR | FIN | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | CHS | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | CHS | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | CHS | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | CHS | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | CHS | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0077 | EAS | CHS | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | CHS | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | CHS | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | CHS | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0349 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0111 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0229 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0181 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00741 | hp1 | a0001 | c0001 | t0009 | g0287 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0371 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0356 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0317 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0161 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0342 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0338 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0350 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0256 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0157 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0156 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0185 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0323 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0348 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0346 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0213 | AMR | CLM | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0351 | AMR | CLM | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0178 | AMR | CLM | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0315 | AMR | CLM | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0186 | AMR | CLM | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0370 | AMR | CLM | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | CLM | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0330 | AMR | CLM | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0215 | AMR | CLM | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0182 | AMR | CLM | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | CLM | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | CLM | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0329 | AMR | CLM | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | CLM | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | CLM | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0328 | AMR | CLM | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0069 | EUR | IBS | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0067 | EUR | IBS | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0339 | EUR | IBS | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0343 | EUR | IBS | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0071 | EUR | IBS | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | ACB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0361 | AFR | ACB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0262 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0227 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0283 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0331 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0226 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | KHV | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | KHV | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0254 | AFR | ACB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0289 | AFR | ACB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | KHV | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | KHV | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | KHV | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | KHV | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | KHV | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | KHV | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | KHV | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | KHV | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | KHV | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | KHV | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | KHV | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0372 | EAS | KHV | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | ACB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | ACB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0333 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | CDX | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | CDX | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | CDX | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0334 | AFR | ACB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0180 | AFR | ACB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0224 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0195 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | ACB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0151 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0187 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0320 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0214 | AMR | PEL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | ACB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0365 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0284 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0352 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0240 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0360 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0294 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0363 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0355 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0167 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0362 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0337 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0264 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0300 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0293 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0335 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0244 | AFR | ESN | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | ESN | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0292 | AFR | ESN | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0123 | AFR | ESN | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0176 | AFR | ESN | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0118 | AFR | ESN | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03041 | hp2 | a0001 | c0001 | t0004 | g0291 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0114 | AFR | MSL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0285 | AFR | MSL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0159 | AFR | ESN | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ESN | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | ESN | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | ESN | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | MSL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | MSL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | MSL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0318 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0198 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | MSL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | MSL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0172 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0326 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0196 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0344 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0364 | AFR | ESN | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03516 | hp2 | a0001 | c0001 | t0006 | g0120 | AFR | ESN | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0255 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0104 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0354 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0203 | SAS | STU | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | STU | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0353 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0345 | SAS | PJL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0347 | SAS | BEB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0265 | SAS | BEB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0252 | SAS | BEB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0188 | SAS | BEB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | STU | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0327 | SAS | STU | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0242 | SAS | STU | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | STU | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | STU | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0358 | SAS | STU | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0314 | SAS | STU | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG04228 | hp2 | a0001 | c0001 | t0008 | g0245 | SAS | STU | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0359 | AFR | YRI | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0369 | AFR | YRI | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | CHB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | YRI | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | YRI | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0357 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0295 | AFR | LWK | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0219 | AFR | LWK | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | LWK | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19091 | hp2 | a0001 | c0001 | t0007 | g0199 | EAS | JPT | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0296 | AFR | YRI | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | YRI | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ASW | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ASW | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | TSI | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0332 | EUR | TSI | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | GIH | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0105 | SAS | GIH | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0341 | AMR | CLM | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0366 | AFR | ACB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0340 | AFR | ACB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0290 | AFR | ACB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0288 | AFR | MSL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0115 | AFR | MSL | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0205 | AFR | USA | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | USA | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0368 | AFR | LWK | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | LWK | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0018 | REF | REF | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0367 | REF | REF | COMMD7_chr20_32697699_32748467 | COMMD7 | chr20 | 32697699 | 32748467 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:32703414
|
G | A | 1 | a0002 | 1 | HG00558.hp2 | stop_gained | HIGH | c.571C>T | p.Arg191* | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 9/9 | 647/1362 | 571/603 | 191/200 | chr20 | 32703414 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:32702754
|
C | G | 1 | a0001c0001t0006 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*628G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 9/9 | 628 | chr20 | 32702754 | |||||
chr20:32703003
|
G | T | 1 | a0001c0001t0008 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*379C>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 9/9 | 379 | chr20 | 32703003 | |||||
chr20:32703060
|
C | G | 1 | a0001c0001t0005 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*322G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 9/9 | 322 | chr20 | 32703060 | |||||
chr20:32703114
|
G | A | 1 | a0001c0001t0004 | 4 | HG02630.hp1 HG02886.hp1 HG02970.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*268C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 9/9 | 268 | chr20 | 32703114 | |||||
chr20:32703135
|
TA | T | 2 | a0001c0001t0003a0001c0001t0004 | 9 | HG02280.hp1 HG02630.hp1 HG02886.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*246delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 9/9 | 246 | chr20 | 32703135 | |||||
chr20:32703178
|
A | G | 1 | a0001c0001t0007 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*204T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 9/9 | 204 | chr20 | 32703178 | |||||
chr20:32703354
|
G | A | 1 | a0001c0001t0009 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*28C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 9/9 | 28 | chr20 | 32703354 | |||||
chr20:32703359
|
C | T | 4 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(1): Show | 220 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*23G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 9/9 | 23 | chr20 | 32703359 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:32703625
|
A | T | 1 | a0001c0001t0002g0078 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.527-167T>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 8/8 | chr20 | 32703625 | ||||||
chr20:32703681
|
C | A | 176 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.527-223G>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 8/8 | chr20 | 32703681 | ||||||
chr20:32703738
|
G | C | 1 | a0001c0001t0002g0154 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.527-280C>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 8/8 | chr20 | 32703738 | ||||||
chr20:32703796
|
C | T | 1 | a0001c0001t0001g0363 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.526+227G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 8/8 | chr20 | 32703796 | ||||||
chr20:32703823
|
A | G | 74 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(71): Show | 78 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(75): Show |
intron_variant | MODIFIER | c.526+200T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 8/8 | chr20 | 32703823 | ||||||
chr20:32703939
|
C | T | 2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | NA18953.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.526+84G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 8/8 | chr20 | 32703939 | ||||||
chr20:32704020
|
C | T | 10 | a0001c0001t0001g0109a0001c0001t0003g0007a0001c0001t0003g0295others(7): Show | 11 | HG01109.hp2 HG02280.hp1 HG02630.hp1 others(8): Show |
splice_region_variant&intron_variant | LOW | c.526+3G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 8/8 | chr20 | 32704020 | ||||||
chr20:32704117
|
GGGCA | G | 71 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(68): Show | 74 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.478-50_478-47delTG others(2): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 7/8 | chr20 | 32704117 | ||||||
chr20:32704178
|
G | A | 1 | a0001c0001t0005g0359 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.478-107C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 7/8 | chr20 | 32704178 | ||||||
chr20:32704240
|
C | T | 8 | a0001c0001t0002g0063a0001c0001t0002g0160a0001c0001t0002g0161others(5): Show | 8 | HG01070.hp2 NA18944.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-169G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 7/8 | chr20 | 32704240 | ||||||
chr20:32704241
|
G | A | 1 | a0001c0001t0001g0333 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.478-170C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 7/8 | chr20 | 32704241 | ||||||
chr20:32704286
|
G | A | 3 | a0001c0001t0002g0231a0001c0001t0002g0232a0001c0001t0002g0233 | 3 | HG02129.hp1 NA18964.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.477+154C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 7/8 | chr20 | 32704286 | ||||||
chr20:32704342
|
G | T | 1 | a0001c0001t0005g0359 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.477+98C>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 7/8 | chr20 | 32704342 | ||||||
chr20:32704382
|
T | TATG | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 232 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.477+57_477+58insCA others(1): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 7/8 | chr20 | 32704382 | ||||||
chr20:32704496
|
CA | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(171): Show | 190 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(187): Show |
splice_region_variant&intron_variant | LOW | c.428-8delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 6/8 | chr20 | 32704496 | ||||||
chr20:32704496
|
CAA | C | 29 | a0001c0001t0001g0003a0001c0001t0001g0041a0001c0001t0001g0042others(26): Show | 32 | HG02040.hp2 HG02056.hp2 HG02280.hp1 others(29): Show |
splice_region_variant&intron_variant | LOW | c.428-9_428-8delTT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 6/8 | chr20 | 32704496 | ||||||
chr20:32704496
|
CAAA | C | 9 | a0001c0001t0001g0109a0001c0001t0003g0295a0001c0001t0003g0296others(6): Show | 9 | HG01109.hp2 HG02630.hp1 HG02886.hp1 others(6): Show |
splice_region_variant&intron_variant | LOW | c.428-10_428-8delTTT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 6/8 | chr20 | 32704496 | ||||||
chr20:32704510
|
A | G | 1 | a0001c0001t0003g0007 | 2 | HG02280.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.428-21T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 6/8 | chr20 | 32704510 | ||||||
chr20:32704701
|
G | T | 10 | a0001c0001t0001g0109a0001c0001t0003g0007a0001c0001t0003g0295others(7): Show | 11 | HG01109.hp2 HG02280.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.427+113C>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 6/8 | chr20 | 32704701 | ||||||
chr20:32704992
|
G | A | 7 | a0001c0001t0003g0295a0001c0001t0003g0296a0001c0001t0003g0369others(4): Show | 7 | HG02630.hp1 HG02886.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.337-88C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32704992 | ||||||
chr20:32704996
|
CAGATAGT others(14): Show |
C | 1 | a0001c0001t0002g0118 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.337-113_337-93delT others(20): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32704996 | ||||||
chr20:32705031
|
G | A | 10 | a0001c0001t0001g0109a0001c0001t0003g0007a0001c0001t0003g0295others(7): Show | 11 | HG01109.hp2 HG02280.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.337-127C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705031 | ||||||
chr20:32705075
|
G | T | 1 | a0001c0001t0001g0117 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.337-171C>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705075 | ||||||
chr20:32705312
|
G | GTATATAT others(15): Show |
10 | a0001c0001t0001g0109a0001c0001t0003g0007a0001c0001t0003g0295others(7): Show | 11 | HG01109.hp2 HG02280.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.337-409_337-408ins others(22): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705312 | ||||||
chr20:32705316
|
A | G | 10 | a0001c0001t0001g0109a0001c0001t0003g0007a0001c0001t0003g0295others(7): Show | 11 | HG01109.hp2 HG02280.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.337-412T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705316 | ||||||
chr20:32705338
|
G | GTA | 13 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0168others(10): Show | 13 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.337-436_337-435dup others(2): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705338 | ||||||
chr20:32705348
|
A | G | 3 | a0001c0001t0001g0001a0001c0001t0001g0093a0001c0001t0001g0273 | 7 | HG00408.hp1 HG00544.hp1 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.337-444T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705348 | ||||||
chr20:32705350
|
G | A | 7 | a0001c0001t0001g0064a0001c0001t0001g0076a0001c0001t0001g0080others(4): Show | 7 | NA18947.hp1 NA18983.hp1 NA18987.hp1 others(4): Show |
intron_variant | MODIFIER | c.337-446C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705350 | ||||||
chr20:32705358
|
G | A | 8 | a0001c0001t0003g0007a0001c0001t0003g0295a0001c0001t0003g0296others(5): Show | 9 | HG02280.hp1 HG02630.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.337-454C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705358 | ||||||
chr20:32705358
|
G | GTATATAT others(15): Show |
1 | a0001c0001t0001g0109 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.337-455_337-454ins others(22): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705358 | ||||||
chr20:32705358
|
GTA | G | 38 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0025others(35): Show | 40 | HG01346.hp1 HG01358.hp2 HG01884.hp2 others(37): Show |
intron_variant | MODIFIER | c.337-456_337-455del others(2): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705358 | ||||||
chr20:32705360
|
A | G | 29 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(26): Show | 34 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(31): Show |
intron_variant | MODIFIER | c.337-456T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705360 | ||||||
chr20:32705369
|
TATATATA | T | 7 | a0001c0001t0003g0295a0001c0001t0003g0296a0001c0001t0003g0369others(4): Show | 7 | HG02630.hp1 HG02886.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.337-472_337-466del others(7): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705369 | ||||||
chr20:32705371
|
TA | T | 4 | a0001c0001t0001g0110a0001c0001t0001g0332a0001c0001t0001g0333others(1): Show | 4 | HG01258.hp2 HG02148.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.337-468delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705371 | ||||||
chr20:32705372
|
A | T | 1 | a0001c0001t0002g0256 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.337-468T>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705372 | ||||||
chr20:32705373
|
TA | T | 26 | a0001c0001t0001g0019a0001c0001t0001g0033a0001c0001t0001g0092others(23): Show | 27 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.337-470delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705373 | ||||||
chr20:32705374
|
A | T | 10 | a0001c0001t0001g0110a0001c0001t0001g0330a0001c0001t0001g0331others(7): Show | 10 | HG01109.hp1 HG01258.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.337-470T>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705374 | ||||||
chr20:32705374
|
ATAT | A | 6 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0121others(3): Show | 9 | HG02451.hp1 HG02809.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.337-473_337-471del others(3): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705374 | ||||||
chr20:32705375
|
TA | T | 6 | a0001c0001t0001g0090a0001c0001t0001g0301a0001c0001t0001g0305others(3): Show | 6 | HG01496.hp2 HG01934.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.337-472delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705375 | ||||||
chr20:32705376
|
A | AT | 6 | a0001c0001t0002g0034a0001c0001t0002g0176a0001c0001t0002g0224others(3): Show | 6 | HG02055.hp2 HG02109.hp1 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.337-473dupA | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705376 | ||||||
chr20:32705376
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0006g0120 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.337-473_337-472ins others(18): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705376 | ||||||
chr20:32705376
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0003g0007 | 2 | HG02280.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.337-473_337-472ins others(14): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705376 | ||||||
chr20:32705376
|
A | T | 85 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(82): Show | 91 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.337-472T>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705376 | ||||||
chr20:32705376
|
AT | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(106): Show | 121 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.337-473delA | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705376 | ||||||
chr20:32705377
|
T | TA | 9 | a0001c0001t0001g0064a0001c0001t0001g0076a0001c0001t0001g0080others(6): Show | 9 | HG02572.hp2 NA18947.hp1 NA18967.hp2 others(6): Show |
intron_variant | MODIFIER | c.337-474_337-473ins others(1): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705377 | ||||||
chr20:32705378
|
T | A | 6 | a0001c0001t0002g0178a0001c0001t0002g0186a0001c0001t0002g0193others(3): Show | 6 | HG01256.hp1 HG01258.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.337-474A>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705378 | ||||||
chr20:32705379
|
T | A | 4 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0276others(1): Show | 4 | HG02056.hp2 HG02145.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.337-475A>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705379 | ||||||
chr20:32705448
|
G | A | 1 | a0001c0001t0002g0197 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.337-544C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705448 | ||||||
chr20:32705518
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.337-614G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705518 | ||||||
chr20:32705531
|
G | A | 10 | a0001c0001t0001g0109a0001c0001t0003g0007a0001c0001t0003g0295others(7): Show | 11 | HG01109.hp2 HG02280.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.337-627C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705531 | ||||||
chr20:32705563
|
T | C | 1 | a0001c0001t0001g0144 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.337-659A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705563 | ||||||
chr20:32705591
|
T | C | 26 | a0001c0001t0001g0003a0001c0001t0001g0041a0001c0001t0001g0042others(23): Show | 28 | HG02040.hp2 HG02056.hp2 NA18942.hp2 others(25): Show |
intron_variant | MODIFIER | c.337-687A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705591 | ||||||
chr20:32705594
|
C | T | 60 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0035others(57): Show | 65 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.337-690G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705594 | ||||||
chr20:32705703
|
T | C | 10 | a0001c0001t0001g0109a0001c0001t0003g0007a0001c0001t0003g0295others(7): Show | 11 | HG01109.hp2 HG02280.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.337-799A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705703 | ||||||
chr20:32705714
|
A | G | 10 | a0001c0001t0001g0109a0001c0001t0003g0007a0001c0001t0003g0295others(7): Show | 11 | HG01109.hp2 HG02280.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.337-810T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705714 | ||||||
chr20:32705833
|
C | T | 2 | a0001c0001t0001g0297a0001c0001t0001g0298 | 2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.336+750G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32705833 | ||||||
chr20:32706027
|
C | T | 10 | a0001c0001t0001g0109a0001c0001t0003g0007a0001c0001t0003g0295others(7): Show | 11 | HG01109.hp2 HG02280.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.336+556G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32706027 | ||||||
chr20:32706135
|
T | C | 4 | a0001c0001t0001g0025a0001c0001t0001g0277a0001c0001t0001g0278others(1): Show | 4 | HG01891.hp2 HG02145.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.336+448A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32706135 | ||||||
chr20:32706138
|
C | T | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | HG02486.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.336+445G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32706138 | ||||||
chr20:32706161
|
G | A | 10 | a0001c0001t0001g0109a0001c0001t0003g0007a0001c0001t0003g0295others(7): Show | 11 | HG01109.hp2 HG02280.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.336+422C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32706161 | ||||||
chr20:32706198
|
CA | C | 18 | a0001c0001t0001g0003a0001c0001t0001g0041a0001c0001t0001g0042others(15): Show | 20 | HG02080.hp2 HG02273.hp2 HG03491.hp1 others(17): Show |
intron_variant | MODIFIER | c.336+384delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32706198 | ||||||
chr20:32706253
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.336+330G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32706253 | ||||||
chr20:32706294
|
A | G | 4 | a0001c0001t0001g0025a0001c0001t0001g0277a0001c0001t0001g0278others(1): Show | 4 | HG01891.hp2 HG02145.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.336+289T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32706294 | ||||||
chr20:32706414
|
G | A | 1 | a0001c0001t0005g0359 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.336+169C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32706414 | ||||||
chr20:32706512
|
C | CA | 14 | a0001c0001t0001g0109a0001c0001t0001g0129a0001c0001t0001g0130others(11): Show | 15 | HG01109.hp2 HG02280.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.336+70dupT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 5/8 | chr20 | 32706512 | ||||||
chr20:32706688
|
C | T | 14 | a0001c0001t0001g0109a0001c0001t0001g0116a0001c0001t0001g0133others(11): Show | 15 | HG01109.hp2 HG02280.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.298+16G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 4/8 | chr20 | 32706688 | ||||||
chr20:32706853
|
A | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(197): Show | 218 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.242-93T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32706853 | ||||||
chr20:32706888
|
A | C | 14 | a0001c0001t0001g0109a0001c0001t0001g0116a0001c0001t0001g0133others(11): Show | 15 | HG01109.hp2 HG02280.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.242-128T>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32706888 | ||||||
chr20:32706978
|
A | G | 103 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(100): Show | 110 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.242-218T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32706978 | ||||||
chr20:32707045
|
A | G | 2 | a0001c0001t0002g0198a0001c0001t0002g0215 | 2 | HG01346.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.242-285T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707045 | ||||||
chr20:32707069
|
C | T | 6 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0121others(3): Show | 9 | HG02451.hp1 HG02809.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.242-309G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707069 | ||||||
chr20:32707070
|
G | A | 62 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(59): Show | 65 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.242-310C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707070 | ||||||
chr20:32707117
|
C | CA | 8 | a0001c0001t0001g0109a0001c0001t0002g0171a0001c0001t0002g0202others(5): Show | 8 | HG00438.hp2 HG01109.hp2 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.242-358dupT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707117 | ||||||
chr20:32707117
|
CA | C | 144 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(141): Show | 158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.242-358delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707117 | ||||||
chr20:32707117
|
CAA | C | 61 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0035others(58): Show | 66 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.242-359_242-358del others(2): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707117 | ||||||
chr20:32707210
|
G | A | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(16): Show | 24 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(21): Show |
intron_variant | MODIFIER | c.242-450C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707210 | ||||||
chr20:32707263
|
A | G | 10 | a0001c0001t0001g0109a0001c0001t0003g0007a0001c0001t0003g0295others(7): Show | 11 | HG01109.hp2 HG02280.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.242-503T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707263 | ||||||
chr20:32707288
|
A | AATAT | 18 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(15): Show | 23 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(20): Show |
intron_variant | MODIFIER | c.242-529_242-528ins others(4): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707288 | ||||||
chr20:32707290
|
A | T | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(16): Show | 24 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(21): Show |
intron_variant | MODIFIER | c.242-530T>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707290 | ||||||
chr20:32707292
|
A | AAT | 50 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0033others(47): Show | 52 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.242-533_242-532ins others(2): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707292 | ||||||
chr20:32707292
|
A | T | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(16): Show | 24 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(21): Show |
intron_variant | MODIFIER | c.242-532T>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707292 | ||||||
chr20:32707294
|
A | T | 164 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(161): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.242-534T>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707294 | ||||||
chr20:32707296
|
T | A | 5 | a0001c0001t0001g0045a0001c0001t0001g0050a0001c0001t0003g0295others(2): Show | 5 | NA18522.hp2 NA18961.hp2 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.242-536A>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707296 | ||||||
chr20:32707322
|
T | A | 9 | a0001c0001t0001g0119a0001c0001t0001g0129a0001c0001t0001g0130others(6): Show | 9 | HG01891.hp1 HG02572.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.242-562A>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707322 | ||||||
chr20:32707324
|
T | C | 2 | a0001c0001t0001g0106a0001c0001t0001g0108 | 2 | HG03017.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.242-564A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707324 | ||||||
chr20:32707380
|
C | T | 1 | a0001c0001t0002g0208 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.242-620G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707380 | ||||||
chr20:32707502
|
TAG | T | 6 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0121others(3): Show | 9 | HG02451.hp1 HG02809.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.242-744_242-743del others(2): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707502 | ||||||
chr20:32707531
|
G | C | 2 | a0001c0001t0001g0109a0001c0001t0006g0120 | 2 | HG01109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.242-771C>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707531 | ||||||
chr20:32707564
|
C | T | 1 | a0001c0001t0001g0299 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.242-804G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707564 | ||||||
chr20:32707639
|
T | C | 1 | a0001c0001t0005g0359 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.242-879A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707639 | ||||||
chr20:32707824
|
A | G | 1 | a0001c0001t0001g0330 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.242-1064T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707824 | ||||||
chr20:32707832
|
A | G | 1 | a0001c0001t0002g0216 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.242-1072T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32707832 | ||||||
chr20:32708042
|
A | G | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 233 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.242-1282T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32708042 | ||||||
chr20:32708498
|
C | T | 4 | a0001c0001t0001g0124a0001c0001t0001g0308a0001c0001t0001g0309others(1): Show | 4 | NA18942.hp2 NA18949.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.242-1738G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32708498 | ||||||
chr20:32708577
|
T | C | 1 | a0001c0001t0001g0320 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.242-1817A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32708577 | ||||||
chr20:32708656
|
C | CTT | 16 | a0001c0001t0001g0066a0001c0001t0001g0082a0001c0001t0001g0109others(13): Show | 17 | HG00323.hp2 HG01070.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.242-1898_242-1897d others(4): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32708656 | ||||||
chr20:32708656
|
C | CTTT | 179 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(176): Show | 197 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.242-1899_242-1897d others(5): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32708656 | ||||||
chr20:32708656
|
C | CTTTT | 12 | a0001c0001t0001g0036a0001c0001t0001g0089a0001c0001t0001g0119others(9): Show | 12 | HG02056.hp1 HG02148.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.242-1900_242-1897d others(6): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32708656 | ||||||
chr20:32708735
|
C | T | 1 | a0001c0001t0002g0240 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.242-1975G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32708735 | ||||||
chr20:32709164
|
G | A | 1 | a0001c0001t0002g0111 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.242-2404C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32709164 | ||||||
chr20:32709196
|
G | A | 26 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(23): Show | 34 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(31): Show |
intron_variant | MODIFIER | c.242-2436C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32709196 | ||||||
chr20:32709285
|
A | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0121others(3): Show | 9 | HG02451.hp1 HG02809.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.242-2525T>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32709285 | ||||||
chr20:32709291
|
C | T | 2 | a0001c0001t0001g0129a0001c0001t0001g0130 | 2 | HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.242-2531G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32709291 | ||||||
chr20:32709307
|
C | T | 13 | a0001c0001t0002g0104a0001c0001t0002g0172a0001c0001t0002g0173others(10): Show | 13 | HG00323.hp1 HG01106.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.242-2547G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32709307 | ||||||
chr20:32709399
|
C | CA | 22 | a0001c0001t0002g0015a0001c0001t0002g0031a0001c0001t0002g0063others(19): Show | 23 | HG00673.hp1 HG01175.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.242-2640dupT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32709399 | ||||||
chr20:32709399
|
CA | C | 18 | a0001c0001t0001g0071a0001c0001t0001g0097a0001c0001t0001g0101others(15): Show | 18 | HG00438.hp1 HG01109.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.242-2640delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32709399 | ||||||
chr20:32709399
|
CAA | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(191): Show | 212 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.242-2641_242-2640d others(4): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32709399 | ||||||
chr20:32709455
|
G | C | 2 | a0001c0001t0001g0109a0001c0001t0006g0120 | 2 | HG01109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.242-2695C>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32709455 | ||||||
chr20:32709478
|
C | G | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 233 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.242-2718G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32709478 | ||||||
chr20:32709634
|
C | T | 71 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(68): Show | 74 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.242-2874G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32709634 | ||||||
chr20:32709766
|
G | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 232 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.242-3006C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32709766 | ||||||
chr20:32709807
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.242-3047G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32709807 | ||||||
chr20:32709947
|
C | T | 1 | a0001c0001t0002g0210 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.242-3187G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32709947 | ||||||
chr20:32709986
|
C | T | 98 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(95): Show | 105 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.242-3226G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32709986 | ||||||
chr20:32710057
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.242-3297A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32710057 | ||||||
chr20:32710070
|
A | G | 8 | a0001c0001t0003g0007a0001c0001t0003g0295a0001c0001t0003g0296others(5): Show | 9 | HG02280.hp1 HG02630.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.242-3310T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32710070 | ||||||
chr20:32710102
|
G | A | 1 | a0001c0001t0002g0183 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.242-3342C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32710102 | ||||||
chr20:32710213
|
G | A | 2 | a0001c0001t0001g0068a0001c0001t0001g0075 | 2 | NA18960.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.242-3453C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32710213 | ||||||
chr20:32710474
|
G | A | 1 | a0001c0001t0002g0191 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.242-3714C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32710474 | ||||||
chr20:32710515
|
G | C | 199 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(196): Show | 217 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.242-3755C>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32710515 | ||||||
chr20:32710632
|
G | T | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 232 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.242-3872C>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32710632 | ||||||
chr20:32710695
|
C | T | 2 | a0001c0001t0001g0311a0001c0001t0001g0313 | 2 | NA18970.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.242-3935G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32710695 | ||||||
chr20:32710728
|
CA | C | 6 | a0001c0001t0001g0133a0001c0001t0002g0157a0001c0001t0002g0177others(3): Show | 6 | HG00558.hp1 HG01167.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.242-3969delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32710728 | ||||||
chr20:32710728
|
CAA | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 152 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.242-3970_242-3969d others(4): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32710728 | ||||||
chr20:32710733
|
A | AC | 71 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(68): Show | 74 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.242-3974_242-3973i others(3): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32710733 | ||||||
chr20:32711057
|
G | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(135): Show | 154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.242-4297C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32711057 | ||||||
chr20:32711132
|
C | T | 4 | a0001c0001t0001g0116a0001c0001t0001g0133a0001c0001t0001g0134others(1): Show | 4 | HG02486.hp2 HG02965.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.242-4372G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32711132 | ||||||
chr20:32711139
|
A | G | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 232 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.242-4379T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32711139 | ||||||
chr20:32711167
|
C | T | 3 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0276 | 3 | HG02145.hp1 HG03139.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.242-4407G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32711167 | ||||||
chr20:32711184
|
G | A | 1 | a0001c0001t0002g0112 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.242-4424C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32711184 | ||||||
chr20:32711258
|
G | A | 1 | a0001c0001t0005g0359 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.242-4498C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32711258 | ||||||
chr20:32711259
|
T | C | 1 | a0001c0001t0002g0253 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.242-4499A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32711259 | ||||||
chr20:32711376
|
G | A | 2 | a0001c0001t0001g0273a0001c0001t0002g0283 | 2 | HG00408.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.242-4616C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32711376 | ||||||
chr20:32711378
|
C | T | 1 | a0001c0001t0001g0312 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.242-4618G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32711378 | ||||||
chr20:32711380
|
G | C | 5 | a0001c0001t0001g0025a0001c0001t0001g0277a0001c0001t0001g0278others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.242-4620C>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32711380 | ||||||
chr20:32711407
|
A | AT | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 231 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.242-4648dupA | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32711407 | ||||||
chr20:32711415
|
T | TA | 7 | a0001c0001t0001g0051a0001c0001t0001g0060a0001c0001t0001g0140others(4): Show | 7 | HG00438.hp1 HG02602.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.242-4656dupT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32711415 | ||||||
chr20:32711716
|
T | A | 1 | a0001c0001t0005g0359 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.242-4956A>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32711716 | ||||||
chr20:32711795
|
T | C | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 232 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.242-5035A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32711795 | ||||||
chr20:32711921
|
G | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 232 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.242-5161C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32711921 | ||||||
chr20:32711950
|
C | T | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 232 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.242-5190G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32711950 | ||||||
chr20:32711951
|
G | A | 1 | a0001c0001t0002g0283 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.242-5191C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32711951 | ||||||
chr20:32711962
|
A | T | 97 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(94): Show | 104 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.242-5202T>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32711962 | ||||||
chr20:32712014
|
GT | G | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 232 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.242-5255delA | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712014 | ||||||
chr20:32712037
|
C | T | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(16): Show | 24 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(21): Show |
intron_variant | MODIFIER | c.242-5277G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712037 | ||||||
chr20:32712120
|
A | C | 2 | a0001c0001t0001g0109a0001c0001t0006g0120 | 2 | HG01109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.242-5360T>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712120 | ||||||
chr20:32712218
|
C | T | 1 | a0001c0001t0002g0219 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.242-5458G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712218 | ||||||
chr20:32712251
|
C | A | 62 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(59): Show | 65 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.242-5491G>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712251 | ||||||
chr20:32712267
|
C | T | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 232 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.242-5507G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712267 | ||||||
chr20:32712269
|
C | CA | 119 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(116): Show | 129 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.242-5510dupT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712269 | ||||||
chr20:32712269
|
C | CAA | 31 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(28): Show | 36 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.242-5511_242-5510d others(4): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712269 | ||||||
chr20:32712269
|
C | CAAA | 6 | a0001c0001t0001g0025a0001c0001t0001g0134a0001c0001t0001g0277others(3): Show | 6 | HG00140.hp2 HG01891.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.242-5512_242-5510d others(5): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712269 | ||||||
chr20:32712269
|
CA | C | 6 | a0001c0001t0002g0016a0001c0001t0002g0152a0001c0001t0002g0162others(3): Show | 7 | HG00741.hp1 HG02300.hp2 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.242-5510delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712269 | ||||||
chr20:32712269
|
CAAAAAAA | C | 72 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(69): Show | 75 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(72): Show |
intron_variant | MODIFIER | c.242-5516_242-5510d others(9): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712269 | ||||||
chr20:32712293
|
A | AAAAAAAA others(8): Show |
1 | a0001c0001t0001g0109 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.242-5534_242-5533i others(17): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712293 | ||||||
chr20:32712340
|
C | A | 1 | a0001c0001t0002g0118 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.242-5580G>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712340 | ||||||
chr20:32712437
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.242-5677C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712437 | ||||||
chr20:32712465
|
G | A | 3 | a0001c0001t0002g0163a0001c0001t0002g0235a0001c0001t0002g0236 | 3 | NA18995.hp1 NA19000.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.242-5705C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712465 | ||||||
chr20:32712507
|
A | C | 3 | a0001c0001t0001g0116a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG02486.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.242-5747T>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712507 | ||||||
chr20:32712612
|
T | TA | 80 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(77): Show | 84 | HG00280.hp2 HG00423.hp1 HG00673.hp1 others(81): Show |
intron_variant | MODIFIER | c.242-5853dupT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712612 | ||||||
chr20:32712612
|
T | TAA | 10 | a0001c0001t0001g0042a0001c0001t0001g0066a0001c0001t0001g0079others(7): Show | 10 | HG01109.hp2 HG01891.hp2 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.242-5854_242-5853d others(4): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712612 | ||||||
chr20:32712612
|
T | TAAA | 132 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(129): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.242-5855_242-5853d others(5): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712612 | ||||||
chr20:32712677
|
G | A | 71 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(68): Show | 74 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.242-5917C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712677 | ||||||
chr20:32712727
|
C | CT | 209 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 228 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.242-5968dupA | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712727 | ||||||
chr20:32712727
|
C | T | 2 | a0001c0001t0001g0109a0001c0001t0006g0120 | 2 | HG01109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.242-5967G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712727 | ||||||
chr20:32712745
|
G | A | 1 | a0001c0001t0002g0239 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.242-5985C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712745 | ||||||
chr20:32712750
|
CT | C | 14 | a0001c0001t0001g0019a0001c0001t0001g0033a0001c0001t0001g0131others(11): Show | 15 | HG00280.hp2 HG00733.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.242-5991delA | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712750 | ||||||
chr20:32712750
|
CTT | C | 53 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0036others(50): Show | 55 | HG00140.hp2 HG00741.hp2 HG01074.hp1 others(52): Show |
intron_variant | MODIFIER | c.242-5992_242-5991d others(4): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712750 | ||||||
chr20:32712750
|
CTTT | C | 143 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(140): Show | 159 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.242-5993_242-5991d others(5): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712750 | ||||||
chr20:32712770
|
G | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 232 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.242-6010C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712770 | ||||||
chr20:32712875
|
C | T | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 232 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.242-6115G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32712875 | ||||||
chr20:32713049
|
CT | C | 6 | a0001c0001t0001g0066a0001c0001t0001g0109a0001c0001t0001g0110others(3): Show | 6 | HG01109.hp2 HG01167.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.242-6290delA | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32713049 | ||||||
chr20:32713125
|
T | C | 8 | a0001c0001t0002g0020a0001c0001t0002g0127a0001c0001t0002g0204others(5): Show | 8 | HG00621.hp2 HG02040.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.242-6365A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32713125 | ||||||
chr20:32713297
|
G | A | 96 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(93): Show | 103 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.242-6537C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32713297 | ||||||
chr20:32713335
|
C | T | 2 | a0001c0001t0001g0109a0001c0001t0006g0120 | 2 | HG01109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.242-6575G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32713335 | ||||||
chr20:32713342
|
G | A | 1 | a0001c0001t0001g0018 | 2 | HG00099.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.242-6582C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32713342 | ||||||
chr20:32713444
|
G | A | 1 | a0001c0001t0002g0176 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.242-6684C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32713444 | ||||||
chr20:32713446
|
C | T | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 232 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.242-6686G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32713446 | ||||||
chr20:32713600
|
T | C | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 232 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.242-6840A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32713600 | ||||||
chr20:32713653
|
G | A | 1 | a0001c0001t0003g0007 | 2 | HG02280.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.242-6893C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32713653 | ||||||
chr20:32713693
|
T | C | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 232 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.242-6933A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32713693 | ||||||
chr20:32713865
|
T | C | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 232 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.242-7105A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32713865 | ||||||
chr20:32713973
|
C | T | 1 | a0001c0001t0001g0345 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.242-7213G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32713973 | ||||||
chr20:32713993
|
A | G | 2 | a0001c0001t0001g0109a0001c0001t0006g0120 | 2 | HG01109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.242-7233T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32713993 | ||||||
chr20:32714017
|
G | A | 71 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(68): Show | 74 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.242-7257C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32714017 | ||||||
chr20:32714040
|
G | A | 1 | a0001c0001t0001g0353 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.242-7280C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32714040 | ||||||
chr20:32714062
|
G | A | 1 | a0001c0001t0001g0363 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.242-7302C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32714062 | ||||||
chr20:32714136
|
C | A | 211 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(208): Show | 230 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.242-7376G>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32714136 | ||||||
chr20:32714152
|
A | C | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 232 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.242-7392T>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32714152 | ||||||
chr20:32714195
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.242-7435C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32714195 | ||||||
chr20:32714376
|
G | A | 139 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 155 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.242-7616C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32714376 | ||||||
chr20:32714516
|
C | T | 1 | a0001c0001t0002g0206 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.242-7756G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32714516 | ||||||
chr20:32714645
|
G | A | 1 | a0001c0001t0002g0158 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.242-7885C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32714645 | ||||||
chr20:32714646
|
A | C | 1 | a0001c0001t0002g0158 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.242-7886T>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32714646 | ||||||
chr20:32714786
|
T | C | 5 | a0001c0001t0001g0072a0001c0001t0001g0100a0001c0001t0001g0101others(2): Show | 5 | HG03654.hp1 HG03688.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.242-8026A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32714786 | ||||||
chr20:32714824
|
A | AAAC | 7 | a0001c0001t0002g0113a0001c0001t0002g0114a0001c0001t0002g0115others(4): Show | 7 | HG01261.hp1 HG02647.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.242-8067_242-8065d others(5): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32714824 | ||||||
chr20:32714824
|
A | AAACAAC | 3 | a0001c0001t0001g0035a0001c0001t0001g0074a0001c0001t0001g0086 | 3 | NA18948.hp1 NA19005.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.242-8070_242-8065d others(8): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32714824 | ||||||
chr20:32714824
|
A | AAACAACA others(2): Show |
118 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(115): Show | 127 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.242-8073_242-8065d others(11): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32714824 | ||||||
chr20:32714824
|
A | AAACAACA others(5): Show |
23 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(20): Show | 28 | HG00544.hp1 HG01258.hp2 HG02027.hp1 others(25): Show |
intron_variant | MODIFIER | c.242-8076_242-8065d others(14): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32714824 | ||||||
chr20:32714824
|
A | AAACAACA others(8): Show |
38 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0051others(35): Show | 40 | HG01074.hp1 HG01074.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.242-8079_242-8065d others(17): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32714824 | ||||||
chr20:32714824
|
A | AAACAACA others(11): Show |
20 | a0001c0001t0001g0033a0001c0001t0001g0106a0001c0001t0001g0108others(17): Show | 20 | HG00280.hp2 HG01255.hp2 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.242-8082_242-8065d others(20): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32714824 | ||||||
chr20:32714824
|
A | AAACAACA others(14): Show |
1 | a0001c0001t0001g0107 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.242-8085_242-8065d others(23): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32714824 | ||||||
chr20:32714824
|
AAAC | A | 3 | a0001c0001t0001g0327a0001c0001t0001g0371a0001c0001t0002g0217 | 3 | HG00741.hp2 HG01106.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.242-8067_242-8065d others(5): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32714824 | ||||||
chr20:32714991
|
C | T | 4 | a0001c0001t0001g0024a0001c0001t0001g0266a0001c0001t0001g0268others(1): Show | 4 | HG02145.hp1 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.242-8231G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32714991 | ||||||
chr20:32715017
|
T | C | 71 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(68): Show | 74 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.242-8257A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32715017 | ||||||
chr20:32715022
|
A | T | 1 | a0001c0001t0002g0228 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.242-8262T>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32715022 | ||||||
chr20:32715023
|
T | A | 1 | a0001c0001t0002g0228 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.242-8263A>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32715023 | ||||||
chr20:32715025
|
A | AAAATAAA others(3): Show |
8 | a0001c0001t0001g0124a0001c0001t0001g0303a0001c0001t0001g0305others(5): Show | 8 | HG02040.hp2 NA18942.hp2 NA18945.hp2 others(5): Show |
intron_variant | MODIFIER | c.242-8266_242-8265i others(12): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32715025 | ||||||
chr20:32715027
|
A | AATAAAT | 21 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0022others(18): Show | 23 | HG01167.hp2 HG01243.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.242-8273_242-8268d others(8): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32715027 | ||||||
chr20:32715100
|
C | A | 14 | a0001c0001t0001g0035a0001c0001t0001g0066a0001c0001t0001g0068others(11): Show | 14 | HG00558.hp2 HG00673.hp2 NA18940.hp2 others(11): Show |
intron_variant | MODIFIER | c.242-8340G>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32715100 | ||||||
chr20:32715221
|
T | C | 3 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0276 | 3 | HG02145.hp1 HG03139.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.242-8461A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32715221 | ||||||
chr20:32715486
|
A | AAAAC | 211 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(208): Show | 230 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.242-8730_242-8727d others(6): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32715486 | ||||||
chr20:32715589
|
T | C | 102 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(99): Show | 109 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.242-8829A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32715589 | ||||||
chr20:32715628
|
G | A | 52 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0033others(49): Show | 54 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(51): Show |
intron_variant | MODIFIER | c.242-8868C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32715628 | ||||||
chr20:32715700
|
G | A | 34 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(31): Show | 43 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(40): Show |
intron_variant | MODIFIER | c.242-8940C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32715700 | ||||||
chr20:32715839
|
T | A | 1 | a0001c0001t0005g0359 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.242-9079A>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32715839 | ||||||
chr20:32716140
|
T | C | 211 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(208): Show | 230 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.242-9380A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32716140 | ||||||
chr20:32716337
|
C | T | 1 | a0001c0001t0003g0007 | 2 | HG02280.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.242-9577G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32716337 | ||||||
chr20:32716411
|
C | T | 1 | a0001c0001t0001g0041 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.242-9651G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32716411 | ||||||
chr20:32716442
|
T | C | 1 | a0001c0001t0001g0149 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.242-9682A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32716442 | ||||||
chr20:32716507
|
T | C | 3 | a0001c0001t0002g0254a0001c0001t0002g0255a0001c0001t0002g0256 | 3 | HG01109.hp1 HG02055.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.242-9747A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32716507 | ||||||
chr20:32716601
|
T | C | 211 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(208): Show | 230 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.242-9841A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32716601 | ||||||
chr20:32716690
|
A | C | 1 | a0001c0001t0001g0080 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.242-9930T>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32716690 | ||||||
chr20:32716854
|
A | G | 1 | a0001c0001t0001g0099 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.242-10094T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32716854 | ||||||
chr20:32716859
|
C | CT | 6 | a0001c0001t0001g0116a0001c0001t0001g0133a0001c0001t0001g0134others(3): Show | 6 | HG02486.hp2 HG02965.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.242-10100dupA | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32716859 | ||||||
chr20:32716859
|
CT | C | 75 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(72): Show | 78 | HG00280.hp2 HG00639.hp2 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.242-10100delA | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32716859 | ||||||
chr20:32716911
|
C | T | 211 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(208): Show | 230 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.242-10151G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32716911 | ||||||
chr20:32716935
|
C | T | 1 | a0001c0001t0002g0193 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.242-10175G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32716935 | ||||||
chr20:32716940
|
C | T | 18 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(15): Show | 23 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(20): Show |
intron_variant | MODIFIER | c.242-10180G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32716940 | ||||||
chr20:32717011
|
G | T | 211 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(208): Show | 230 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.242-10251C>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32717011 | ||||||
chr20:32717192
|
G | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(205): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.242-10432C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32717192 | ||||||
chr20:32717321
|
A | AT | 11 | a0001c0001t0002g0030a0001c0001t0002g0158a0001c0001t0002g0192others(8): Show | 11 | HG00673.hp1 HG00741.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.242-10562dupA | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32717321 | ||||||
chr20:32717321
|
AT | A | 8 | a0001c0001t0002g0020a0001c0001t0002g0157a0001c0001t0002g0159others(5): Show | 8 | HG01167.hp1 HG01975.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.242-10562delA | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32717321 | ||||||
chr20:32717321
|
ATTTTT | A | 107 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(104): Show | 119 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.242-10566_242-1056 others(9): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32717321 | ||||||
chr20:32717321
|
ATTTTTT | A | 96 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(93): Show | 103 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.241+10566_242-1056 others(10): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32717321 | ||||||
chr20:32717382
|
G | A | 45 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(42): Show | 50 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.241+10511C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32717382 | ||||||
chr20:32717413
|
C | T | 1 | a0001c0001t0002g0153 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.241+10480G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32717413 | ||||||
chr20:32717532
|
G | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0087a0001c0001t0001g0089others(4): Show | 11 | HG00544.hp1 HG02027.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.241+10361C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32717532 | ||||||
chr20:32717627
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.241+10266T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32717627 | ||||||
chr20:32717839
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(205): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.241+10054A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32717839 | ||||||
chr20:32717896
|
C | G | 1 | a0001c0001t0001g0266 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.241+9997G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32717896 | ||||||
chr20:32718065
|
G | A | 207 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(204): Show | 226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.241+9828C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718065 | ||||||
chr20:32718068
|
G | A | 1 | a0001c0001t0001g0306 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.241+9825C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718068 | ||||||
chr20:32718088
|
C | CA | 16 | a0001c0001t0001g0300a0001c0001t0002g0015a0001c0001t0002g0152others(13): Show | 17 | HG00423.hp1 HG00673.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.241+9804dupT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718088 | ||||||
chr20:32718088
|
CA | C | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(197): Show | 216 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.241+9804delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718088 | ||||||
chr20:32718122
|
G | A | 1 | a0001c0001t0001g0363 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.241+9771C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718122 | ||||||
chr20:32718200
|
C | T | 1 | a0001c0001t0003g0007 | 2 | HG02280.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.241+9693G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718200 | ||||||
chr20:32718231
|
C | T | 1 | a0001c0001t0002g0009 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.241+9662G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718231 | ||||||
chr20:32718272
|
C | T | 4 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0030others(1): Show | 4 | HG01361.hp2 HG02615.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.241+9621G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718272 | ||||||
chr20:32718353
|
G | C | 63 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(60): Show | 66 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.241+9540C>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718353 | ||||||
chr20:32718412
|
A | G | 1 | a0001c0001t0002g0229 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.241+9481T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718412 | ||||||
chr20:32718413
|
G | A | 207 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(204): Show | 226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.241+9480C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718413 | ||||||
chr20:32718424
|
C | T | 2 | a0001c0001t0002g0289a0001c0001t0002g0290 | 2 | HG02055.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.241+9469G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718424 | ||||||
chr20:32718497
|
G | A | 1 | a0001c0001t0002g0227 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.241+9396C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718497 | ||||||
chr20:32718507
|
T | C | 1 | a0001c0001t0001g0024 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.241+9386A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718507 | ||||||
chr20:32718515
|
A | G | 1 | a0001c0001t0001g0363 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.241+9378T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718515 | ||||||
chr20:32718549
|
A | C | 1 | a0001c0001t0002g0253 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.241+9344T>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718549 | ||||||
chr20:32718607
|
G | A | 2 | a0001c0001t0002g0016a0001c0001t0002g0150 | 3 | NA18995.hp2 NA19054.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.241+9286C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718607 | ||||||
chr20:32718631
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.241+9262C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718631 | ||||||
chr20:32718710
|
T | C | 3 | a0001c0001t0001g0116a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG02486.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.241+9183A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718710 | ||||||
chr20:32718729
|
T | C | 97 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(94): Show | 104 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.241+9164A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718729 | ||||||
chr20:32718780
|
C | CA | 10 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0073others(7): Show | 13 | HG01123.hp2 HG02451.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.241+9112dupT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718780 | ||||||
chr20:32718814
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.241+9079A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718814 | ||||||
chr20:32718830
|
G | A | 2 | a0001c0001t0002g0111a0001c0001t0002g0112 | 2 | HG00099.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.241+9063C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718830 | ||||||
chr20:32718912
|
C | T | 1 | a0001c0001t0001g0363 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.241+8981G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718912 | ||||||
chr20:32718923
|
T | C | 63 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(60): Show | 66 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.241+8970A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718923 | ||||||
chr20:32718926
|
C | G | 211 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(208): Show | 230 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.241+8967G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32718926 | ||||||
chr20:32719059
|
G | A | 33 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(30): Show | 42 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(39): Show |
intron_variant | MODIFIER | c.241+8834C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32719059 | ||||||
chr20:32719099
|
C | A | 1 | a0001c0001t0001g0141 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.241+8794G>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32719099 | ||||||
chr20:32719271
|
T | C | 1 | a0001c0001t0001g0011 | 2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.241+8622A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32719271 | ||||||
chr20:32719275
|
C | T | 1 | a0001c0001t0002g0224 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.241+8618G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32719275 | ||||||
chr20:32719409
|
A | G | 1 | a0001c0001t0002g0288 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.241+8484T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32719409 | ||||||
chr20:32719477
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.241+8416G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32719477 | ||||||
chr20:32719822
|
C | T | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | HG02486.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.241+8071G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32719822 | ||||||
chr20:32719905
|
G | A | 1 | a0001c0001t0002g0252 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.241+7988C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32719905 | ||||||
chr20:32719950
|
A | G | 6 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0121others(3): Show | 9 | HG02451.hp1 HG02809.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.241+7943T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32719950 | ||||||
chr20:32720232
|
C | T | 1 | a0001c0001t0002g0009 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.241+7661G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32720232 | ||||||
chr20:32720233
|
G | A | 1 | a0001c0001t0009g0287 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.241+7660C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32720233 | ||||||
chr20:32720237
|
A | G | 211 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(208): Show | 230 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.241+7656T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32720237 | ||||||
chr20:32720377
|
C | A | 1 | a0001c0001t0001g0043 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.241+7516G>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32720377 | ||||||
chr20:32720387
|
C | T | 1 | a0001c0001t0005g0359 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.241+7506G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32720387 | ||||||
chr20:32720594
|
A | G | 360 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(357): Show | 385 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(382): Show |
intron_variant | MODIFIER | c.241+7299T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32720594 | ||||||
chr20:32720637
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.241+7256G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32720637 | ||||||
chr20:32720638
|
G | A | 3 | a0001c0001t0002g0152a0001c0001t0002g0184a0001c0001t0002g0220 | 3 | NA18942.hp1 NA18944.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.241+7255C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32720638 | ||||||
chr20:32720701
|
G | A | 2 | a0001c0001t0002g0020a0001c0001t0002g0127 | 2 | HG00621.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.241+7192C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32720701 | ||||||
chr20:32720856
|
T | C | 1 | a0001c0001t0002g0191 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.241+7037A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32720856 | ||||||
chr20:32720857
|
A | T | 1 | a0001c0001t0002g0191 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.241+7036T>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32720857 | ||||||
chr20:32720881
|
C | T | 211 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(208): Show | 230 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.241+7012G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32720881 | ||||||
chr20:32721091
|
G | A | 3 | a0001c0001t0001g0116a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG02486.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.241+6802C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32721091 | ||||||
chr20:32721199
|
C | T | 3 | a0001c0001t0001g0116a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG02486.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.241+6694G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32721199 | ||||||
chr20:32721251
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(205): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.241+6642A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32721251 | ||||||
chr20:32721289
|
C | T | 1 | a0001c0001t0005g0359 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.241+6604G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32721289 | ||||||
chr20:32721522
|
A | G | 1 | a0001c0001t0002g0254 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.241+6371T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32721522 | ||||||
chr20:32721809
|
T | C | 2 | a0001c0001t0001g0109a0001c0001t0006g0120 | 2 | HG01109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.241+6084A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32721809 | ||||||
chr20:32721896
|
CA | C | 207 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(204): Show | 226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.241+5996delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32721896 | ||||||
chr20:32721986
|
G | A | 8 | a0001c0001t0001g0003a0001c0001t0001g0041a0001c0001t0001g0042others(5): Show | 10 | NA18946.hp2 NA18960.hp2 NA18962.hp1 others(7): Show |
intron_variant | MODIFIER | c.241+5907C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32721986 | ||||||
chr20:32721993
|
G | A | 21 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0023others(18): Show | 23 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.241+5900C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32721993 | ||||||
chr20:32722103
|
G | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(205): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.241+5790C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32722103 | ||||||
chr20:32722138
|
G | A | 1 | a0001c0001t0002g0118 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.241+5755C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32722138 | ||||||
chr20:32722173
|
C | T | 1 | a0001c0001t0001g0299 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.241+5720G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32722173 | ||||||
chr20:32722246
|
G | GA | 210 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(207): Show | 223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.241+5646dupT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32722246 | ||||||
chr20:32722246
|
G | GAA | 47 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0022others(44): Show | 49 | HG01109.hp2 HG01167.hp2 HG01243.hp2 others(46): Show |
intron_variant | MODIFIER | c.241+5645_241+5646d others(4): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32722246 | ||||||
chr20:32722246
|
G | GAAA | 63 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0025others(60): Show | 68 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.241+5644_241+5646d others(5): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32722246 | ||||||
chr20:32722246
|
GA | G | 6 | a0001c0001t0001g0012a0001c0001t0001g0121a0001c0001t0001g0122others(3): Show | 7 | HG00140.hp2 HG02300.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.241+5646delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32722246 | ||||||
chr20:32722276
|
G | C | 10 | a0001c0001t0002g0113a0001c0001t0002g0114a0001c0001t0002g0115others(7): Show | 10 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.241+5617C>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32722276 | ||||||
chr20:32722347
|
G | A | 1 | a0001c0001t0002g0027 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.241+5546C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32722347 | ||||||
chr20:32722411
|
G | A | 1 | a0001c0001t0001g0312 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.241+5482C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32722411 | ||||||
chr20:32722478
|
G | A | 1 | a0001c0001t0003g0007 | 2 | HG02280.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.241+5415C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32722478 | ||||||
chr20:32722648
|
C | T | 3 | a0001c0001t0001g0116a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG02486.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.241+5245G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32722648 | ||||||
chr20:32722649
|
G | A | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0275 | 3 | HG00408.hp1 HG02155.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.241+5244C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32722649 | ||||||
chr20:32722720
|
GA | G | 13 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0051others(10): Show | 14 | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.241+5172delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32722720 | ||||||
chr20:32722902
|
G | T | 1 | a0001c0001t0001g0099 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.241+4991C>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32722902 | ||||||
chr20:32722936
|
G | A | 2 | a0001c0001t0001g0019a0001c0001t0001g0343 | 3 | HG01516.hp2 HG01517.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.241+4957C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32722936 | ||||||
chr20:32722940
|
A | C | 1 | a0001c0001t0002g0238 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.241+4953T>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32722940 | ||||||
chr20:32722976
|
G | A | 97 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(94): Show | 104 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.241+4917C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32722976 | ||||||
chr20:32723045
|
A | AAAT | 156 | a0001c0001t0001g0109a0001c0001t0001g0221a0001c0001t0002g0002others(153): Show | 165 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.241+4845_241+4847d others(5): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723045 | ||||||
chr20:32723048
|
T | TA | 127 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(124): Show | 143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.241+4844dupT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723048 | ||||||
chr20:32723050
|
A | AAT | 7 | a0001c0001t0001g0068a0001c0001t0001g0075a0001c0001t0001g0136others(4): Show | 7 | HG00558.hp2 HG02258.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.241+4842_241+4843i others(4): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723050 | ||||||
chr20:32723051
|
T | A | 7 | a0001c0001t0001g0068a0001c0001t0001g0075a0001c0001t0001g0136others(4): Show | 7 | HG00558.hp2 HG02258.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.241+4842A>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723051 | ||||||
chr20:32723057
|
T | A | 6 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0121others(3): Show | 9 | HG02451.hp1 HG02809.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.241+4836A>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723057 | ||||||
chr20:32723063
|
TAAAGACT others(1886): Show |
T | 1 | a0001c0001t0001g0364 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.241+2937_241+4829d others(2): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723063 | ||||||
chr20:32723063
|
TAAAGACT others(1889): Show |
T | 11 | a0001c0001t0001g0119a0001c0001t0001g0129a0001c0001t0001g0130others(8): Show | 11 | HG01891.hp1 HG01934.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.241+2934_241+4829d others(2): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723063 | ||||||
chr20:32723063
|
TAAAGACT others(1892): Show |
T | 61 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(58): Show | 72 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.241+2931_241+4829d others(2): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723063 | ||||||
chr20:32723063
|
TAAAGACT others(1895): Show |
T | 133 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0010others(130): Show | 141 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.241+2928_241+4829d others(2): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723063 | ||||||
chr20:32723063
|
TAAAGACT others(1898): Show |
T | 5 | a0001c0001t0001g0116a0001c0001t0001g0133a0001c0001t0001g0134others(2): Show | 5 | HG00733.hp2 HG02486.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.241+2925_241+4829d others(2): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723063 | ||||||
chr20:32723076
|
T | TCCTCTC | 9 | a0001c0001t0002g0219a0001c0001t0002g0244a0001c0001t0002g0254others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.241+4811_241+4816d others(8): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723076 | ||||||
chr20:32723076
|
T | TCCTCTCC others(5): Show |
1 | a0001c0001t0001g0109 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.241+4805_241+4816d others(14): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723076 | ||||||
chr20:32723090
|
CTCTCCCT others(5): Show |
C | 3 | a0001c0001t0002g0156a0001c0001t0002g0157a0001c0001t0002g0181 | 3 | HG00738.hp2 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.241+4791_241+4802d others(14): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723090 | ||||||
chr20:32723102
|
G | C | 1 | a0001c0001t0009g0287 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.241+4791C>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723102 | ||||||
chr20:32723108
|
C | G | 1 | a0001c0001t0009g0287 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.241+4785G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723108 | ||||||
chr20:32723125
|
C | CCTCTCCC others(23): Show |
1 | a0001c0001t0009g0287 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.241+4767_241+4768i others(32): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723125 | ||||||
chr20:32723129
|
C | T | 2 | a0001c0001t0001g0109a0001c0001t0006g0120 | 2 | HG01109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.241+4764G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723129 | ||||||
chr20:32723130
|
C | G | 1 | a0001c0001t0009g0287 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.241+4763G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723130 | ||||||
chr20:32723131
|
T | C | 2 | a0001c0001t0001g0109a0001c0001t0006g0120 | 2 | HG01109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.241+4762A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723131 | ||||||
chr20:32723135
|
C | G | 1 | a0001c0001t0002g0240 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.241+4758G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723135 | ||||||
chr20:32723136
|
G | C | 2 | a0001c0001t0001g0109a0001c0001t0006g0120 | 2 | HG01109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.241+4757C>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723136 | ||||||
chr20:32723176
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.241+4717C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723176 | ||||||
chr20:32723197
|
C | T | 2 | a0001c0001t0002g0284a0001c0001t0002g0366 | 2 | HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.241+4696G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723197 | ||||||
chr20:32723227
|
C | G | 3 | a0001c0001t0002g0231a0001c0001t0002g0232a0001c0001t0002g0233 | 3 | HG02129.hp1 NA18964.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.241+4666G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723227 | ||||||
chr20:32723270
|
GAGTGCCT others(8): Show |
G | 4 | a0001c0001t0002g0219a0001c0001t0002g0254a0001c0001t0002g0255others(1): Show | 4 | HG01109.hp1 HG02055.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.241+4608_241+4622d others(17): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723270 | ||||||
chr20:32723292
|
G | A | 7 | a0001c0001t0002g0020a0001c0001t0002g0127a0001c0001t0002g0204others(4): Show | 7 | HG00621.hp2 HG02040.hp1 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.241+4601C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723292 | ||||||
chr20:32723324
|
C | T | 3 | a0001c0001t0002g0254a0001c0001t0002g0255a0001c0001t0002g0256 | 3 | HG01109.hp1 HG02055.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.241+4569G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723324 | ||||||
chr20:32723406
|
G | A | 1 | a0001c0001t0002g0216 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.241+4487C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723406 | ||||||
chr20:32723554
|
A | AC | 19 | a0001c0001t0002g0029a0001c0001t0002g0114a0001c0001t0002g0115others(16): Show | 19 | HG00741.hp1 HG01358.hp1 HG02615.hp1 others(16): Show |
intron_variant | MODIFIER | c.241+4338dupG | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723554 | ||||||
chr20:32723660
|
C | A | 8 | a0001c0001t0002g0063a0001c0001t0002g0160a0001c0001t0002g0161others(5): Show | 8 | HG01070.hp2 NA18944.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.241+4233G>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723660 | ||||||
chr20:32723742
|
C | T | 5 | a0001c0001t0002g0113a0001c0001t0002g0114a0001c0001t0002g0115others(2): Show | 5 | HG01261.hp1 HG02647.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.241+4151G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723742 | ||||||
chr20:32723822
|
C | A | 1 | a0001c0001t0002g0242 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.241+4071G>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723822 | ||||||
chr20:32723891
|
T | C | 2 | a0001c0001t0002g0244a0001c0001t0002g0285 | 2 | HG02922.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.241+4002A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32723891 | ||||||
chr20:32724012
|
G | A | 10 | a0001c0001t0002g0015a0001c0001t0002g0152a0001c0001t0002g0158others(7): Show | 11 | HG00423.hp1 HG00673.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.241+3881C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32724012 | ||||||
chr20:32724046
|
G | T | 1 | a0001c0001t0002g0366 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.241+3847C>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32724046 | ||||||
chr20:32724131
|
A | G | 160 | a0001c0001t0001g0109a0001c0001t0001g0221a0001c0001t0002g0002others(157): Show | 169 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.241+3762T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32724131 | ||||||
chr20:32724158
|
C | G | 1 | a0001c0001t0002g0175 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.241+3735G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32724158 | ||||||
chr20:32724174
|
C | T | 1 | a0001c0001t0002g0288 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.241+3719G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32724174 | ||||||
chr20:32724180
|
GGGAGGTG others(168): Show |
G | 1 | a0001c0001t0002g0111 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.241+3538_241+3712d others(2): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32724180 | ||||||
chr20:32724302
|
G | A | 1 | a0001c0001t0002g0334 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.241+3591C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32724302 | ||||||
chr20:32724323
|
G | A | 1 | a0001c0001t0002g0185 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.241+3570C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32724323 | ||||||
chr20:32724951
|
T | A | 4 | a0001c0001t0001g0109a0001c0001t0002g0023a0001c0001t0006g0120others(1): Show | 4 | HG00741.hp1 HG01109.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.241+2942A>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32724951 | ||||||
chr20:32724951
|
T | TA | 6 | a0001c0001t0001g0221a0001c0001t0002g0171a0001c0001t0002g0174others(3): Show | 6 | HG00438.hp2 HG00544.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.241+2941dupT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32724951 | ||||||
chr20:32724951
|
TA | T | 9 | a0001c0001t0002g0028a0001c0001t0002g0034a0001c0001t0002g0157others(6): Show | 9 | HG00140.hp1 HG01167.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.241+2941delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32724951 | ||||||
chr20:32724959
|
A | T | 1 | a0001c0001t0001g0364 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.241+2934T>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32724959 | ||||||
chr20:32724962
|
A | T | 12 | a0001c0001t0001g0119a0001c0001t0001g0129a0001c0001t0001g0130others(9): Show | 12 | HG01891.hp1 HG01934.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.241+2931T>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32724962 | ||||||
chr20:32724965
|
A | T | 73 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(70): Show | 84 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.241+2928T>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32724965 | ||||||
chr20:32724968
|
A | T | 206 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(203): Show | 225 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.241+2925T>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32724968 | ||||||
chr20:32724971
|
A | T | 211 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(208): Show | 230 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.241+2922T>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32724971 | ||||||
chr20:32725030
|
C | A | 7 | a0001c0001t0003g0295a0001c0001t0003g0296a0001c0001t0003g0369others(4): Show | 7 | HG02630.hp1 HG02886.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.241+2863G>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32725030 | ||||||
chr20:32725076
|
T | C | 1 | a0001c0001t0002g0188 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.241+2817A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32725076 | ||||||
chr20:32725109
|
A | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(205): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.241+2784T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32725109 | ||||||
chr20:32725120
|
C | G | 2 | a0001c0001t0001g0129a0001c0001t0001g0130 | 2 | HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.241+2773G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32725120 | ||||||
chr20:32725258
|
G | A | 61 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0035others(58): Show | 66 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.241+2635C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32725258 | ||||||
chr20:32725356
|
C | G | 1 | a0001c0001t0001g0128 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.241+2537G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32725356 | ||||||
chr20:32725384
|
A | C | 3 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0030 | 3 | HG01361.hp2 HG02615.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.241+2509T>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32725384 | ||||||
chr20:32725431
|
G | GT | 11 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0137others(8): Show | 11 | HG00438.hp2 HG01167.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.241+2461dupA | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32725431 | ||||||
chr20:32725431
|
G | GTT | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 179 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.241+2460_241+2461d others(4): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32725431 | ||||||
chr20:32725431
|
G | GTTT | 36 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(33): Show | 41 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.241+2459_241+2461d others(5): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32725431 | ||||||
chr20:32725435
|
T | TG | 3 | a0001c0001t0001g0116a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG02486.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.241+2457_241+2458i others(3): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32725435 | ||||||
chr20:32725491
|
C | T | 72 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(69): Show | 75 | HG00280.hp2 HG00741.hp2 HG01074.hp1 others(72): Show |
intron_variant | MODIFIER | c.241+2402G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32725491 | ||||||
chr20:32725503
|
A | C | 5 | a0001c0001t0001g0025a0001c0001t0001g0277a0001c0001t0001g0278others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.241+2390T>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32725503 | ||||||
chr20:32725529
|
C | T | 1 | a0002c0002t0001g0077 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.241+2364G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32725529 | ||||||
chr20:32725636
|
G | A | 31 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0022others(28): Show | 33 | HG01167.hp2 HG01243.hp2 HG02040.hp2 others(30): Show |
intron_variant | MODIFIER | c.241+2257C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32725636 | ||||||
chr20:32725689
|
A | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0121others(3): Show | 9 | HG02451.hp1 HG02809.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.241+2204T>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32725689 | ||||||
chr20:32725840
|
C | G | 3 | a0001c0001t0001g0116a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG02486.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.241+2053G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32725840 | ||||||
chr20:32725843
|
G | A | 1 | a0001c0001t0001g0363 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.241+2050C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32725843 | ||||||
chr20:32725930
|
G | A | 92 | a0001c0001t0001g0221a0001c0001t0002g0009a0001c0001t0002g0013others(89): Show | 96 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.241+1963C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32725930 | ||||||
chr20:32725969
|
G | A | 2 | a0001c0001t0001g0109a0001c0001t0006g0120 | 2 | HG01109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.241+1924C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32725969 | ||||||
chr20:32725974
|
G | A | 2 | a0001c0001t0002g0063a0001c0001t0002g0164 | 2 | NA18944.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.241+1919C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32725974 | ||||||
chr20:32726000
|
T | G | 1 | a0001c0001t0003g0295 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.241+1893A>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32726000 | ||||||
chr20:32726062
|
C | CA | 12 | a0001c0001t0001g0221a0001c0001t0002g0118a0001c0001t0002g0158others(9): Show | 12 | HG00438.hp2 HG00673.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.241+1830dupT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32726062 | ||||||
chr20:32726062
|
CA | C | 168 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(165): Show | 179 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.241+1830delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32726062 | ||||||
chr20:32726121
|
T | G | 9 | a0001c0001t0001g0337a0001c0001t0001g0338a0001c0001t0001g0339others(6): Show | 9 | HG01074.hp2 HG01192.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.241+1772A>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32726121 | ||||||
chr20:32726172
|
G | A | 2 | a0001c0001t0002g0113a0001c0001t0002g0115 | 2 | HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.241+1721C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32726172 | ||||||
chr20:32726190
|
C | G | 1 | a0001c0001t0005g0359 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.241+1703G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32726190 | ||||||
chr20:32726259
|
C | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0106a0001c0001t0001g0107others(2): Show | 6 | HG01358.hp2 HG02615.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.241+1634G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32726259 | ||||||
chr20:32726465
|
A | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(205): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.241+1428T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32726465 | ||||||
chr20:32726466
|
C | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(205): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.241+1427G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32726466 | ||||||
chr20:32726477
|
G | T | 3 | a0001c0001t0001g0116a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG02486.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.241+1416C>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32726477 | ||||||
chr20:32726622
|
G | C | 1 | a0001c0001t0005g0359 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.241+1271C>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32726622 | ||||||
chr20:32726640
|
T | C | 2 | a0001c0001t0001g0109a0001c0001t0006g0120 | 2 | HG01109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.241+1253A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32726640 | ||||||
chr20:32726781
|
C | T | 4 | a0001c0001t0001g0243a0001c0001t0002g0254a0001c0001t0002g0255others(1): Show | 4 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.241+1112G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32726781 | ||||||
chr20:32726818
|
A | G | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 232 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.241+1075T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32726818 | ||||||
chr20:32726950
|
C | G | 211 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(208): Show | 230 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.241+943G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32726950 | ||||||
chr20:32727120
|
T | TG | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(205): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.241+772dupC | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32727120 | ||||||
chr20:32727133
|
G | A | 211 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(208): Show | 230 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.241+760C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32727133 | ||||||
chr20:32727286
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.241+607G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32727286 | ||||||
chr20:32727346
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(205): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.241+547A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32727346 | ||||||
chr20:32727351
|
A | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(205): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.241+542T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32727351 | ||||||
chr20:32727458
|
C | A | 1 | a0001c0001t0001g0117 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.241+435G>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32727458 | ||||||
chr20:32727534
|
C | CA | 115 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(112): Show | 126 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.241+358dupT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32727534 | ||||||
chr20:32727534
|
CA | C | 15 | a0001c0001t0001g0011a0001c0001t0001g0106a0001c0001t0001g0107others(12): Show | 16 | HG01069.hp2 HG01169.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.241+358delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32727534 | ||||||
chr20:32727543
|
A | G | 3 | a0001c0001t0001g0116a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG02486.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.241+350T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32727543 | ||||||
chr20:32727563
|
T | A | 3 | a0001c0001t0001g0116a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG02486.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.241+330A>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32727563 | ||||||
chr20:32727684
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.241+209G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32727684 | ||||||
chr20:32727687
|
GCTGTGCT others(4): Show |
G | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(205): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.241+195_241+205del others(11): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32727687 | ||||||
chr20:32727773
|
C | T | 2 | a0001c0001t0002g0170a0001c0001t0002g0171 | 2 | HG00438.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.241+120G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 3/8 | chr20 | 32727773 | ||||||
chr20:32728018
|
A | G | 3 | a0001c0001t0001g0116a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG02486.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.139-23T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 2/8 | chr20 | 32728018 | ||||||
chr20:32728054
|
C | T | 1 | a0001c0001t0001g0351 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.138+35G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 2/8 | chr20 | 32728054 | ||||||
chr20:32728055
|
G | A | 97 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(94): Show | 104 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.138+34C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 2/8 | chr20 | 32728055 | ||||||
chr20:32728060
|
C | T | 102 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(99): Show | 109 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.138+29G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 2/8 | chr20 | 32728060 | ||||||
chr20:32728208
|
G | GGCTAT | 9 | a0001c0001t0001g0008a0001c0001t0001g0051a0001c0001t0001g0052others(6): Show | 10 | NA18946.hp1 NA18950.hp2 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.85-67_85-66insATAG others(1): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32728208 | ||||||
chr20:32728212
|
A | G | 9 | a0001c0001t0001g0008a0001c0001t0001g0051a0001c0001t0001g0052others(6): Show | 10 | NA18946.hp1 NA18950.hp2 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.85-70T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32728212 | ||||||
chr20:32728213
|
C | T | 9 | a0001c0001t0001g0008a0001c0001t0001g0051a0001c0001t0001g0052others(6): Show | 10 | NA18946.hp1 NA18950.hp2 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.85-71G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32728213 | ||||||
chr20:32728447
|
T | G | 1 | a0001c0001t0006g0120 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.85-305A>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32728447 | ||||||
chr20:32728447
|
TACAC | T | 57 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(54): Show | 60 | HG00280.hp2 HG00741.hp2 HG01074.hp1 others(57): Show |
intron_variant | MODIFIER | c.85-309_85-306delGT others(2): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32728447 | ||||||
chr20:32728447
|
TACACAC | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(151): Show | 170 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.85-311_85-306delGT others(4): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32728447 | ||||||
chr20:32728480
|
G | A | 211 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(208): Show | 230 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.85-338C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32728480 | ||||||
chr20:32728679
|
ACCTCAGC | A | 102 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(99): Show | 109 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.85-544_85-538delGC others(5): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32728679 | ||||||
chr20:32728930
|
G | C | 8 | a0001c0001t0003g0007a0001c0001t0003g0295a0001c0001t0003g0296others(5): Show | 9 | HG02280.hp1 HG02630.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.85-788C>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32728930 | ||||||
chr20:32728960
|
T | G | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 232 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.85-818A>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32728960 | ||||||
chr20:32729055
|
C | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(205): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.85-913G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32729055 | ||||||
chr20:32729099
|
A | C | 1 | a0001c0001t0001g0125 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.85-957T>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32729099 | ||||||
chr20:32729167
|
A | AT | 75 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0035others(72): Show | 80 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.85-1026dupA | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32729167 | ||||||
chr20:32729167
|
A | ATT | 9 | a0001c0001t0001g0038a0001c0001t0001g0070a0001c0001t0001g0074others(6): Show | 9 | HG00673.hp2 HG00733.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.85-1027_85-1026dup others(2): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32729167 | ||||||
chr20:32729167
|
AT | A | 17 | a0001c0001t0001g0025a0001c0001t0001g0125a0001c0001t0001g0277others(14): Show | 17 | HG01070.hp1 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.85-1026delA | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32729167 | ||||||
chr20:32729229
|
T | A | 3 | a0001c0001t0002g0032a0001c0001t0002g0154a0001c0001t0002g0288 | 3 | HG02622.hp1 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.85-1087A>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32729229 | ||||||
chr20:32729293
|
C | A | 60 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(57): Show | 63 | HG00280.hp2 HG00741.hp2 HG01074.hp1 others(60): Show |
intron_variant | MODIFIER | c.85-1151G>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32729293 | ||||||
chr20:32729463
|
C | T | 1 | a0001c0001t0002g0159 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.85-1321G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32729463 | ||||||
chr20:32729518
|
C | T | 1 | a0001c0001t0002g0210 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.85-1376G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32729518 | ||||||
chr20:32729616
|
T | TA | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 216 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.85-1475dupT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32729616 | ||||||
chr20:32729854
|
CAA | C | 127 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(124): Show | 142 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.85-1714_85-1713del others(2): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32729854 | ||||||
chr20:32729873
|
C | T | 1 | a0001c0001t0002g0361 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.85-1731G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32729873 | ||||||
chr20:32729921
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.85-1779C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32729921 | ||||||
chr20:32730095
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.85-1953C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32730095 | ||||||
chr20:32730110
|
A | G | 2 | a0001c0001t0001g0109a0001c0001t0006g0120 | 2 | HG01109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.85-1968T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32730110 | ||||||
chr20:32730110
|
AGCCTGAG others(42): Show |
A | 6 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0132others(3): Show | 6 | HG00733.hp2 HG01192.hp1 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.85-2017_85-1969del others(49): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32730110 | ||||||
chr20:32730123
|
T | C | 1 | a0001c0001t0002g0210 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.85-1981A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32730123 | ||||||
chr20:32730144
|
ATCATGTC others(42): Show |
A | 18 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(15): Show | 23 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(20): Show |
intron_variant | MODIFIER | c.85-2051_85-2003del others(49): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32730144 | ||||||
chr20:32730265
|
T | A | 102 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(99): Show | 109 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.85-2123A>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32730265 | ||||||
chr20:32730280
|
C | T | 1 | a0001c0001t0001g0339 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.85-2138G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32730280 | ||||||
chr20:32730282
|
C | T | 1 | a0001c0001t0001g0363 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.85-2140G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32730282 | ||||||
chr20:32730297
|
G | A | 3 | a0001c0001t0001g0116a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG02486.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.85-2155C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32730297 | ||||||
chr20:32730329
|
C | T | 1 | a0001c0001t0005g0359 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.85-2187G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32730329 | ||||||
chr20:32730424
|
G | A | 1 | a0001c0001t0002g0211 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.85-2282C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32730424 | ||||||
chr20:32730442
|
C | T | 7 | a0001c0001t0003g0295a0001c0001t0003g0296a0001c0001t0003g0369others(4): Show | 7 | HG02630.hp1 HG02886.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.85-2300G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32730442 | ||||||
chr20:32730489
|
A | G | 1 | a0001c0001t0001g0147 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.85-2347T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32730489 | ||||||
chr20:32730527
|
C | G | 3 | a0001c0001t0001g0116a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG02486.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.85-2385G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32730527 | ||||||
chr20:32730558
|
A | AAAC | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(197): Show | 218 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.85-2419_85-2417dup others(3): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32730558 | ||||||
chr20:32730592
|
A | T | 1 | a0001c0001t0005g0359 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.85-2450T>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32730592 | ||||||
chr20:32730596
|
T | C | 70 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(67): Show | 73 | HG00280.hp2 HG00741.hp2 HG01074.hp1 others(70): Show |
intron_variant | MODIFIER | c.85-2454A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32730596 | ||||||
chr20:32730597
|
G | A | 70 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(67): Show | 73 | HG00280.hp2 HG00741.hp2 HG01074.hp1 others(70): Show |
intron_variant | MODIFIER | c.85-2455C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32730597 | ||||||
chr20:32730632
|
T | G | 1 | a0001c0001t0005g0359 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.85-2490A>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32730632 | ||||||
chr20:32730921
|
C | T | 18 | a0001c0001t0002g0063a0001c0001t0002g0155a0001c0001t0002g0160others(15): Show | 18 | HG01070.hp2 HG02129.hp1 HG04199.hp1 others(15): Show |
intron_variant | MODIFIER | c.85-2779G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32730921 | ||||||
chr20:32730930
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(205): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.85-2788A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32730930 | ||||||
chr20:32731147
|
T | C | 1 | a0001c0001t0002g0212 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.85-3005A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32731147 | ||||||
chr20:32731309
|
T | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(205): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.85-3167A>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32731309 | ||||||
chr20:32731313
|
A | G | 1 | a0001c0001t0002g0034 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.85-3171T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32731313 | ||||||
chr20:32731342
|
A | C | 1 | a0001c0001t0001g0363 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.85-3200T>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32731342 | ||||||
chr20:32731342
|
A | G | 206 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(203): Show | 225 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.85-3200T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32731342 | ||||||
chr20:32731400
|
G | A | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0135 | 3 | HG01891.hp1 HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.85-3258C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32731400 | ||||||
chr20:32731428
|
T | C | 4 | a0001c0001t0001g0036a0001c0001t0001g0059a0001c0001t0001g0060others(1): Show | 4 | NA18953.hp2 NA18980.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.85-3286A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32731428 | ||||||
chr20:32731571
|
C | A | 31 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0022others(28): Show | 33 | HG01167.hp2 HG01243.hp2 HG02040.hp2 others(30): Show |
intron_variant | MODIFIER | c.85-3429G>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32731571 | ||||||
chr20:32731792
|
G | C | 1 | a0001c0001t0002g0257 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.85-3650C>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32731792 | ||||||
chr20:32732034
|
A | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(205): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.85-3892T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32732034 | ||||||
chr20:32732121
|
C | T | 7 | a0001c0001t0003g0295a0001c0001t0003g0296a0001c0001t0003g0369others(4): Show | 7 | HG02630.hp1 HG02886.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.85-3979G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32732121 | ||||||
chr20:32732153
|
G | A | 135 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 151 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.85-4011C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32732153 | ||||||
chr20:32732156
|
C | T | 9 | a0001c0001t0001g0119a0001c0001t0001g0129a0001c0001t0001g0130others(6): Show | 9 | HG01891.hp1 HG02572.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.85-4014G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32732156 | ||||||
chr20:32732157
|
G | A | 1 | a0001c0001t0002g0253 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.85-4015C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32732157 | ||||||
chr20:32732198
|
C | T | 1 | a0001c0001t0009g0287 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.85-4056G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32732198 | ||||||
chr20:32732291
|
A | G | 1 | a0001c0001t0002g0334 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.85-4149T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32732291 | ||||||
chr20:32732296
|
G | T | 1 | a0001c0001t0001g0092 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.85-4154C>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32732296 | ||||||
chr20:32732354
|
G | T | 6 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0121others(3): Show | 9 | HG02451.hp1 HG02809.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.85-4212C>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32732354 | ||||||
chr20:32732390
|
C | A | 1 | a0001c0001t0002g0158 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.85-4248G>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32732390 | ||||||
chr20:32732390
|
C | T | 1 | a0001c0001t0002g0159 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.85-4248G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32732390 | ||||||
chr20:32732475
|
T | C | 3 | a0001c0001t0002g0017a0001c0001t0002g0213a0001c0001t0002g0214 | 4 | HG01255.hp1 HG01496.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.85-4333A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32732475 | ||||||
chr20:32732793
|
G | T | 1 | a0001c0001t0001g0106 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.85-4651C>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32732793 | ||||||
chr20:32732807
|
G | A | 1 | a0001c0001t0002g0223 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.85-4665C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32732807 | ||||||
chr20:32732829
|
G | A | 1 | a0001c0001t0002g0118 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.85-4687C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32732829 | ||||||
chr20:32732885
|
G | A | 3 | a0001c0001t0001g0109a0001c0001t0001g0286a0001c0001t0006g0120 | 3 | HG01109.hp2 HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.85-4743C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32732885 | ||||||
chr20:32732963
|
G | A | 1 | a0001c0001t0003g0295 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.85-4821C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32732963 | ||||||
chr20:32733293
|
A | G | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.85-5151T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32733293 | ||||||
chr20:32733305
|
G | C | 1 | a0001c0001t0001g0338 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.85-5163C>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32733305 | ||||||
chr20:32733351
|
C | T | 69 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(66): Show | 72 | HG00280.hp2 HG00741.hp2 HG01074.hp1 others(69): Show |
intron_variant | MODIFIER | c.85-5209G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32733351 | ||||||
chr20:32733417
|
T | C | 60 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(57): Show | 63 | HG00280.hp2 HG00741.hp2 HG01074.hp1 others(60): Show |
intron_variant | MODIFIER | c.85-5275A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32733417 | ||||||
chr20:32733678
|
T | C | 1 | a0001c0001t0001g0322 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.85-5536A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32733678 | ||||||
chr20:32733711
|
C | T | 69 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(66): Show | 72 | HG00280.hp2 HG00741.hp2 HG01074.hp1 others(69): Show |
intron_variant | MODIFIER | c.85-5569G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32733711 | ||||||
chr20:32733716
|
C | CA | 9 | a0001c0001t0001g0025a0001c0001t0001g0149a0001c0001t0001g0277others(6): Show | 9 | HG01346.hp2 HG01433.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.85-5575dupT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32733716 | ||||||
chr20:32733716
|
CA | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(184): Show | 202 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.85-5575delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32733716 | ||||||
chr20:32733716
|
CAA | C | 7 | a0001c0001t0001g0011a0001c0001t0001g0106a0001c0001t0001g0107others(4): Show | 8 | HG01256.hp2 HG01358.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.85-5576_85-5575del others(2): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32733716 | ||||||
chr20:32733867
|
G | C | 1 | a0001c0001t0002g0217 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.85-5725C>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32733867 | ||||||
chr20:32733934
|
T | G | 5 | a0001c0001t0001g0119a0001c0001t0001g0362a0001c0001t0001g0364others(2): Show | 5 | HG02572.hp1 HG02717.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.85-5792A>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32733934 | ||||||
chr20:32733944
|
C | T | 1 | a0001c0001t0001g0336 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.85-5802G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32733944 | ||||||
chr20:32733951
|
C | T | 8 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0072others(5): Show | 9 | HG01123.hp2 HG02257.hp2 HG03579.hp1 others(6): Show |
intron_variant | MODIFIER | c.85-5809G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32733951 | ||||||
chr20:32733991
|
C | T | 98 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(95): Show | 105 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.85-5849G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32733991 | ||||||
chr20:32734029
|
A | C | 1 | a0001c0001t0009g0287 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.85-5887T>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32734029 | ||||||
chr20:32734107
|
G | A | 4 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0148others(1): Show | 7 | HG02451.hp1 HG02809.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.85-5965C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32734107 | ||||||
chr20:32734113
|
A | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(205): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.85-5971T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32734113 | ||||||
chr20:32734131
|
A | C | 2 | a0001c0001t0002g0026a0001c0001t0002g0027 | 2 | HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.85-5989T>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32734131 | ||||||
chr20:32734161
|
A | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(205): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.85-6019T>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32734161 | ||||||
chr20:32734180
|
C | CA | 23 | a0001c0001t0001g0092a0001c0001t0001g0097a0001c0001t0001g0110others(20): Show | 24 | HG01261.hp1 HG01346.hp1 HG01928.hp2 others(21): Show |
intron_variant | MODIFIER | c.85-6039dupT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32734180 | ||||||
chr20:32734180
|
CA | C | 28 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(25): Show | 36 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.85-6039delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32734180 | ||||||
chr20:32734245
|
C | T | 2 | a0001c0001t0001g0311a0001c0001t0001g0313 | 2 | NA18970.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.85-6103G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32734245 | ||||||
chr20:32734466
|
C | T | 58 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(55): Show | 61 | HG00280.hp2 HG00741.hp2 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.85-6324G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32734466 | ||||||
chr20:32734467
|
G | A | 1 | a0001c0001t0001g0318 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.85-6325C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32734467 | ||||||
chr20:32734536
|
T | C | 1 | a0001c0001t0001g0319 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.85-6394A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32734536 | ||||||
chr20:32734548
|
A | T | 1 | a0001c0001t0001g0099 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.85-6406T>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32734548 | ||||||
chr20:32734748
|
T | C | 1 | a0001c0001t0005g0359 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.85-6606A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32734748 | ||||||
chr20:32734789
|
G | T | 3 | a0001c0001t0001g0116a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG02486.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.85-6647C>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32734789 | ||||||
chr20:32734816
|
C | T | 1 | a0001c0001t0001g0286 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.85-6674G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32734816 | ||||||
chr20:32734905
|
C | T | 3 | a0001c0001t0001g0067a0001c0001t0001g0070a0001c0001t0001g0071 | 3 | HG00733.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.85-6763G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32734905 | ||||||
chr20:32734924
|
AAAAAT | A | 4 | a0001c0001t0001g0025a0001c0001t0001g0277a0001c0001t0001g0278others(1): Show | 4 | HG01891.hp2 HG02145.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.85-6787_85-6783del others(5): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32734924 | ||||||
chr20:32735195
|
G | A | 1 | a0001c0001t0002g0262 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.85-7053C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32735195 | ||||||
chr20:32735231
|
CA | C | 8 | a0001c0001t0001g0040a0001c0001t0001g0137a0001c0001t0001g0138others(5): Show | 8 | HG00438.hp1 HG02135.hp1 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.85-7090delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32735231 | ||||||
chr20:32735243
|
AT | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(197): Show | 219 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.85-7102delA | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32735243 | ||||||
chr20:32735244
|
T | A | 159 | a0001c0001t0001g0053a0001c0001t0001g0116a0001c0001t0001g0133others(156): Show | 168 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.85-7102A>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32735244 | ||||||
chr20:32735253
|
A | G | 1 | a0001c0001t0001g0339 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.85-7111T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32735253 | ||||||
chr20:32735380
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.85-7238G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32735380 | ||||||
chr20:32735506
|
A | G | 1 | a0001c0001t0001g0266 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.85-7364T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32735506 | ||||||
chr20:32735566
|
C | T | 3 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0128 | 3 | HG02027.hp2 HG02056.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.85-7424G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32735566 | ||||||
chr20:32735598
|
T | C | 1 | a0001c0001t0001g0299 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.85-7456A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32735598 | ||||||
chr20:32735810
|
T | C | 1 | a0001c0001t0001g0146 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.84+7498A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32735810 | ||||||
chr20:32735843
|
A | G | 6 | a0001c0001t0001g0301a0001c0001t0001g0314a0001c0001t0001g0327others(3): Show | 6 | HG00741.hp2 HG01081.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.84+7465T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32735843 | ||||||
chr20:32736112
|
A | C | 211 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(208): Show | 230 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.84+7196T>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32736112 | ||||||
chr20:32736180
|
C | T | 360 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(357): Show | 385 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(382): Show |
intron_variant | MODIFIER | c.84+7128G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32736180 | ||||||
chr20:32736228
|
A | C | 211 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(208): Show | 230 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.84+7080T>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32736228 | ||||||
chr20:32736328
|
C | T | 206 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(203): Show | 225 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.84+6980G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32736328 | ||||||
chr20:32736339
|
A | T | 1 | a0001c0001t0002g0158 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.84+6969T>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32736339 | ||||||
chr20:32736354
|
G | A | 1 | a0001c0001t0001g0149 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.84+6954C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32736354 | ||||||
chr20:32736480
|
C | T | 9 | a0001c0001t0001g0119a0001c0001t0001g0129a0001c0001t0001g0130others(6): Show | 9 | HG01891.hp1 HG02572.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.84+6828G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32736480 | ||||||
chr20:32736487
|
G | A | 1 | a0001c0001t0002g0228 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.84+6821C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32736487 | ||||||
chr20:32736492
|
A | G | 1 | a0001c0001t0002g0105 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.84+6816T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32736492 | ||||||
chr20:32736626
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(205): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.84+6682A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32736626 | ||||||
chr20:32737368
|
T | A | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0135 | 3 | HG01891.hp1 HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.84+5940A>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32737368 | ||||||
chr20:32737379
|
A | AAAAAAAA others(12): Show |
1 | a0001c0001t0001g0323 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.84+5928_84+5929ins others(19): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32737379 | ||||||
chr20:32737379
|
A | AAAAAAAA others(11): Show |
21 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(18): Show | 27 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(24): Show |
intron_variant | MODIFIER | c.84+5928_84+5929ins others(18): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32737379 | ||||||
chr20:32737379
|
A | AAAAAAAA others(10): Show |
33 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(30): Show | 37 | HG00741.hp2 HG01358.hp2 HG02027.hp1 others(34): Show |
intron_variant | MODIFIER | c.84+5928_84+5929ins others(17): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32737379 | ||||||
chr20:32737379
|
A | AAAAAAAA others(9): Show |
137 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(134): Show | 146 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.84+5928_84+5929ins others(16): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32737379 | ||||||
chr20:32737379
|
A | AAAAAAAA others(8): Show |
15 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(12): Show | 15 | HG00280.hp2 HG01074.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.84+5928_84+5929ins others(15): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32737379 | ||||||
chr20:32737379
|
A | AAAAAAAA others(6): Show |
1 | a0001c0001t0002g0361 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.84+5928_84+5929ins others(13): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32737379 | ||||||
chr20:32737393
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.84+5915G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32737393 | ||||||
chr20:32737558
|
A | G | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 232 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.84+5750T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32737558 | ||||||
chr20:32737572
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(205): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.84+5736A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32737572 | ||||||
chr20:32737612
|
T | TA | 138 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(135): Show | 154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.84+5695dupT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32737612 | ||||||
chr20:32737665
|
TA | T | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 232 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.84+5642delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32737665 | ||||||
chr20:32737832
|
T | C | 1 | a0001c0001t0002g0229 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.84+5476A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32737832 | ||||||
chr20:32737837
|
T | TA | 6 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0136others(3): Show | 6 | HG01515.hp2 HG02258.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.84+5470dupT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32737837 | ||||||
chr20:32737837
|
T | TAA | 181 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(178): Show | 195 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.84+5469_84+5470dup others(2): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32737837 | ||||||
chr20:32737837
|
T | TAAA | 22 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(19): Show | 27 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(24): Show |
intron_variant | MODIFIER | c.84+5468_84+5470dup others(3): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32737837 | ||||||
chr20:32737837
|
TA | T | 6 | a0001c0001t0002g0013a0001c0001t0002g0034a0001c0001t0002g0152others(3): Show | 7 | HG01167.hp1 HG01169.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.84+5470delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32737837 | ||||||
chr20:32737947
|
TA | T | 211 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(208): Show | 231 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.84+5360delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32737947 | ||||||
chr20:32738025
|
A | G | 1 | a0001c0001t0002g0151 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.84+5283T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32738025 | ||||||
chr20:32738036
|
A | G | 3 | a0001c0001t0001g0116a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG02486.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.84+5272T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32738036 | ||||||
chr20:32738081
|
C | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(205): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.84+5227G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32738081 | ||||||
chr20:32738304
|
T | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(205): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.84+5004A>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32738304 | ||||||
chr20:32738364
|
A | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(205): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.84+4944T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32738364 | ||||||
chr20:32738423
|
T | A | 1 | a0001c0001t0001g0061 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.84+4885A>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32738423 | ||||||
chr20:32738478
|
T | C | 14 | a0001c0001t0001g0003a0001c0001t0001g0041a0001c0001t0001g0042others(11): Show | 16 | NA18946.hp2 NA18956.hp2 NA18960.hp2 others(13): Show |
intron_variant | MODIFIER | c.84+4830A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32738478 | ||||||
chr20:32738560
|
C | T | 1 | a0001c0001t0001g0066 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.84+4748G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32738560 | ||||||
chr20:32738969
|
C | G | 206 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(203): Show | 225 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.84+4339G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32738969 | ||||||
chr20:32739184
|
T | C | 5 | a0001c0001t0001g0025a0001c0001t0001g0277a0001c0001t0001g0278others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.84+4124A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739184 | ||||||
chr20:32739337
|
C | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(205): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.84+3971G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739337 | ||||||
chr20:32739369
|
G | C | 3 | a0001c0001t0001g0116a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG02486.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.84+3939C>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739369 | ||||||
chr20:32739451
|
C | A | 17 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(14): Show | 22 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(19): Show |
intron_variant | MODIFIER | c.84+3857G>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739451 | ||||||
chr20:32739525
|
C | G | 207 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(204): Show | 226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.84+3783G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739525 | ||||||
chr20:32739527
|
C | A | 3 | a0001c0001t0002g0231a0001c0001t0002g0232a0001c0001t0002g0233 | 3 | HG02129.hp1 NA18964.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.84+3781G>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739527 | ||||||
chr20:32739538
|
G | A | 1 | a0001c0001t0002g0283 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.84+3770C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739538 | ||||||
chr20:32739555
|
GAATGGCG others(665): Show |
G | 103 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(100): Show | 110 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.84+3081_84+3752del | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739555 | ||||||
chr20:32739628
|
G | C | 1 | a0001c0001t0002g0256 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.84+3680C>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739628 | ||||||
chr20:32739644
|
C | CA | 20 | a0001c0001t0001g0109a0001c0001t0002g0034a0001c0001t0002g0039others(17): Show | 20 | HG00408.hp2 HG00741.hp1 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.84+3663dupT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739644 | ||||||
chr20:32739644
|
C | CAAAAAA | 54 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(51): Show | 58 | HG00280.hp2 HG00733.hp2 HG01074.hp1 others(55): Show |
intron_variant | MODIFIER | c.84+3658_84+3663dup others(6): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739644 | ||||||
chr20:32739644
|
C | CAAAAAAA | 28 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0037others(25): Show | 31 | HG01081.hp2 HG01255.hp2 HG01358.hp2 others(28): Show |
intron_variant | MODIFIER | c.84+3657_84+3663dup others(7): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739644 | ||||||
chr20:32739644
|
C | CAAAAAAA others(2): Show |
12 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0125others(9): Show | 15 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.84+3655_84+3663dup others(9): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739644 | ||||||
chr20:32739644
|
C | CAAAAAAA others(3): Show |
5 | a0001c0001t0001g0006a0001c0001t0001g0320a0001c0001t0001g0321others(2): Show | 7 | HG00140.hp2 HG00735.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.84+3654_84+3663dup others(10): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739644 | ||||||
chr20:32739717
|
G | T | 1 | a0001c0001t0005g0359 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.84+3591C>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739717 | ||||||
chr20:32739748
|
T | G | 1 | a0001c0001t0003g0295 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.84+3560A>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739748 | ||||||
chr20:32739843
|
G | T | 107 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(104): Show | 119 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.84+3465C>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739843 | ||||||
chr20:32739878
|
T | C | 108 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(105): Show | 120 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.84+3430A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739878 | ||||||
chr20:32739879
|
G | A | 105 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(102): Show | 117 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.84+3429C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739879 | ||||||
chr20:32739926
|
G | A | 7 | a0001c0001t0001g0110a0001c0001t0001g0329a0001c0001t0001g0330others(4): Show | 7 | HG01258.hp2 HG01346.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.84+3382C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739926 | ||||||
chr20:32739949
|
T | C | 1 | a0001c0001t0003g0296 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.84+3359A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739949 | ||||||
chr20:32739969
|
C | T | 17 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(14): Show | 22 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(19): Show |
intron_variant | MODIFIER | c.84+3339G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739969 | ||||||
chr20:32739971
|
G | A | 2 | a0001c0001t0002g0244a0001c0001t0002g0285 | 2 | HG02922.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.84+3337C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739971 | ||||||
chr20:32739985
|
G | A | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(16): Show | 25 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(22): Show |
intron_variant | MODIFIER | c.84+3323C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32739985 | ||||||
chr20:32740067
|
C | G | 1 | a0001c0001t0002g0065 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.84+3241G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740067 | ||||||
chr20:32740114
|
G | A | 104 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(101): Show | 116 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.84+3194C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740114 | ||||||
chr20:32740184
|
G | A | 2 | a0001c0001t0001g0297a0001c0001t0001g0298 | 2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.84+3124C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740184 | ||||||
chr20:32740191
|
G | C | 106 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(103): Show | 118 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.84+3117C>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740191 | ||||||
chr20:32740233
|
C | T | 1 | a0001c0001t0002g0150 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.84+3075G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740233 | ||||||
chr20:32740242
|
G | A | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0135 | 3 | HG01891.hp1 HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.84+3066C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740242 | ||||||
chr20:32740272
|
A | G | 103 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(100): Show | 110 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.84+3036T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740272 | ||||||
chr20:32740316
|
CA | C | 207 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(204): Show | 226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.84+2991delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740316 | ||||||
chr20:32740364
|
G | A | 207 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(204): Show | 226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.84+2944C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740364 | ||||||
chr20:32740494
|
A | G | 3 | a0001c0001t0001g0116a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG02486.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.84+2814T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740494 | ||||||
chr20:32740542
|
TC | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(205): Show | 228 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.84+2765delG | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740542 | ||||||
chr20:32740556
|
G | A | 1 | a0001c0001t0001g0354 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.84+2752C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740556 | ||||||
chr20:32740562
|
G | A | 1 | a0001c0001t0001g0354 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.84+2746C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740562 | ||||||
chr20:32740575
|
G | A | 1 | a0001c0001t0008g0245 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.84+2733C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740575 | ||||||
chr20:32740620
|
T | A | 211 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(208): Show | 231 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.84+2688A>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740620 | ||||||
chr20:32740640
|
C | G | 1 | a0001c0001t0005g0359 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.84+2668G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740640 | ||||||
chr20:32740813
|
C | CA | 215 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(212): Show | 233 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.84+2494dupT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740813 | ||||||
chr20:32740813
|
C | CAA | 10 | a0001c0001t0001g0025a0001c0001t0001g0116a0001c0001t0001g0119others(7): Show | 11 | HG01884.hp2 HG02280.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.84+2493_84+2494dup others(2): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740813 | ||||||
chr20:32740873
|
T | A | 1 | a0001c0001t0001g0116 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.84+2435A>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740873 | ||||||
chr20:32740929
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.84+2379C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740929 | ||||||
chr20:32740969
|
G | C | 1 | a0001c0001t0001g0286 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.84+2339C>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740969 | ||||||
chr20:32740977
|
T | C | 6 | a0001c0001t0002g0257a0001c0001t0002g0258a0001c0001t0002g0259others(3): Show | 6 | HG01928.hp1 HG02132.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.84+2331A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740977 | ||||||
chr20:32740986
|
T | C | 65 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(62): Show | 71 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.84+2322A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32740986 | ||||||
chr20:32741105
|
T | C | 2 | a0001c0001t0001g0109a0001c0001t0001g0135 | 2 | HG01109.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.84+2203A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32741105 | ||||||
chr20:32741150
|
C | CA | 3 | a0001c0001t0001g0037a0001c0001t0001g0300a0001c0001t0001g0371 | 3 | HG00741.hp2 HG02027.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.84+2157dupT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32741150 | ||||||
chr20:32741154
|
C | A | 38 | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0037others(35): Show | 39 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.84+2154G>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32741154 | ||||||
chr20:32741158
|
C | A | 69 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0033others(66): Show | 71 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(68): Show |
intron_variant | MODIFIER | c.84+2150G>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32741158 | ||||||
chr20:32741158
|
CA | C | 149 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(146): Show | 166 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.84+2149delT | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32741158 | ||||||
chr20:32741209
|
A | T | 12 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(9): Show | 12 | HG01884.hp2 HG01891.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.84+2099T>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32741209 | ||||||
chr20:32741259
|
T | C | 1 | a0001c0001t0001g0368 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.84+2049A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32741259 | ||||||
chr20:32741377
|
G | A | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | HG02486.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.84+1931C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32741377 | ||||||
chr20:32741388
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.84+1920C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32741388 | ||||||
chr20:32741395
|
G | GT | 197 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(194): Show | 213 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.84+1912dupA | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32741395 | ||||||
chr20:32741395
|
G | GTT | 14 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(11): Show | 14 | HG01884.hp2 HG02027.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.84+1911_84+1912dup others(2): Show |
COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32741395 | ||||||
chr20:32741450
|
G | A | 71 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0024others(68): Show | 77 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.84+1858C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32741450 | ||||||
chr20:32741596
|
G | A | 1 | a0001c0001t0002g0112 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.84+1712C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32741596 | ||||||
chr20:32741597
|
G | C | 1 | a0001c0001t0009g0287 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.84+1711C>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32741597 | ||||||
chr20:32741630
|
C | G | 3 | a0001c0001t0002g0113a0001c0001t0002g0114a0001c0001t0002g0115 | 3 | HG02647.hp1 HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.84+1678G>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32741630 | ||||||
chr20:32741657
|
A | G | 2 | a0001c0001t0002g0111a0001c0001t0002g0112 | 2 | HG00099.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.84+1651T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32741657 | ||||||
chr20:32741898
|
A | G | 71 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0019others(68): Show | 76 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.84+1410T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32741898 | ||||||
chr20:32741964
|
G | A | 1 | a0001c0001t0001g0370 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.84+1344C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32741964 | ||||||
chr20:32742060
|
T | C | 1 | a0001c0001t0001g0371 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.84+1248A>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32742060 | ||||||
chr20:32742136
|
G | A | 1 | a0001c0001t0002g0280 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.84+1172C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32742136 | ||||||
chr20:32742143
|
C | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(74): Show | 86 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.84+1165G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32742143 | ||||||
chr20:32742309
|
C | T | 294 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(291): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.84+999G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32742309 | ||||||
chr20:32742369
|
G | C | 1 | a0001c0001t0002g0283 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.84+939C>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32742369 | ||||||
chr20:32742462
|
A | G | 1 | a0001c0001t0001g0025 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.84+846T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32742462 | ||||||
chr20:32742529
|
G | A | 4 | a0001c0001t0001g0286a0001c0001t0002g0284a0001c0001t0002g0285others(1): Show | 4 | HG00741.hp1 HG02572.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.84+779C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32742529 | ||||||
chr20:32742546
|
C | A | 1 | a0001c0001t0002g0288 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.84+762G>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32742546 | ||||||
chr20:32742551
|
G | C | 10 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0002g0289others(7): Show | 10 | HG02055.hp2 HG02451.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.84+757C>G | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32742551 | ||||||
chr20:32742554
|
G | A | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0024others(1): Show | 4 | HG01167.hp2 HG01243.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.84+754C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32742554 | ||||||
chr20:32742555
|
G | A | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0024others(1): Show | 4 | HG01167.hp2 HG01243.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.84+753C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32742555 | ||||||
chr20:32742607
|
G | A | 295 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(292): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.84+701C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32742607 | ||||||
chr20:32742806
|
A | G | 296 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(293): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.84+502T>C | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32742806 | ||||||
chr20:32742940
|
C | T | 10 | a0001c0001t0001g0025a0001c0001t0001g0033a0001c0001t0002g0026others(7): Show | 11 | HG01361.hp2 HG02280.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.84+368G>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32742940 | ||||||
chr20:32743085
|
G | T | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0024others(1): Show | 4 | HG01167.hp2 HG01243.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.84+223C>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32743085 | ||||||
chr20:32743224
|
G | T | 1 | a0001c0001t0002g0020 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.84+84C>A | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32743224 | ||||||
chr20:32743280
|
G | A | 1 | a0001c0001t0001g0372 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.84+28C>T | COMMD7 | ENSG00000149600.12 | transcript | ENST00000278980.11 | protein_coding | 1/8 | chr20 | 32743280 |