geneid | 137682 |
---|---|
ensemblid | ENSG00000156170.14 |
hgncid | 28625 |
symbol | NDUFAF6 |
name | NADH:ubiquinone oxidoreductase complex assembly factor 6 |
refseq_nuc | NM_152416.4 |
refseq_prot | NP_689629.2 |
ensembl_nuc | ENST00000396124.9 |
ensembl_prot | ENSP00000379430.4 |
mane_status | MANE Select |
chr | chr8 |
start | 95024989 |
end | 95058710 |
strand | + |
ver | v1.2 |
region | chr8:95024989-95058710 |
region5000 | chr8:95019989-95063710 |
regionname0 | NDUFAF6_chr8_95024989_95058710 |
regionname5000 | NDUFAF6_chr8_95019989_95063710 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 333 | 335 | 92 | 66 | 134 | 12 | 29 | 98 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | copy fasta | chr8 | 95019989 | 95063710 |
a0002 | 0/0 | 333 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | copy fasta | chr8 | 95019989 | 95063710 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1002 | 328 | 86 | 65 | 134 | 12 | 29 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | copy fasta | chr8 | 95019989 | 95063710 |
c0002 | 0/0 | 1002 | 3 | 3 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | copy fasta | chr8 | 95019989 | 95063710 |
c0003 | 0/0 | 1002 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | copy fasta | chr8 | 95019989 | 95063710 |
c0004 | 0/0 | 1002 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | copy fasta | chr8 | 95019989 | 95063710 |
c0005 | 0/0 | 1002 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | copy fasta | chr8 | 95019989 | 95063710 |
c0006 | 0/0 | 1002 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | copy fasta | chr8 | 95019989 | 95063710 |
c0007 | 0/0 | 1002 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | copy fasta | chr8 | 95019989 | 95063710 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 794 | 301 | 64 | 62 | 134 | 11 | 29 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | copy fasta | chr8 | 95019989 | 95063710 |
t0002 | 1/0 | 794 | 10 | 5 | 3 | 0 | 1 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | copy fasta | chr8 | 95019989 | 95063710 |
t0003 | 0/0 | 794 | 9 | 9 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | copy fasta | chr8 | 95019989 | 95063710 |
t0004 | 0/0 | 794 | 8 | 7 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | copy fasta | chr8 | 95019989 | 95063710 |
t0005 | 0/0 | 794 | 3 | 3 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | copy fasta | chr8 | 95019989 | 95063710 |
t0006 | 0/0 | 794 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | copy fasta | chr8 | 95019989 | 95063710 |
t0007 | 0/0 | 794 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | copy fasta | chr8 | 95019989 | 95063710 |
t0008 | 0/0 | 794 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | copy fasta | chr8 | 95019989 | 95063710 |
t0009 | 0/0 | 794 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | copy fasta | chr8 | 95019989 | 95063710 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 28 | 1 | 3 | 18 | 3 | 3 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0002 | 0/0 | 18 | 0 | 5 | 11 | 0 | 2 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0003 | 0/0 | 8 | 1 | 1 | 5 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0004 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0005 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0007 | 0/0 | 6 | 1 | 4 | 0 | 1 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0008 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0009 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0010 | 0/0 | 5 | 1 | 2 | 2 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0011 | 0/0 | 4 | 0 | 0 | 1 | 1 | 2 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0015 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0037 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0057 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0135 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1002 | 328 | 86 | 65 | 134 | 12 | 29 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | copy fasta | chr8 | 95019989 | 95063710 |
a0001c0002 | 0/0 | 1002 | 3 | 3 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | copy fasta | chr8 | 95019989 | 95063710 |
a0001c0003 | 0/0 | 1002 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | copy fasta | chr8 | 95019989 | 95063710 |
a0001c0005 | 0/0 | 1002 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | copy fasta | chr8 | 95019989 | 95063710 |
a0001c0006 | 0/0 | 1002 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | copy fasta | chr8 | 95019989 | 95063710 |
a0001c0007 | 0/0 | 1002 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | copy fasta | chr8 | 95019989 | 95063710 |
a0002c0004 | 0/0 | 1002 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | copy fasta | chr8 | 95019989 | 95063710 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 1795 | 299 | 63 | 62 | 134 | 11 | 28 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | copy fasta | chr8 | 95019989 | 95063710 |
a0001c0001t0002 | 1/0 | 1795 | 9 | 4 | 3 | 0 | 1 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | copy fasta | chr8 | 95019989 | 95063710 |
a0001c0001t0003 | 0/0 | 1795 | 9 | 9 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | copy fasta | chr8 | 95019989 | 95063710 |
a0001c0001t0004 | 0/0 | 1795 | 7 | 7 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | copy fasta | chr8 | 95019989 | 95063710 |
a0001c0001t0006 | 0/0 | 1795 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | copy fasta | chr8 | 95019989 | 95063710 |
a0001c0001t0007 | 0/0 | 1795 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | copy fasta | chr8 | 95019989 | 95063710 |
a0001c0001t0009 | 0/0 | 1795 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | copy fasta | chr8 | 95019989 | 95063710 |
a0001c0002t0005 | 0/0 | 1795 | 3 | 3 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | copy fasta | chr8 | 95019989 | 95063710 |
a0001c0003t0008 | 0/0 | 1795 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | copy fasta | chr8 | 95019989 | 95063710 |
a0001c0005t0001 | 0/0 | 1795 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | copy fasta | chr8 | 95019989 | 95063710 |
a0001c0006t0004 | 0/0 | 1795 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | copy fasta | chr8 | 95019989 | 95063710 |
a0001c0007t0002 | 0/0 | 1795 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | copy fasta | chr8 | 95019989 | 95063710 |
a0002c0004t0001 | 0/0 | 1795 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | copy fasta | chr8 | 95019989 | 95063710 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 26 | 1 | 3 | 18 | 3 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0002 | 0/0 | 18 | 0 | 5 | 11 | 0 | 2 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0003 | 0/0 | 8 | 1 | 1 | 5 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0004 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0005 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0007 | 0/0 | 6 | 1 | 4 | 0 | 1 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0008 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0009 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0010 | 0/0 | 5 | 1 | 2 | 2 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 1 | 1 | 2 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0057 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0002g0135 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0003g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0006g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0007g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0001t0009g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0002t0005g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0002t0005g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0002t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0003t0008g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0005t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0006t0004g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0001c0007t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
a0002c0004t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | GBR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0133 | EUR | GBR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0091 | EUR | GBR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01261 | hp1 | a0001 | c0006 | t0004 | g0070 | AMR | CLM | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0131 | AMR | CLM | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | ACB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0132 | AMR | PEL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0125 | AFR | ACB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CDX | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CDX | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CDX | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02257 | hp1 | a0001 | c0002 | t0005 | g0076 | AFR | ACB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0126 | AFR | ACB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0062 | AFR | ACB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0047 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02717 | hp2 | a0001 | c0001 | t0004 | g0046 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0039 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02818 | hp2 | a0001 | c0001 | t0007 | g0048 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0063 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0124 | AFR | ESN | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02976 | hp1 | a0001 | c0002 | t0005 | g0077 | AFR | ESN | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ESN | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03041 | hp1 | a0001 | c0001 | t0006 | g0028 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03098 | hp1 | a0001 | c0007 | t0002 | g0128 | AFR | MSL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | MSL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03486 | hp1 | a0001 | c0001 | t0004 | g0074 | AFR | MSL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03486 | hp2 | a0001 | c0001 | t0006 | g0028 | AFR | MSL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0122 | AFR | ESN | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03516 | hp2 | a0001 | c0001 | t0004 | g0073 | AFR | ESN | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03540 | hp1 | a0001 | c0002 | t0005 | g0075 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | STU | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | STU | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03710 | hp1 | a0001 | c0001 | t0009 | g0001 | SAS | PJL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03831 | hp1 | a0002 | c0004 | t0001 | g0001 | SAS | BEB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | BEB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | BEB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | BEB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | STU | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | STU | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | BEB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | STU | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | STU | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | YRI | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | YRI | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | CHB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0123 | AFR | YRI | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA19240 | hp2 | a0001 | c0003 | t0008 | g0052 | AFR | YRI | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0127 | AFR | ASW | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ASW | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0183 | EUR | TSI | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0065 | EUR | TSI | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0056 | EUR | TSI | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | GIH | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | GIH | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0129 | AFR | MSL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | USA | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
HG06807 | hp2 | a0001 | c0005 | t0001 | g0141 | AFR | USA | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | USA | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | USA | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | LWK | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0057 | REF | REF | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0135 | REF | REF | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:95025091
|
G | C | 1 | a0002 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.83G>C | p.Gly28Ala | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/9 | 103/1795 | 83/1002 | 28/333 | chr8 | 95025091 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:95025059
|
C | A | 1 | a0001c0003 | 1 | NA19240.hp2 | synonymous_variant | LOW | c.51C>A | p.Ile17Ile | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/9 | 71/1795 | 51/1002 | 17/333 | chr8 | 95025059 | ||
chr8:95032019
|
A | G | 1 | a0001c0007 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.222A>G | p.Leu74Leu | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/9 | 242/1795 | 222/1002 | 74/333 | chr8 | 95032019 | ||
chr8:95032022
|
C | T | 1 | a0001c0002 | 3 | HG02257.hp1 HG02976.hp1 HG03540.hp1 |
synonymous_variant | LOW | c.225C>T | p.Cys75Cys | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/9 | 245/1795 | 225/1002 | 75/333 | chr8 | 95032022 | ||
chr8:95047055
|
C | T | 1 | a0001c0006 | 1 | HG01261.hp1 | synonymous_variant | LOW | c.642C>T | p.Val214Val | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/9 | 662/1795 | 642/1002 | 214/333 | chr8 | 95047055 | ||
chr8:95052209
|
A | C | 1 | a0001c0005 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.852A>C | p.Ala284Ala | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/9 | 872/1795 | 852/1002 | 284/333 | chr8 | 95052209 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:95057953
|
T | C | 10 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(7): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(314): Show |
3_prime_UTR_variant | MODIFIER | c.*16T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 9/9 | 16 | chr8 | 95057953 | |||||
chr8:95058081
|
T | G | 1 | a0001c0001t0007 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*144T>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 9/9 | 144 | chr8 | 95058081 | |||||
chr8:95058086
|
G | A | 1 | a0001c0001t0006 | 2 | HG03041.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*149G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 9/9 | 149 | chr8 | 95058086 | |||||
chr8:95058145
|
T | C | 5 | a0001c0001t0004a0001c0001t0007a0001c0002t0005others(2): Show | 13 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*208T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 9/9 | 208 | chr8 | 95058145 | |||||
chr8:95058246
|
G | A | 1 | a0001c0001t0003 | 9 | HG02145.hp2 HG02257.hp2 HG02622.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*309G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 9/9 | 309 | chr8 | 95058246 | |||||
chr8:95058258
|
G | A | 1 | a0001c0003t0008 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*321G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 9/9 | 321 | chr8 | 95058258 | |||||
chr8:95058325
|
C | G | 1 | a0001c0001t0009 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*388C>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 9/9 | 388 | chr8 | 95058325 | |||||
chr8:95058645
|
G | C | 5 | a0001c0001t0004a0001c0001t0007a0001c0002t0005others(2): Show | 13 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*708G>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 9/9 | 708 | chr8 | 95058645 | |||||
chr8:95058687
|
C | T | 1 | a0001c0002t0005 | 3 | HG02257.hp1 HG02976.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*750C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 9/9 | 750 | chr8 | 95058687 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:95025248
|
CCCGGGGT others(8): Show |
C | 1 | a0001c0001t0001g0206 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.197+45_197+59delCG others(13): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr8 | 95025248 | |||||
chr8:95025519
|
T | A | 1 | a0001c0001t0001g0020 | 2 | HG01255.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.197+314T>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95025519 | ||||||
chr8:95025540
|
A | G | 1 | a0001c0001t0001g0205 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.197+335A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95025540 | ||||||
chr8:95025637
|
T | A | 1 | a0001c0001t0001g0043 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.197+432T>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95025637 | ||||||
chr8:95025784
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.197+579C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95025784 | ||||||
chr8:95025844
|
G | A | 30 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0021others(27): Show | 38 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.197+639G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95025844 | ||||||
chr8:95026024
|
C | G | 97 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(94): Show | 170 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(167): Show |
intron_variant | MODIFIER | c.197+819C>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95026024 | ||||||
chr8:95026239
|
C | G | 1 | a0001c0001t0001g0069 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.197+1034C>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95026239 | ||||||
chr8:95026245
|
G | A | 190 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(187): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.197+1040G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95026245 | ||||||
chr8:95026338
|
C | T | 5 | a0001c0001t0001g0019a0001c0001t0001g0042a0001c0001t0001g0201others(2): Show | 8 | HG00621.hp1 HG02040.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.197+1133C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95026338 | ||||||
chr8:95026492
|
T | G | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG03831.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.197+1287T>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95026492 | ||||||
chr8:95026591
|
G | T | 3 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068 | 3 | HG01891.hp2 HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.197+1386G>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95026591 | ||||||
chr8:95026623
|
T | C | 1 | a0001c0006t0004g0070 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.197+1418T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95026623 | ||||||
chr8:95026731
|
T | C | 30 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0021others(27): Show | 38 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.197+1526T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95026731 | ||||||
chr8:95026880
|
G | C | 1 | a0001c0001t0001g0022 | 2 | HG01070.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.197+1675G>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95026880 | ||||||
chr8:95026915
|
G | A | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | HG02027.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.197+1710G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95026915 | ||||||
chr8:95026948
|
A | AG | 27 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0021others(24): Show | 35 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.197+1745dupG | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr8 | 95026948 | |||||
chr8:95026988
|
A | C | 1 | a0001c0001t0001g0065 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.197+1783A>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95026988 | ||||||
chr8:95026995
|
G | A | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG02109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.197+1790G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95026995 | ||||||
chr8:95027019
|
T | C | 30 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0021others(27): Show | 38 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.197+1814T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95027019 | ||||||
chr8:95027158
|
C | T | 1 | a0001c0001t0007g0048 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.197+1953C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95027158 | ||||||
chr8:95027163
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.197+1958C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95027163 | ||||||
chr8:95027269
|
T | C | 5 | a0001c0001t0004g0073a0001c0001t0004g0074a0001c0002t0005g0075others(2): Show | 5 | HG02257.hp1 HG02976.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.197+2064T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95027269 | ||||||
chr8:95027579
|
C | CA | 28 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0021others(25): Show | 36 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.197+2393dupA | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr8 | 95027579 | |||||
chr8:95027579
|
C | CAA | 7 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0050others(4): Show | 7 | HG01891.hp2 HG01981.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.197+2392_197+2393d others(4): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr8 | 95027579 | |||||
chr8:95027579
|
CA | C | 7 | a0001c0001t0001g0041a0001c0001t0001g0119a0001c0001t0001g0120others(4): Show | 8 | HG03710.hp2 NA18981.hp1 NA18986.hp2 others(5): Show |
intron_variant | MODIFIER | c.197+2393delA | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr8 | 95027579 | |||||
chr8:95027712
|
A | T | 1 | a0001c0001t0004g0063 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.197+2507A>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95027712 | ||||||
chr8:95027866
|
C | T | 2 | a0001c0001t0004g0046a0001c0001t0004g0047 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.197+2661C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95027866 | ||||||
chr8:95028229
|
T | C | 1 | a0001c0001t0001g0051 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.197+3024T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95028229 | ||||||
chr8:95028489
|
T | C | 1 | a0001c0001t0001g0013 | 3 | HG02080.hp2 HG02523.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.197+3284T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95028489 | ||||||
chr8:95028659
|
A | G | 31 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0021others(28): Show | 39 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.198-3336A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95028659 | ||||||
chr8:95028804
|
A | G | 7 | a0001c0001t0001g0026a0001c0001t0001g0113a0001c0001t0001g0114others(4): Show | 8 | HG00438.hp1 HG02155.hp1 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.198-3191A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95028804 | ||||||
chr8:95028967
|
C | A | 1 | a0001c0005t0001g0141 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.198-3028C>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95028967 | ||||||
chr8:95029022
|
G | A | 30 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0021others(27): Show | 38 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.198-2973G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95029022 | ||||||
chr8:95029039
|
A | G | 190 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(187): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.198-2956A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95029039 | ||||||
chr8:95029132
|
A | C | 2 | a0001c0001t0001g0040a0001c0001t0001g0195 | 3 | HG03654.hp2 HG03927.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.198-2863A>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95029132 | ||||||
chr8:95029209
|
G | A | 30 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0021others(27): Show | 38 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.198-2786G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95029209 | ||||||
chr8:95029262
|
T | C | 2 | a0001c0001t0004g0046a0001c0001t0004g0047 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.198-2733T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95029262 | ||||||
chr8:95029372
|
AT | A | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(201): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.198-2617delT | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr8 | 95029372 | |||||
chr8:95029416
|
A | G | 21 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0013others(18): Show | 46 | HG00609.hp2 HG00639.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.198-2579A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95029416 | ||||||
chr8:95029518
|
T | C | 30 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0021others(27): Show | 38 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.198-2477T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95029518 | ||||||
chr8:95029556
|
A | C | 1 | a0001c0001t0001g0068 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.198-2439A>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95029556 | ||||||
chr8:95029606
|
C | T | 5 | a0001c0001t0004g0073a0001c0001t0004g0074a0001c0002t0005g0075others(2): Show | 5 | HG02257.hp1 HG02976.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.198-2389C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95029606 | ||||||
chr8:95029954
|
G | A | 2 | a0001c0001t0004g0046a0001c0001t0004g0047 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.198-2041G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95029954 | ||||||
chr8:95030214
|
A | ATTAT | 10 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0099others(7): Show | 16 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.198-1754_198-1751d others(6): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr8 | 95030214 | |||||
chr8:95030214
|
A | ATTATTTA others(9): Show |
2 | a0001c0001t0004g0046a0001c0001t0004g0047 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.198-1766_198-1751d others(18): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr8 | 95030214 | |||||
chr8:95030314
|
C | T | 1 | a0001c0006t0004g0070 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.198-1681C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95030314 | ||||||
chr8:95030535
|
T | C | 3 | a0001c0001t0001g0051a0001c0001t0001g0053a0001c0001t0001g0054 | 3 | HG02280.hp2 HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.198-1460T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95030535 | ||||||
chr8:95030662
|
A | G | 30 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0021others(27): Show | 38 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.198-1333A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95030662 | ||||||
chr8:95030960
|
A | G | 30 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0021others(27): Show | 38 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.198-1035A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95030960 | ||||||
chr8:95030993
|
T | G | 5 | a0001c0001t0004g0073a0001c0001t0004g0074a0001c0002t0005g0075others(2): Show | 5 | HG02257.hp1 HG02976.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.198-1002T>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95030993 | ||||||
chr8:95031020
|
T | C | 1 | a0001c0001t0001g0205 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.198-975T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95031020 | ||||||
chr8:95031148
|
G | A | 1 | a0001c0001t0001g0142 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.198-847G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95031148 | ||||||
chr8:95031151
|
C | G | 1 | a0001c0006t0004g0070 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.198-844C>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95031151 | ||||||
chr8:95031371
|
C | T | 6 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(3): Show | 6 | HG01891.hp2 HG02258.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.198-624C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95031371 | ||||||
chr8:95031414
|
T | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(205): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.198-581T>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95031414 | ||||||
chr8:95031474
|
A | T | 1 | a0001c0001t0001g0068 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.198-521A>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95031474 | ||||||
chr8:95031487
|
A | C | 1 | a0001c0001t0001g0194 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.198-508A>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95031487 | ||||||
chr8:95031552
|
G | A | 5 | a0001c0001t0001g0029a0001c0001t0001g0143a0001c0001t0001g0144others(2): Show | 6 | HG00642.hp1 HG01168.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.198-443G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95031552 | ||||||
chr8:95031601
|
G | A | 30 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0021others(27): Show | 38 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.198-394G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95031601 | ||||||
chr8:95031712
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.198-283G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95031712 | ||||||
chr8:95031814
|
T | C | 27 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0021others(24): Show | 35 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.198-181T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95031814 | ||||||
chr8:95031820
|
C | CG | 5 | a0001c0001t0004g0073a0001c0001t0004g0074a0001c0002t0005g0075others(2): Show | 5 | HG02257.hp1 HG02976.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.198-174dupG | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr8 | 95031820 | |||||
chr8:95031838
|
T | C | 1 | a0001c0001t0004g0074 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.198-157T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95031838 | ||||||
chr8:95031848
|
G | A | 21 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0021others(18): Show | 29 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.198-147G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95031848 | ||||||
chr8:95031876
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.198-119C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95031876 | ||||||
chr8:95031880
|
C | T | 1 | a0001c0001t0001g0112 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.198-115C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95031880 | ||||||
chr8:95031892
|
C | T | 1 | a0001c0001t0007g0048 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.198-103C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95031892 | ||||||
chr8:95031893
|
G | A | 4 | a0001c0001t0001g0148a0001c0001t0004g0062a0001c0001t0004g0063others(1): Show | 4 | HG02258.hp1 HG02886.hp1 NA19087.hp2 others(1): Show |
intron_variant | MODIFIER | c.198-102G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95031893 | ||||||
chr8:95032155
|
T | A | 2 | a0001c0001t0001g0040a0001c0001t0001g0195 | 3 | HG03654.hp2 HG03927.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.297+61T>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95032155 | ||||||
chr8:95032186
|
A | T | 5 | a0001c0001t0004g0073a0001c0001t0004g0074a0001c0002t0005g0075others(2): Show | 5 | HG02257.hp1 HG02976.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.297+92A>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95032186 | ||||||
chr8:95032739
|
A | C | 27 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0021others(24): Show | 35 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.297+645A>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95032739 | ||||||
chr8:95032841
|
A | G | 3 | a0001c0001t0002g0129a0001c0001t0002g0130a0001c0001t0006g0028 | 4 | HG01884.hp1 HG03041.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.297+747A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95032841 | ||||||
chr8:95032909
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.297+815C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95032909 | ||||||
chr8:95033171
|
T | C | 21 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0021others(18): Show | 29 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.297+1077T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95033171 | ||||||
chr8:95033213
|
A | C | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(186): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.297+1119A>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95033213 | ||||||
chr8:95033235
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.297+1141G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95033235 | ||||||
chr8:95033245
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.297+1151A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95033245 | ||||||
chr8:95033332
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.297+1238C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95033332 | ||||||
chr8:95033341
|
G | C | 58 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(55): Show | 97 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.297+1247G>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95033341 | ||||||
chr8:95033354
|
T | G | 2 | a0001c0001t0004g0046a0001c0001t0004g0047 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.297+1260T>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95033354 | ||||||
chr8:95033725
|
G | T | 1 | a0001c0001t0001g0192 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.297+1631G>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95033725 | ||||||
chr8:95033784
|
G | A | 3 | a0001c0001t0001g0138a0001c0001t0001g0152a0001c0001t0001g0153 | 3 | HG02965.hp1 HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.298-1670G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95033784 | ||||||
chr8:95033866
|
G | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 266 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.298-1588G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95033866 | ||||||
chr8:95034140
|
A | G | 1 | a0001c0006t0004g0070 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.298-1314A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95034140 | ||||||
chr8:95034261
|
T | C | 1 | a0001c0006t0004g0070 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.298-1193T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95034261 | ||||||
chr8:95034265
|
G | A | 5 | a0001c0001t0004g0073a0001c0001t0004g0074a0001c0002t0005g0075others(2): Show | 5 | HG02257.hp1 HG02976.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.298-1189G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95034265 | ||||||
chr8:95034265
|
G | C | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 266 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.298-1189G>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95034265 | ||||||
chr8:95034405
|
C | G | 3 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0003t0008g0052 | 3 | HG02258.hp1 HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.298-1049C>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95034405 | ||||||
chr8:95034458
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.298-996G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95034458 | ||||||
chr8:95034459
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.298-995G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95034459 | ||||||
chr8:95034625
|
T | C | 1 | a0001c0001t0001g0155 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.298-829T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95034625 | ||||||
chr8:95034650
|
G | A | 1 | a0001c0001t0001g0113 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.298-804G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95034650 | ||||||
chr8:95034654
|
T | C | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0194 | 5 | HG02486.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.298-800T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95034654 | ||||||
chr8:95034694
|
A | T | 2 | a0001c0001t0004g0046a0001c0001t0004g0047 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.298-760A>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95034694 | ||||||
chr8:95034723
|
A | G | 21 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0021others(18): Show | 29 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.298-731A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95034723 | ||||||
chr8:95034823
|
C | A | 1 | a0001c0001t0001g0100 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.298-631C>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95034823 | ||||||
chr8:95034825
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.298-629A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95034825 | ||||||
chr8:95034839
|
G | C | 5 | a0001c0001t0004g0073a0001c0001t0004g0074a0001c0002t0005g0075others(2): Show | 5 | HG02257.hp1 HG02976.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.298-615G>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95034839 | ||||||
chr8:95034967
|
C | T | 4 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0003t0008g0052others(1): Show | 4 | HG01261.hp1 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.298-487C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95034967 | ||||||
chr8:95035020
|
C | G | 3 | a0001c0002t0005g0075a0001c0002t0005g0076a0001c0002t0005g0077 | 3 | HG02257.hp1 HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.298-434C>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95035020 | ||||||
chr8:95035040
|
C | T | 8 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0073others(5): Show | 8 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.298-414C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95035040 | ||||||
chr8:95035069
|
C | T | 4 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0003t0008g0052others(1): Show | 4 | HG01261.hp1 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.298-385C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95035069 | ||||||
chr8:95035081
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.298-373A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95035081 | ||||||
chr8:95035242
|
CTT | C | 21 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0021others(18): Show | 29 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.298-211_298-210del others(2): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95035242 | ||||||
chr8:95035380
|
A | G | 8 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0073others(5): Show | 8 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.298-74A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95035380 | ||||||
chr8:95035393
|
G | C | 21 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0021others(18): Show | 29 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.298-61G>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95035393 | ||||||
chr8:95035578
|
T | TA | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(188): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.420+15dupA | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 95035578 | |||||
chr8:95035578
|
T | TAA | 14 | a0001c0001t0001g0071a0001c0001t0001g0148a0001c0001t0001g0156others(11): Show | 14 | HG01081.hp1 HG02027.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.420+14_420+15dupAA | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 95035578 | |||||
chr8:95035655
|
T | G | 2 | a0001c0001t0004g0046a0001c0001t0004g0047 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.420+79T>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95035655 | ||||||
chr8:95035705
|
C | G | 21 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0021others(18): Show | 29 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.420+129C>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95035705 | ||||||
chr8:95035880
|
A | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0191 | 4 | HG00642.hp2 HG01074.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.420+304A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95035880 | ||||||
chr8:95035906
|
TCTGCCTA others(7): Show |
T | 4 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0003t0008g0052others(1): Show | 4 | HG01261.hp1 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.420+333_420+346del others(14): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 95035906 | |||||
chr8:95036541
|
A | G | 1 | a0001c0006t0004g0070 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.420+965A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95036541 | ||||||
chr8:95036609
|
C | T | 1 | a0001c0001t0001g0025 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.420+1033C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95036609 | ||||||
chr8:95036618
|
C | T | 8 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0073others(5): Show | 8 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.420+1042C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95036618 | ||||||
chr8:95036689
|
T | G | 4 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0003t0008g0052others(1): Show | 4 | HG01261.hp1 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.420+1113T>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95036689 | ||||||
chr8:95036712
|
T | C | 11 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(8): Show | 11 | HG01891.hp2 HG02257.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.420+1136T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95036712 | ||||||
chr8:95036805
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.420+1229A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95036805 | ||||||
chr8:95036838
|
T | C | 4 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0003t0008g0052others(1): Show | 4 | HG01261.hp1 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.420+1262T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95036838 | ||||||
chr8:95036892
|
A | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.420+1316A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95036892 | ||||||
chr8:95036948
|
C | T | 5 | a0001c0001t0004g0073a0001c0001t0004g0074a0001c0002t0005g0075others(2): Show | 5 | HG02257.hp1 HG02976.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.420+1372C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95036948 | ||||||
chr8:95037014
|
T | G | 4 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0003t0008g0052others(1): Show | 4 | HG01261.hp1 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.420+1438T>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95037014 | ||||||
chr8:95037111
|
T | C | 60 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(57): Show | 99 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.420+1535T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95037111 | ||||||
chr8:95037329
|
C | T | 3 | a0001c0001t0001g0039a0001c0001t0001g0190a0001c0001t0004g0039 | 3 | HG01081.hp2 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.420+1753C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95037329 | ||||||
chr8:95037369
|
T | C | 1 | a0001c0001t0007g0048 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.420+1793T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95037369 | ||||||
chr8:95037456
|
C | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 266 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.420+1880C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95037456 | ||||||
chr8:95037550
|
C | G | 3 | a0001c0001t0001g0041a0001c0001t0001g0198a0001c0001t0001g0199 | 4 | NA18981.hp1 NA18999.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.420+1974C>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95037550 | ||||||
chr8:95037656
|
C | T | 8 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0073others(5): Show | 8 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.420+2080C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95037656 | ||||||
chr8:95037774
|
G | A | 12 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0062others(9): Show | 12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.420+2198G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95037774 | ||||||
chr8:95037896
|
A | G | 1 | a0001c0001t0001g0189 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.420+2320A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95037896 | ||||||
chr8:95038032
|
C | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0199 | 3 | NA18981.hp1 NA18999.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.420+2456C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95038032 | ||||||
chr8:95038033
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.420+2457G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95038033 | ||||||
chr8:95038058
|
A | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0158 | 12 | HG01167.hp1 HG01891.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.420+2482A>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95038058 | ||||||
chr8:95038059
|
T | A | 8 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0073others(5): Show | 8 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.420+2483T>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95038059 | ||||||
chr8:95038167
|
A | G | 12 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0062others(9): Show | 12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.420+2591A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95038167 | ||||||
chr8:95038272
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.420+2696A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95038272 | ||||||
chr8:95038311
|
G | T | 10 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0001t0004g0073others(7): Show | 10 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.420+2735G>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95038311 | ||||||
chr8:95038329
|
T | C | 88 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(85): Show | 152 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.420+2753T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95038329 | ||||||
chr8:95038654
|
T | C | 2 | a0001c0001t0001g0136a0001c0001t0001g0149 | 2 | HG02109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.421-2916T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95038654 | ||||||
chr8:95038690
|
C | T | 1 | a0001c0001t0007g0048 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.421-2880C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95038690 | ||||||
chr8:95038722
|
A | G | 190 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(187): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.421-2848A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95038722 | ||||||
chr8:95038806
|
T | C | 1 | a0001c0001t0003g0122 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.421-2764T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95038806 | ||||||
chr8:95038826
|
T | C | 4 | a0001c0001t0001g0021a0001c0001t0001g0049a0001c0001t0001g0055others(1): Show | 5 | NA18948.hp1 NA18950.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.421-2744T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95038826 | ||||||
chr8:95038905
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.421-2665G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95038905 | ||||||
chr8:95038920
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.421-2650C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95038920 | ||||||
chr8:95038959
|
G | A | 6 | a0001c0001t0001g0014a0001c0001t0001g0081a0001c0001t0001g0082others(3): Show | 8 | HG00639.hp1 HG00741.hp2 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.421-2611G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95038959 | ||||||
chr8:95038983
|
G | GT | 31 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0026others(28): Show | 36 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.421-2576dupT | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 95038983 | |||||
chr8:95038984
|
T | G | 8 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0073others(5): Show | 8 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.421-2586T>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95038984 | ||||||
chr8:95038986
|
T | C | 3 | a0001c0001t0001g0019a0001c0001t0001g0042a0001c0001t0001g0201 | 6 | HG00621.hp1 NA18747.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.421-2584T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95038986 | ||||||
chr8:95039121
|
T | C | 190 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(187): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.421-2449T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95039121 | ||||||
chr8:95039326
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.421-2244G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95039326 | ||||||
chr8:95039377
|
G | A | 1 | a0001c0001t0001g0160 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.421-2193G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95039377 | ||||||
chr8:95039462
|
A | G | 1 | a0001c0001t0001g0013 | 3 | HG02080.hp2 HG02523.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.421-2108A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95039462 | ||||||
chr8:95039463
|
A | C | 3 | a0001c0001t0002g0121a0001c0001t0002g0127a0001c0007t0002g0128 | 3 | HG01109.hp2 HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.421-2107A>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95039463 | ||||||
chr8:95039463
|
A | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 266 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.421-2107A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95039463 | ||||||
chr8:95039471
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.421-2099T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95039471 | ||||||
chr8:95039533
|
C | G | 4 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0003t0008g0052others(1): Show | 4 | HG01261.hp1 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.421-2037C>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95039533 | ||||||
chr8:95039567
|
C | T | 1 | a0001c0001t0007g0048 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.421-2003C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95039567 | ||||||
chr8:95039572
|
C | T | 5 | a0001c0001t0003g0012a0001c0001t0003g0122a0001c0001t0003g0124others(2): Show | 8 | HG02145.hp2 HG02257.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.421-1998C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95039572 | ||||||
chr8:95039627
|
T | TA | 3 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068 | 3 | HG01891.hp2 HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.421-1942dupA | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 95039627 | |||||
chr8:95039646
|
A | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(205): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.421-1924A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95039646 | ||||||
chr8:95039822
|
A | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 266 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.421-1748A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95039822 | ||||||
chr8:95039824
|
G | A | 1 | a0001c0001t0002g0129 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.421-1746G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95039824 | ||||||
chr8:95039840
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.421-1730T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95039840 | ||||||
chr8:95039924
|
C | T | 1 | a0001c0006t0004g0070 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.421-1646C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95039924 | ||||||
chr8:95040086
|
T | A | 12 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0062others(9): Show | 12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.421-1484T>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95040086 | ||||||
chr8:95040174
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.421-1396G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95040174 | ||||||
chr8:95040174
|
G | C | 12 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0062others(9): Show | 12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.421-1396G>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95040174 | ||||||
chr8:95040193
|
A | G | 1 | a0001c0001t0004g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.421-1377A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95040193 | ||||||
chr8:95040504
|
A | G | 2 | a0001c0001t0004g0046a0001c0001t0004g0047 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.421-1066A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95040504 | ||||||
chr8:95040659
|
G | GT | 5 | a0001c0001t0004g0073a0001c0001t0004g0074a0001c0002t0005g0075others(2): Show | 5 | HG02257.hp1 HG02976.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.421-905dupT | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 95040659 | |||||
chr8:95040692
|
A | C | 1 | a0001c0001t0001g0084 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.421-878A>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95040692 | ||||||
chr8:95040727
|
G | A | 9 | a0001c0001t0001g0161a0001c0001t0004g0046a0001c0001t0004g0047others(6): Show | 9 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.421-843G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95040727 | ||||||
chr8:95040861
|
G | A | 12 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0062others(9): Show | 12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.421-709G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95040861 | ||||||
chr8:95041009
|
A | T | 8 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0073others(5): Show | 8 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.421-561A>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95041009 | ||||||
chr8:95041074
|
C | T | 1 | a0001c0001t0001g0095 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.421-496C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95041074 | ||||||
chr8:95041159
|
G | A | 1 | a0001c0001t0001g0056 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.421-411G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95041159 | ||||||
chr8:95041230
|
A | T | 1 | a0001c0001t0001g0100 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.421-340A>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95041230 | ||||||
chr8:95041263
|
C | T | 12 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0062others(9): Show | 12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.421-307C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95041263 | ||||||
chr8:95041380
|
A | T | 1 | a0001c0001t0001g0157 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.421-190A>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95041380 | ||||||
chr8:95041554
|
GCT | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 266 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.421-13_421-12delCT | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 95041554 | |||||
chr8:95041772
|
C | T | 87 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(84): Show | 151 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.477+146C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95041772 | ||||||
chr8:95041790
|
C | T | 2 | a0001c0001t0001g0040a0001c0001t0001g0195 | 3 | HG03654.hp2 HG03927.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.477+164C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95041790 | ||||||
chr8:95041820
|
A | C | 12 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0062others(9): Show | 12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.477+194A>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95041820 | ||||||
chr8:95041866
|
T | G | 1 | a0001c0006t0004g0070 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.477+240T>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95041866 | ||||||
chr8:95042036
|
A | G | 3 | a0001c0001t0002g0121a0001c0001t0002g0127a0001c0007t0002g0128 | 3 | HG01109.hp2 HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.477+410A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95042036 | ||||||
chr8:95042088
|
C | T | 3 | a0001c0001t0003g0012a0001c0001t0003g0122a0001c0001t0003g0126 | 6 | HG02257.hp2 HG02622.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.477+462C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95042088 | ||||||
chr8:95042160
|
G | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0199 | 3 | NA18981.hp1 NA18999.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.477+534G>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95042160 | ||||||
chr8:95042188
|
T | C | 1 | a0001c0001t0004g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.477+562T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95042188 | ||||||
chr8:95042381
|
G | A | 5 | a0001c0001t0004g0073a0001c0001t0004g0074a0001c0002t0005g0075others(2): Show | 5 | HG02257.hp1 HG02976.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.477+755G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95042381 | ||||||
chr8:95042765
|
C | T | 12 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0062others(9): Show | 12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.477+1139C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95042765 | ||||||
chr8:95042920
|
C | A | 12 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0062others(9): Show | 12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.477+1294C>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95042920 | ||||||
chr8:95043086
|
C | CT | 17 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0021others(14): Show | 28 | HG00544.hp2 HG00735.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.477+1477dupT | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr8 | 95043086 | |||||
chr8:95043086
|
CT | C | 12 | a0001c0001t0001g0088a0001c0001t0001g0101a0001c0001t0001g0102others(9): Show | 12 | HG01168.hp1 HG01168.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.477+1477delT | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr8 | 95043086 | |||||
chr8:95043086
|
CTT | C | 7 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0073others(4): Show | 7 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.477+1476_477+1477d others(4): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr8 | 95043086 | |||||
chr8:95043153
|
C | T | 3 | a0001c0001t0001g0018a0001c0001t0001g0183a0001c0001t0001g0191 | 5 | HG00642.hp2 HG01074.hp1 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.477+1527C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95043153 | ||||||
chr8:95043170
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.477+1544C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95043170 | ||||||
chr8:95043194
|
C | A | 1 | a0001c0006t0004g0070 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.477+1568C>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95043194 | ||||||
chr8:95043194
|
C | T | 1 | a0001c0001t0001g0120 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.477+1568C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95043194 | ||||||
chr8:95043245
|
C | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0027 | 5 | HG02055.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.477+1619C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95043245 | ||||||
chr8:95043246
|
G | A | 3 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133 | 3 | HG00140.hp1 HG01496.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.477+1620G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95043246 | ||||||
chr8:95043251
|
AT | A | 12 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0062others(9): Show | 12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.477+1637delT | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr8 | 95043251 | |||||
chr8:95043306
|
G | T | 1 | a0001c0001t0001g0102 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.477+1680G>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95043306 | ||||||
chr8:95043336
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.477+1710G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95043336 | ||||||
chr8:95043373
|
G | A | 1 | a0001c0001t0001g0164 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.477+1747G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95043373 | ||||||
chr8:95043458
|
GA | G | 21 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0021others(18): Show | 29 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.477+1839delA | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr8 | 95043458 | |||||
chr8:95043476
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.477+1850G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95043476 | ||||||
chr8:95043481
|
A | G | 59 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(56): Show | 98 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.477+1855A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95043481 | ||||||
chr8:95043519
|
ACT | A | 4 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0003t0008g0052others(1): Show | 4 | HG01261.hp1 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.477+1896_477+1897d others(4): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr8 | 95043519 | |||||
chr8:95043534
|
G | C | 12 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0062others(9): Show | 12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.477+1908G>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95043534 | ||||||
chr8:95043548
|
T | C | 12 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0062others(9): Show | 12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.477+1922T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95043548 | ||||||
chr8:95043972
|
G | A | 2 | a0001c0001t0004g0046a0001c0001t0004g0047 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.478-1573G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95043972 | ||||||
chr8:95044224
|
G | T | 1 | a0001c0001t0001g0061 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.478-1321G>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95044224 | ||||||
chr8:95044225
|
G | T | 8 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0003g0012others(5): Show | 14 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.478-1320G>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95044225 | ||||||
chr8:95044388
|
A | G | 3 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0003t0008g0052 | 3 | HG02258.hp1 HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.478-1157A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95044388 | ||||||
chr8:95044451
|
C | CT | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(166): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.478-1076dupT | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr8 | 95044451 | |||||
chr8:95044451
|
C | CTT | 13 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0102others(10): Show | 22 | HG01167.hp1 HG01433.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.478-1077_478-1076d others(4): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr8 | 95044451 | |||||
chr8:95044508
|
A | G | 6 | a0001c0001t0004g0073a0001c0001t0004g0074a0001c0001t0007g0048others(3): Show | 6 | HG02257.hp1 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.478-1037A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95044508 | ||||||
chr8:95044577
|
C | G | 1 | a0001c0001t0001g0066 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.478-968C>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95044577 | ||||||
chr8:95044577
|
C | T | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(156): Show | 271 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.478-968C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95044577 | ||||||
chr8:95044685
|
A | G | 2 | a0001c0001t0001g0067a0001c0001t0001g0068 | 2 | HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.478-860A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95044685 | ||||||
chr8:95044693
|
T | C | 8 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0073others(5): Show | 8 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-852T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95044693 | ||||||
chr8:95044707
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.478-838C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95044707 | ||||||
chr8:95044745
|
C | T | 3 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0003t0008g0052 | 3 | HG02258.hp1 HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.478-800C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95044745 | ||||||
chr8:95044757
|
CT | C | 13 | a0001c0001t0001g0006a0001c0001t0001g0069a0001c0001t0001g0089others(10): Show | 19 | HG00544.hp1 HG01070.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.478-774delT | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr8 | 95044757 | |||||
chr8:95044796
|
C | T | 1 | a0001c0001t0007g0048 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.478-749C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95044796 | ||||||
chr8:95044856
|
T | C | 4 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0003t0008g0052others(1): Show | 4 | HG01261.hp1 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.478-689T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95044856 | ||||||
chr8:95044888
|
C | T | 8 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0073others(5): Show | 8 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-657C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95044888 | ||||||
chr8:95044962
|
A | G | 1 | a0001c0001t0001g0179 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.478-583A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95044962 | ||||||
chr8:95045065
|
T | TC | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 266 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.478-477dupC | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr8 | 95045065 | |||||
chr8:95045068
|
C | T | 1 | a0001c0001t0007g0048 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.478-477C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95045068 | ||||||
chr8:95045137
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.478-408A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95045137 | ||||||
chr8:95045179
|
G | A | 5 | a0001c0001t0001g0019a0001c0001t0001g0042a0001c0001t0001g0201others(2): Show | 8 | HG00621.hp1 HG02040.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.478-366G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95045179 | ||||||
chr8:95045179
|
G | T | 34 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(31): Show | 45 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.478-366G>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95045179 | ||||||
chr8:95045221
|
C | T | 7 | a0001c0001t0001g0107a0001c0001t0001g0165a0001c0001t0004g0073others(4): Show | 7 | HG01256.hp2 HG02257.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.478-324C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95045221 | ||||||
chr8:95045229
|
C | G | 1 | a0001c0003t0008g0052 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.478-316C>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95045229 | ||||||
chr8:95045253
|
G | A | 12 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0062others(9): Show | 12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.478-292G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95045253 | ||||||
chr8:95045297
|
A | T | 6 | a0001c0001t0001g0145a0001c0001t0004g0062a0001c0001t0004g0063others(3): Show | 6 | HG00642.hp1 HG01261.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.478-248A>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95045297 | ||||||
chr8:95045329
|
A | T | 1 | a0001c0001t0004g0063 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.478-216A>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95045329 | ||||||
chr8:95045722
|
T | C | 12 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0062others(9): Show | 12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.580+75T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | chr8 | 95045722 | ||||||
chr8:95045770
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.580+123G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | chr8 | 95045770 | ||||||
chr8:95045776
|
G | GTT | 12 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0062others(9): Show | 12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.580+136_580+137dup others(2): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr8 | 95045776 | |||||
chr8:95045990
|
G | A | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(186): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.580+343G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | chr8 | 95045990 | ||||||
chr8:95046022
|
A | C | 1 | a0001c0001t0001g0085 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.580+375A>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | chr8 | 95046022 | ||||||
chr8:95046032
|
A | ATTTATTT others(3): Show |
1 | a0001c0001t0001g0178 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.580+408_580+417dup others(10): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr8 | 95046032 | |||||
chr8:95046032
|
A | ATTTATTT others(9): Show |
1 | a0001c0001t0004g0073 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.580+388_580+403dup others(16): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr8 | 95046032 | |||||
chr8:95046032
|
A | ATTTATTT others(18): Show |
1 | a0001c0001t0004g0046 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.580+393_580+417dup others(25): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr8 | 95046032 | |||||
chr8:95046032
|
A | ATTTATTT others(23): Show |
1 | a0001c0001t0004g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.580+388_580+417dup others(30): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr8 | 95046032 | |||||
chr8:95046036
|
A | ATTTTATT others(9): Show |
3 | a0001c0001t0004g0062a0001c0003t0008g0052a0001c0006t0004g0070 | 3 | HG01261.hp1 HG02258.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.580+393_580+408dup others(16): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr8 | 95046036 | |||||
chr8:95046036
|
A | ATTTTATT others(9): Show |
4 | a0001c0001t0004g0074a0001c0002t0005g0075a0001c0002t0005g0076others(1): Show | 4 | HG02257.hp1 HG02976.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.580+403_580+404ins others(16): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr8 | 95046036 | |||||
chr8:95046051
|
A | T | 1 | a0001c0001t0007g0048 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.580+404A>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | chr8 | 95046051 | ||||||
chr8:95046060
|
T | A | 2 | a0001c0001t0002g0131a0001c0001t0002g0132 | 2 | HG01496.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.580+413T>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | chr8 | 95046060 | ||||||
chr8:95046061
|
A | ATTTTATT others(13): Show |
1 | a0001c0001t0007g0048 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.580+417_580+418ins others(20): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr8 | 95046061 | |||||
chr8:95046120
|
G | A | 4 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0003t0008g0052others(1): Show | 4 | HG01261.hp1 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.580+473G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | chr8 | 95046120 | ||||||
chr8:95046122
|
T | A | 4 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0003t0008g0052others(1): Show | 4 | HG01261.hp1 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.580+475T>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | chr8 | 95046122 | ||||||
chr8:95046124
|
A | G | 4 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0003t0008g0052others(1): Show | 4 | HG01261.hp1 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.580+477A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | chr8 | 95046124 | ||||||
chr8:95046125
|
A | G | 6 | a0001c0001t0001g0066a0001c0001t0004g0073a0001c0001t0004g0074others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.580+478A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | chr8 | 95046125 | ||||||
chr8:95046215
|
C | T | 2 | a0001c0001t0001g0105a0001c0001t0001g0106 | 2 | HG00735.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.580+568C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | chr8 | 95046215 | ||||||
chr8:95046324
|
C | T | 3 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0003t0008g0052 | 3 | HG02258.hp1 HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.581-670C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | chr8 | 95046324 | ||||||
chr8:95046457
|
T | C | 2 | a0001c0001t0004g0046a0001c0001t0004g0047 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.581-537T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | chr8 | 95046457 | ||||||
chr8:95046814
|
G | C | 8 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0073others(5): Show | 8 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.581-180G>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | chr8 | 95046814 | ||||||
chr8:95046882
|
A | G | 2 | a0001c0001t0001g0038a0001c0001t0001g0177 | 3 | HG02109.hp2 HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.581-112A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | chr8 | 95046882 | ||||||
chr8:95046990
|
A | T | 12 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0062others(9): Show | 12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
splice_region_variant&intron_variant | LOW | c.581-4A>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | chr8 | 95046990 | ||||||
chr8:95047420
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.714+293C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/8 | chr8 | 95047420 | ||||||
chr8:95047438
|
CTTTAT | C | 4 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0003t0008g0052others(1): Show | 4 | HG01261.hp1 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.714+323_714+327del others(5): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr8 | 95047438 | |||||
chr8:95047507
|
T | C | 1 | a0001c0001t0003g0126 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.714+380T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/8 | chr8 | 95047507 | ||||||
chr8:95047508
|
C | CT | 8 | a0001c0001t0001g0009a0001c0001t0001g0037a0001c0001t0001g0060others(5): Show | 13 | HG01109.hp1 HG01358.hp2 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.714+400dupT | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr8 | 95047508 | |||||
chr8:95047508
|
CTT | C | 12 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0062others(9): Show | 12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.714+399_714+400del others(2): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr8 | 95047508 | |||||
chr8:95047627
|
G | A | 12 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0062others(9): Show | 12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.714+500G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/8 | chr8 | 95047627 | ||||||
chr8:95047652
|
G | A | 1 | a0001c0006t0004g0070 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.714+525G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/8 | chr8 | 95047652 | ||||||
chr8:95047659
|
G | A | 3 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0003t0008g0052 | 3 | HG02258.hp1 HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.714+532G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/8 | chr8 | 95047659 | ||||||
chr8:95047685
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.714+558A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/8 | chr8 | 95047685 | ||||||
chr8:95047712
|
T | C | 2 | a0001c0001t0001g0016a0001c0001t0001g0027 | 5 | HG02055.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.714+585T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/8 | chr8 | 95047712 | ||||||
chr8:95047744
|
C | T | 2 | a0001c0001t0001g0036a0001c0001t0001g0176 | 3 | HG02145.hp1 HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.714+617C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/8 | chr8 | 95047744 | ||||||
chr8:95047805
|
G | A | 1 | a0001c0001t0001g0030 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.715-652G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/8 | chr8 | 95047805 | ||||||
chr8:95047807
|
C | G | 22 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0021others(19): Show | 30 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.715-650C>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/8 | chr8 | 95047807 | ||||||
chr8:95047989
|
G | A | 1 | a0001c0001t0001g0032 | 2 | HG02698.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.715-468G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/8 | chr8 | 95047989 | ||||||
chr8:95048046
|
T | C | 2 | a0001c0001t0001g0038a0001c0001t0001g0177 | 3 | HG02109.hp2 HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.715-411T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/8 | chr8 | 95048046 | ||||||
chr8:95048078
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.715-379C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/8 | chr8 | 95048078 | ||||||
chr8:95048143
|
A | G | 5 | a0001c0001t0004g0073a0001c0001t0004g0074a0001c0002t0005g0075others(2): Show | 5 | HG02257.hp1 HG02976.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.715-314A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/8 | chr8 | 95048143 | ||||||
chr8:95048252
|
T | C | 12 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0062others(9): Show | 12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.715-205T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/8 | chr8 | 95048252 | ||||||
chr8:95048284
|
G | A | 8 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0073others(5): Show | 8 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.715-173G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/8 | chr8 | 95048284 | ||||||
chr8:95048314
|
G | A | 1 | a0001c0001t0001g0033 | 2 | HG01943.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.715-143G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/8 | chr8 | 95048314 | ||||||
chr8:95048334
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.715-123G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/8 | chr8 | 95048334 | ||||||
chr8:95048839
|
A | C | 1 | a0001c0001t0004g0063 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.816+281A>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95048839 | ||||||
chr8:95048842
|
GTGTCTTT others(5): Show |
G | 1 | a0001c0005t0001g0141 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.816+286_816+297del others(12): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr8 | 95048842 | |||||
chr8:95048864
|
T | C | 12 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0062others(9): Show | 12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.816+306T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95048864 | ||||||
chr8:95048887
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.816+329G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95048887 | ||||||
chr8:95049030
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.816+472A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95049030 | ||||||
chr8:95049049
|
G | A | 12 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0062others(9): Show | 12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.816+491G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95049049 | ||||||
chr8:95049124
|
C | A | 1 | a0001c0001t0001g0205 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.816+566C>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95049124 | ||||||
chr8:95049148
|
C | T | 1 | a0001c0001t0002g0129 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.816+590C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95049148 | ||||||
chr8:95049149
|
G | A | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.816+591G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95049149 | ||||||
chr8:95049195
|
C | G | 8 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0073others(5): Show | 8 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.816+637C>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95049195 | ||||||
chr8:95049209
|
CTCT | C | 6 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0092others(3): Show | 6 | NA18982.hp2 NA18986.hp2 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.816+659_816+661del others(3): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr8 | 95049209 | |||||
chr8:95049239
|
C | CTT | 12 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0062others(9): Show | 12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.816+682_816+683ins others(2): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr8 | 95049239 | |||||
chr8:95049335
|
C | T | 6 | a0001c0001t0003g0012a0001c0001t0003g0122a0001c0001t0003g0123others(3): Show | 9 | HG02145.hp2 HG02257.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.816+777C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95049335 | ||||||
chr8:95049343
|
G | T | 1 | a0001c0001t0004g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.816+785G>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95049343 | ||||||
chr8:95049391
|
A | T | 12 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0062others(9): Show | 12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.816+833A>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95049391 | ||||||
chr8:95049472
|
A | G | 12 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0062others(9): Show | 12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.816+914A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95049472 | ||||||
chr8:95049551
|
T | G | 2 | a0001c0001t0001g0103a0001c0001t0001g0112 | 2 | NA19064.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.816+993T>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95049551 | ||||||
chr8:95049732
|
G | C | 8 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0001t0004g0073others(5): Show | 8 | HG02257.hp1 HG02258.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.816+1174G>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95049732 | ||||||
chr8:95049760
|
A | G | 1 | a0001c0002t0005g0076 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.816+1202A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95049760 | ||||||
chr8:95049832
|
C | T | 1 | a0001c0001t0001g0117 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.816+1274C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95049832 | ||||||
chr8:95050139
|
G | A | 1 | a0001c0001t0001g0169 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.816+1581G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95050139 | ||||||
chr8:95050306
|
G | C | 1 | a0001c0001t0001g0025 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.816+1748G>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95050306 | ||||||
chr8:95050352
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.816+1794G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95050352 | ||||||
chr8:95050373
|
A | G | 61 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(58): Show | 103 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.817-1801A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95050373 | ||||||
chr8:95050425
|
A | C | 1 | a0001c0001t0001g0175 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.817-1749A>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95050425 | ||||||
chr8:95050702
|
T | C | 33 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0021others(30): Show | 41 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.817-1472T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95050702 | ||||||
chr8:95051184
|
T | C | 8 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0073others(5): Show | 8 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.817-990T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95051184 | ||||||
chr8:95051304
|
C | T | 3 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068 | 3 | HG01891.hp2 HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.817-870C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95051304 | ||||||
chr8:95051385
|
G | C | 6 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0092others(3): Show | 6 | NA18982.hp2 NA18986.hp2 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.817-789G>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95051385 | ||||||
chr8:95051392
|
T | C | 1 | a0001c0001t0001g0178 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.817-782T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95051392 | ||||||
chr8:95051479
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.817-695A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95051479 | ||||||
chr8:95051502
|
T | C | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.817-672T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95051502 | ||||||
chr8:95051590
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.817-584C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95051590 | ||||||
chr8:95051760
|
G | A | 9 | a0001c0001t0001g0019a0001c0001t0001g0034a0001c0001t0001g0042others(6): Show | 13 | HG00621.hp1 HG02040.hp1 HG02165.hp1 others(10): Show |
intron_variant | MODIFIER | c.817-414G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95051760 | ||||||
chr8:95051772
|
A | G | 3 | a0001c0001t0002g0129a0001c0001t0002g0130a0001c0001t0006g0028 | 4 | HG01884.hp1 HG03041.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.817-402A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95051772 | ||||||
chr8:95051808
|
G | A | 12 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0062others(9): Show | 12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.817-366G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95051808 | ||||||
chr8:95051970
|
G | C | 2 | a0001c0001t0002g0129a0001c0001t0002g0130 | 2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.817-204G>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95051970 | ||||||
chr8:95052327
|
C | T | 6 | a0001c0001t0003g0012a0001c0001t0003g0122a0001c0001t0003g0123others(3): Show | 9 | HG02145.hp2 HG02257.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.873+97C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95052327 | ||||||
chr8:95052424
|
G | A | 3 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0003t0008g0052 | 3 | HG02258.hp1 HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.873+194G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95052424 | ||||||
chr8:95052514
|
G | T | 12 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0062others(9): Show | 12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.873+284G>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95052514 | ||||||
chr8:95052579
|
T | C | 3 | a0001c0001t0001g0018a0001c0001t0001g0183a0001c0001t0001g0191 | 5 | HG00642.hp2 HG01074.hp1 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.873+349T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95052579 | ||||||
chr8:95052629
|
T | C | 12 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0062others(9): Show | 12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.873+399T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95052629 | ||||||
chr8:95052876
|
A | G | 5 | a0001c0001t0004g0073a0001c0001t0004g0074a0001c0002t0005g0075others(2): Show | 5 | HG02257.hp1 HG02976.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.873+646A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95052876 | ||||||
chr8:95053058
|
A | G | 3 | a0001c0001t0002g0129a0001c0001t0002g0130a0001c0001t0006g0028 | 4 | HG01884.hp1 HG03041.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.873+828A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95053058 | ||||||
chr8:95053150
|
A | G | 12 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0062others(9): Show | 12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.873+920A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95053150 | ||||||
chr8:95053155
|
A | T | 12 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0062others(9): Show | 12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.873+925A>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95053155 | ||||||
chr8:95053275
|
G | A | 3 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0007g0048 | 3 | HG02630.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.873+1045G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95053275 | ||||||
chr8:95053380
|
T | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0100 | 3 | HG00609.hp2 HG00673.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.873+1150T>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95053380 | ||||||
chr8:95053627
|
C | CTTT | 3 | a0001c0002t0005g0075a0001c0002t0005g0076a0001c0002t0005g0077 | 3 | HG02257.hp1 HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.873+1398_873+1400d others(5): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr8 | 95053627 | |||||
chr8:95053631
|
C | T | 11 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0062others(8): Show | 11 | HG02257.hp1 HG02258.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.873+1401C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95053631 | ||||||
chr8:95053650
|
G | A | 54 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(51): Show | 104 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.873+1420G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95053650 | ||||||
chr8:95053746
|
C | T | 3 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0007g0048 | 3 | HG02630.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.873+1516C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95053746 | ||||||
chr8:95053791
|
G | A | 12 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0062others(9): Show | 12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.873+1561G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95053791 | ||||||
chr8:95053916
|
C | T | 8 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0073others(5): Show | 8 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.873+1686C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95053916 | ||||||
chr8:95053923
|
G | A | 4 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0003t0008g0052others(1): Show | 4 | HG01261.hp1 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.873+1693G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95053923 | ||||||
chr8:95053925
|
C | CT | 128 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(125): Show | 222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.873+1722dupT | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr8 | 95053925 | |||||
chr8:95053925
|
C | CTT | 38 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0019others(35): Show | 53 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.873+1721_873+1722d others(4): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr8 | 95053925 | |||||
chr8:95053952
|
T | G | 2 | a0001c0001t0004g0062a0001c0003t0008g0052 | 2 | HG02258.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.873+1722T>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95053952 | ||||||
chr8:95054093
|
T | C | 12 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0062others(9): Show | 12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.873+1863T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95054093 | ||||||
chr8:95054237
|
G | A | 1 | a0001c0006t0004g0070 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.873+2007G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95054237 | ||||||
chr8:95054269
|
TG | T | 8 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0073others(5): Show | 8 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.873+2040delG | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95054269 | ||||||
chr8:95054355
|
G | A | 3 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0007g0048 | 3 | HG02630.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.873+2125G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95054355 | ||||||
chr8:95054418
|
C | G | 1 | a0001c0001t0001g0067 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.873+2188C>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95054418 | ||||||
chr8:95054436
|
CT | C | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(176): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.873+2222delT | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr8 | 95054436 | |||||
chr8:95054630
|
T | C | 3 | a0001c0001t0002g0121a0001c0001t0002g0127a0001c0007t0002g0128 | 3 | HG01109.hp2 HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.873+2400T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95054630 | ||||||
chr8:95054654
|
C | G | 1 | a0001c0001t0001g0116 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.873+2424C>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95054654 | ||||||
chr8:95054736
|
C | G | 1 | a0001c0001t0004g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.873+2506C>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95054736 | ||||||
chr8:95054818
|
C | T | 4 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0003t0008g0052others(1): Show | 4 | HG01261.hp1 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.873+2588C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95054818 | ||||||
chr8:95054846
|
A | C | 12 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0062others(9): Show | 12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.873+2616A>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95054846 | ||||||
chr8:95054908
|
A | T | 8 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0073others(5): Show | 8 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.873+2678A>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95054908 | ||||||
chr8:95055174
|
G | T | 1 | a0001c0001t0001g0199 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.874-2635G>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95055174 | ||||||
chr8:95055185
|
A | G | 4 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0003t0008g0052others(1): Show | 4 | HG01261.hp1 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.874-2624A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95055185 | ||||||
chr8:95055530
|
A | G | 2 | a0001c0001t0004g0046a0001c0001t0004g0047 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.874-2279A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95055530 | ||||||
chr8:95055621
|
C | T | 1 | a0001c0001t0001g0035 | 2 | HG00438.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.874-2188C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95055621 | ||||||
chr8:95055639
|
A | G | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0006g0028 | 4 | HG02723.hp1 HG02970.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.874-2170A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95055639 | ||||||
chr8:95055646
|
G | A | 1 | a0001c0001t0001g0174 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.874-2163G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95055646 | ||||||
chr8:95055660
|
G | A | 12 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0062others(9): Show | 12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.874-2149G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95055660 | ||||||
chr8:95055709
|
A | G | 5 | a0001c0001t0004g0073a0001c0001t0004g0074a0001c0002t0005g0075others(2): Show | 5 | HG02257.hp1 HG02976.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.874-2100A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95055709 | ||||||
chr8:95055830
|
A | G | 1 | a0001c0006t0004g0070 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.874-1979A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95055830 | ||||||
chr8:95056136
|
T | C | 12 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0062others(9): Show | 12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.874-1673T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95056136 | ||||||
chr8:95056152
|
C | A | 12 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0062others(9): Show | 12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.874-1657C>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95056152 | ||||||
chr8:95056195
|
C | T | 1 | a0001c0001t0007g0048 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.874-1614C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95056195 | ||||||
chr8:95056232
|
G | GT | 5 | a0001c0001t0001g0043a0001c0001t0001g0066a0001c0001t0001g0067others(2): Show | 6 | HG01891.hp2 HG02723.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.874-1564dupT | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr8 | 95056232 | |||||
chr8:95056237
|
T | A | 8 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0073others(5): Show | 8 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.874-1572T>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95056237 | ||||||
chr8:95056316
|
T | A | 1 | a0001c0001t0007g0048 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.874-1493T>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95056316 | ||||||
chr8:95056356
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.874-1453G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95056356 | ||||||
chr8:95056389
|
T | C | 4 | a0001c0001t0001g0041a0001c0001t0001g0161a0001c0001t0001g0198others(1): Show | 5 | NA18971.hp2 NA18981.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.874-1420T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95056389 | ||||||
chr8:95056605
|
G | C | 1 | a0001c0001t0004g0063 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.874-1204G>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95056605 | ||||||
chr8:95056632
|
T | C | 12 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0062others(9): Show | 12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.874-1177T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95056632 | ||||||
chr8:95056709
|
A | G | 2 | a0001c0001t0004g0046a0001c0001t0004g0047 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.874-1100A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95056709 | ||||||
chr8:95056743
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.874-1066A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95056743 | ||||||
chr8:95056837
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.874-972C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95056837 | ||||||
chr8:95056847
|
A | G | 3 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0003t0008g0052 | 3 | HG02258.hp1 HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.874-962A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95056847 | ||||||
chr8:95056855
|
G | A | 3 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0007g0048 | 3 | HG02630.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.874-954G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95056855 | ||||||
chr8:95056892
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.874-917C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95056892 | ||||||
chr8:95056905
|
C | CA | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(188): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.874-890dupA | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr8 | 95056905 | |||||
chr8:95056984
|
G | C | 1 | a0001c0001t0001g0180 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.874-825G>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95056984 | ||||||
chr8:95057073
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.874-736C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95057073 | ||||||
chr8:95057085
|
G | A | 2 | a0001c0001t0001g0067a0001c0001t0001g0068 | 2 | HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.874-724G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95057085 | ||||||
chr8:95057121
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.874-688C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95057121 | ||||||
chr8:95057122
|
G | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0177 | 3 | HG02109.hp2 HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.874-687G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95057122 | ||||||
chr8:95057268
|
G | A | 2 | a0001c0001t0004g0046a0001c0001t0004g0047 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.874-541G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95057268 | ||||||
chr8:95057326
|
T | G | 2 | a0001c0001t0004g0046a0001c0001t0004g0047 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.874-483T>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95057326 | ||||||
chr8:95057342
|
A | G | 1 | a0001c0001t0001g0173 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.874-467A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95057342 | ||||||
chr8:95057406
|
A | C | 1 | a0001c0001t0001g0173 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.874-403A>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95057406 | ||||||
chr8:95057449
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.874-360G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95057449 | ||||||
chr8:95057573
|
T | G | 1 | a0001c0001t0001g0201 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.874-236T>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95057573 | ||||||
chr8:95057601
|
A | G | 8 | a0001c0001t0004g0046a0001c0001t0004g0047a0001c0001t0004g0073others(5): Show | 8 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.874-208A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95057601 | ||||||
chr8:95057651
|
CTTT | C | 3 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0003t0008g0052 | 3 | HG02258.hp1 HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.874-155_874-153del others(3): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr8 | 95057651 | |||||
chr8:95057699
|
C | G | 1 | a0001c0001t0001g0090 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.874-110C>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95057699 | ||||||
chr8:95057739
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.874-70T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95057739 | ||||||
chr8:95057745
|
G | GT | 19 | a0001c0001t0001g0026a0001c0001t0001g0078a0001c0001t0001g0113others(16): Show | 20 | HG00438.hp1 HG02155.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.874-50dupT | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr8 | 95057745 |