Item | Value |
---|---|
geneid | 55967 |
ensemblid | ENSG00000184752.14 |
hgncid | 23987 |
symbol | NDUFA12 |
name | NADH:ubiquinone oxidoreductase subunit A12 |
refseq_nuc | NM_018838.5 |
refseq_prot | NP_061326.1 |
ensembl_nuc | ENST00000327772.7 |
ensembl_prot | ENSP00000330737.2 |
mane_status | MANE Select |
chr | chr12 |
start | 94971333 |
end | 95003697 |
strand | - |
ver | v1.2 |
region | chr12:94971333-95003697 |
region5000 | chr12:94966333-95008697 |
regionname0 | NDUFA12_chr12_94971333_95003697 |
regionname5000 | NDUFA12_chr12_94966333_95008697 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 435 | 439 | 90 | 78 | 205 | 18 | 46 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | ATGGA others(430): Show |
chr12 | 94966333 | 95008697 | ||
a0001c0002 | 0/0 | 435 | 3 | 0 | 0 | 3 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | ATGGA others(430): Show |
chr12 | 94966333 | 95008697 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 562 | 437 | 89 | 78 | 204 | 18 | 46 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | GGGGC others(557): Show |
chr12 | 94966333 | 95008697 |
a0001c0001t0002 | 0/0 | 562 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | GGGGC others(557): Show |
chr12 | 94966333 | 95008697 |
a0001c0001t0003 | 0/0 | 562 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | GGGGC others(557): Show |
chr12 | 94966333 | 95008697 |
a0001c0002t0001 | 0/0 | 562 | 3 | 0 | 0 | 3 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | GGGGC others(557): Show |
chr12 | 94966333 | 95008697 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 1/0 | 14 | 0 | 4 | 8 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0002 | 0/0 | 12 | 0 | 2 | 9 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0003 | 0/0 | 9 | 1 | 2 | 5 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0004 | 0/0 | 8 | 0 | 3 | 5 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0005 | 0/0 | 7 | 4 | 1 | 0 | 0 | 2 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0006 | 0/0 | 7 | 0 | 2 | 4 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0007 | 0/0 | 7 | 0 | 1 | 5 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0008 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0009 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0010 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0014 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0021 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0046 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0054 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0162 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0001t0003g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0089 | EUR | GBR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0025 | EUR | GBR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0101 | EUR | GBR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0088 | EUR | GBR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0257 | EUR | FIN | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0112 | EUR | FIN | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0103 | EUR | FIN | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | CHS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | CHS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | CHS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | IBS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0050 | EUR | IBS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0133 | EUR | IBS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0050 | EUR | IBS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0168 | EUR | IBS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | PEL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | KHV | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CDX | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CDX | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | CDX | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CDX | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ESN | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | ESN | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | MSL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | ESN | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ESN | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | ESN | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | MSL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | MSL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | MSL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | MSL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | MSL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ESN | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0298 | SAS | STU | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | STU | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | BEB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | BEB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | BEB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | BEB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | BEB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | BEB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | STU | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | BEB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | STU | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0299 | SAS | STU | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | STU | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | STU | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | STU | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0312 | AFR | YRI | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | YRI | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CHB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | LWK | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | LWK | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | LWK | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | LWK | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19055 | hp1 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19070 | hp2 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19077 | hp2 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | YRI | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ASW | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ASW | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | TSI | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0294 | EUR | TSI | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0056 | EUR | TSI | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | TSI | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | GIH | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | GIH | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | USA | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | USA | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | USA | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | USA | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | LWK | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | LWK | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0162 | REF | REF | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
view | 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 |
---|
view | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:94994211 | G | A | 1 | a0001c0002 | 3 | NA19055.hp1 NA19070.hp2 NA19077.hp2 |
synonymous_variant | LOW | c.216C>T | p.Asn72Asn | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/4 | 233/562 | 216/438 | 72/145 | chr12 | 94994211 |
view | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:94971378 | G | A | 1 | a0001c0001t0002 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*62C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 4/4 | 62 | chr12 | 94971378 | ||||||
chr12:95003691 | T | G | 1 | a0001c0001t0003 | 1 | NA18522.hp1 | 5_prime_UTR_variant | MODIFIER | c.-11A>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 1/4 | 11 | chr12 | 95003691 |
view | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:94971974 | A | G | 6 | a0001c0001t0001g0027 a0001c0001t0001g0078 a0001c0001t0001g0090 others(3): Show |
7 | HG02055.hp2 HG02145.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.258-354T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94971974 | |||||||
chr12:94972023 | T | C | 75 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0010 others(72): Show |
103 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.258-403A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94972023 | |||||||
chr12:94972060 | C | T | 78 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0010 others(75): Show |
106 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.258-440G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94972060 | |||||||
chr12:94972362 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.258-742G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94972362 | |||||||
chr12:94972374 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.258-754A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94972374 | |||||||
chr12:94972532 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.258-912C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94972532 | |||||||
chr12:94972549 | T | A | 1 | a0001c0001t0001g0173 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.258-929A>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94972549 | |||||||
chr12:94972630 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.258-1010C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94972630 | |||||||
chr12:94972633 | G | T | 1 | a0001c0001t0001g0236 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.258-1013C>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94972633 | |||||||
chr12:94972736 | T | C | 1 | a0001c0001t0001g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.258-1116A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94972736 | |||||||
chr12:94972782 | A | C | 34 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(31): Show |
63 | HG00438.hp1 HG00438.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.258-1162T>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94972782 | |||||||
chr12:94972829 | T | C | 34 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(31): Show |
63 | HG00438.hp1 HG00438.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.258-1209A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94972829 | |||||||
chr12:94972879 | T | TGCGATCA others(1): Show |
165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.258-1260_258-1259i others(10): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94972879 | |||||||
chr12:94973244 | G | C | 1 | a0001c0001t0001g0117 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.258-1624C>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94973244 | |||||||
chr12:94973803 | C | G | 4 | a0001c0001t0001g0293 a0001c0001t0001g0295 a0001c0001t0001g0296 others(1): Show |
4 | HG02965.hp2 HG03540.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.258-2183G>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94973803 | |||||||
chr12:94973872 | C | A | 114 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(111): Show |
150 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.258-2252G>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94973872 | |||||||
chr12:94973946 | C | T | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(119): Show |
158 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.258-2326G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94973946 | |||||||
chr12:94973968 | C | CT | 11 | a0001c0001t0001g0046 a0001c0001t0001g0093 a0001c0001t0001g0125 others(8): Show |
12 | HG01433.hp1 HG01978.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.258-2349dupA | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94973968 | |||||||
chr12:94973968 | C | CTT | 30 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(27): Show |
59 | HG00438.hp1 HG00438.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.258-2350_258-2349d others(4): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94973968 | |||||||
chr12:94973968 | C | CTTT | 7 | a0001c0001t0001g0040 a0001c0001t0001g0136 a0001c0001t0001g0143 others(4): Show |
8 | HG03540.hp1 NA18961.hp1 NA18968.hp2 others(5): Show |
intron_variant | MODIFIER | c.258-2351_258-2349d others(5): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94973968 | |||||||
chr12:94973968 | CT | C | 101 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(98): Show |
135 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.258-2349delA | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94973968 | |||||||
chr12:94974011 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.258-2391C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94974011 | |||||||
chr12:94974127 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.258-2507T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94974127 | |||||||
chr12:94974132 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.258-2512C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94974132 | |||||||
chr12:94974375 | G | A | 9 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0056 others(6): Show |
11 | HG00099.hp2 HG00642.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.258-2755C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94974375 | |||||||
chr12:94974387 | A | G | 34 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(31): Show |
63 | HG00438.hp1 HG00438.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.258-2767T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94974387 | |||||||
chr12:94974401 | G | A | 112 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(109): Show |
148 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.258-2781C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94974401 | |||||||
chr12:94974463 | C | A | 75 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0010 others(72): Show |
103 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.258-2843G>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94974463 | |||||||
chr12:94974618 | G | A | 94 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(91): Show |
126 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.258-2998C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94974618 | |||||||
chr12:94974722 | G | A | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.258-3102C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94974722 | |||||||
chr12:94974914 | TAGTC | T | 3 | a0001c0001t0001g0023 a0001c0001t0001g0061 a0001c0001t0001g0062 |
4 | HG00642.hp2 HG00733.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-3298_258-3295d others(6): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94974914 | |||||||
chr12:94974927 | T | A | 1 | a0001c0001t0001g0255 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.258-3307A>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94974927 | |||||||
chr12:94974946 | G | C | 1 | a0001c0001t0001g0141 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.258-3326C>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94974946 | |||||||
chr12:94974953 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.258-3333G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94974953 | |||||||
chr12:94974988 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.258-3368A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94974988 | |||||||
chr12:94975205 | A | G | 1 | a0001c0001t0001g0029 | 2 | HG02258.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.258-3585T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94975205 | |||||||
chr12:94975240 | T | C | 1 | a0001c0001t0001g0307 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.258-3620A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94975240 | |||||||
chr12:94975394 | A | G | 3 | a0001c0001t0001g0053 a0001c0001t0001g0260 a0001c0001t0001g0268 |
4 | HG02257.hp2 HG02647.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.258-3774T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94975394 | |||||||
chr12:94975589 | T | C | 1 | a0001c0001t0001g0258 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.258-3969A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94975589 | |||||||
chr12:94975639 | T | A | 26 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0026 others(23): Show |
40 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.258-4019A>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94975639 | |||||||
chr12:94975754 | T | C | 1 | a0001c0001t0001g0227 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.258-4134A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94975754 | |||||||
chr12:94975828 | C | G | 1 | a0001c0001t0001g0069 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.258-4208G>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94975828 | |||||||
chr12:94975828 | C | T | 2 | a0001c0001t0001g0283 a0001c0001t0001g0285 |
2 | NA18995.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.258-4208G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94975828 | |||||||
chr12:94975947 | G | A | 32 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(29): Show |
61 | HG00438.hp1 HG00438.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.258-4327C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94975947 | |||||||
chr12:94976012 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.258-4392C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94976012 | |||||||
chr12:94976037 | G | A | 1 | a0001c0001t0001g0255 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.258-4417C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94976037 | |||||||
chr12:94976038 | A | AAG | 6 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0215 others(3): Show |
6 | HG00558.hp1 HG00673.hp1 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.258-4420_258-4419d others(4): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94976038 | |||||||
chr12:94976038 | A | G | 1 | a0001c0001t0001g0255 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.258-4418T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94976038 | |||||||
chr12:94976140 | G | A | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
200 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.258-4520C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94976140 | |||||||
chr12:94976227 | T | A | 1 | a0001c0001t0001g0199 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.258-4607A>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94976227 | |||||||
chr12:94976250 | C | T | 75 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0010 others(72): Show |
103 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.258-4630G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94976250 | |||||||
chr12:94976334 | A | C | 9 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0056 others(6): Show |
11 | HG00099.hp2 HG00642.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.258-4714T>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94976334 | |||||||
chr12:94976340 | A | G | 9 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0056 others(6): Show |
11 | HG00099.hp2 HG00642.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.258-4720T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94976340 | |||||||
chr12:94976384 | G | A | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.258-4764C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94976384 | |||||||
chr12:94976462 | C | T | 33 | a0001c0001t0001g0021 a0001c0001t0001g0052 a0001c0001t0001g0074 others(30): Show |
36 | HG00423.hp2 HG00738.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.258-4842G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94976462 | |||||||
chr12:94976669 | T | C | 26 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0026 others(23): Show |
40 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.258-5049A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94976669 | |||||||
chr12:94976701 | G | A | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.258-5081C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94976701 | |||||||
chr12:94976716 | T | C | 1 | a0001c0001t0001g0270 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.258-5096A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94976716 | |||||||
chr12:94976739 | G | A | 75 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0010 others(72): Show |
103 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.258-5119C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94976739 | |||||||
chr12:94976847 | T | C | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.258-5227A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94976847 | |||||||
chr12:94977063 | G | T | 4 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0001g0081 others(1): Show |
6 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.258-5443C>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94977063 | |||||||
chr12:94977067 | G | A | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.258-5447C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94977067 | |||||||
chr12:94977409 | T | C | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.258-5789A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94977409 | |||||||
chr12:94977428 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.258-5808G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94977428 | |||||||
chr12:94977467 | T | A | 1 | a0001c0001t0001g0306 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.258-5847A>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94977467 | |||||||
chr12:94977470 | CA | C | 262 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(259): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.258-5851delT | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94977470 | |||||||
chr12:94977482 | A | C | 26 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0026 others(23): Show |
40 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.258-5862T>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94977482 | |||||||
chr12:94977503 | A | C | 104 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(101): Show |
146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.258-5883T>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94977503 | |||||||
chr12:94977513 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.258-5893G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94977513 | |||||||
chr12:94977558 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.258-5938G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94977558 | |||||||
chr12:94977622 | G | C | 33 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(30): Show |
62 | HG00438.hp1 HG00438.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.258-6002C>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94977622 | |||||||
chr12:94977638 | C | T | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.258-6018G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94977638 | |||||||
chr12:94977686 | A | G | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.258-6066T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94977686 | |||||||
chr12:94977761 | T | A | 1 | a0001c0001t0001g0255 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.258-6141A>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94977761 | |||||||
chr12:94977883 | T | C | 2 | a0001c0001t0001g0215 a0001c0001t0001g0311 |
2 | NA18956.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.258-6263A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94977883 | |||||||
chr12:94977949 | G | C | 2 | a0001c0001t0001g0215 a0001c0001t0001g0311 |
2 | NA18956.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.258-6329C>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94977949 | |||||||
chr12:94978028 | GTT | G | 25 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(22): Show |
29 | HG00099.hp2 HG00597.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.258-6410_258-6409d others(4): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94978028 | |||||||
chr12:94978052 | A | G | 1 | a0001c0001t0001g0309 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.258-6432T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94978052 | |||||||
chr12:94978255 | G | A | 2 | a0001c0001t0001g0226 a0001c0001t0001g0307 |
2 | HG01884.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.258-6635C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94978255 | |||||||
chr12:94978522 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.258-6902A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94978522 | |||||||
chr12:94978539 | G | A | 3 | a0001c0001t0001g0283 a0001c0001t0001g0285 a0001c0001t0001g0286 |
3 | NA18940.hp2 NA18995.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.258-6919C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94978539 | |||||||
chr12:94978600 | G | C | 1 | a0001c0001t0001g0199 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.258-6980C>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94978600 | |||||||
chr12:94978957 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.258-7337T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94978957 | |||||||
chr12:94979053 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.258-7433T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94979053 | |||||||
chr12:94979163 | G | A | 279 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(276): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.258-7543C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94979163 | |||||||
chr12:94979194 | T | C | 5 | a0001c0001t0001g0138 a0001c0001t0001g0194 a0001c0001t0001g0201 others(2): Show |
5 | HG02280.hp1 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.258-7574A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94979194 | |||||||
chr12:94979230 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.258-7610G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94979230 | |||||||
chr12:94979319 | T | C | 279 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(276): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.258-7699A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94979319 | |||||||
chr12:94979518 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.258-7898C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94979518 | |||||||
chr12:94979557 | GAGGTGGC others(6247): Show |
G | 1 | a0001c0002t0001g0058 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.257+8359_258-7938d others(2): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94979557 | |||||||
chr12:94979667 | T | TA | 26 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(23): Show |
30 | HG00099.hp2 HG00597.hp2 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.258-8048dupT | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94979667 | |||||||
chr12:94979667 | TA | T | 78 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0010 others(75): Show |
106 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.258-8048delT | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94979667 | |||||||
chr12:94979693 | G | T | 10 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0174 others(7): Show |
15 | HG00408.hp2 HG00597.hp1 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.258-8073C>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94979693 | |||||||
chr12:94979721 | G | A | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.258-8101C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94979721 | |||||||
chr12:94979835 | C | CA | 134 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(131): Show |
178 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.258-8216dupT | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94979835 | |||||||
chr12:94979835 | C | CAA | 5 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0255 others(2): Show |
8 | HG01891.hp2 HG02280.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.258-8217_258-8216d others(4): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94979835 | |||||||
chr12:94979999 | G | A | 26 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0026 others(23): Show |
40 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.258-8379C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94979999 | |||||||
chr12:94980071 | C | G | 1 | a0001c0001t0001g0220 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.258-8451G>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94980071 | |||||||
chr12:94980163 | C | T | 6 | a0001c0001t0001g0055 a0001c0001t0001g0134 a0001c0001t0001g0135 others(3): Show |
7 | HG02559.hp1 HG02630.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.258-8543G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94980163 | |||||||
chr12:94980293 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.258-8673G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94980293 | |||||||
chr12:94980313 | C | A | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.258-8693G>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94980313 | |||||||
chr12:94980450 | C | T | 1 | a0001c0001t0001g0227 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.258-8830G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94980450 | |||||||
chr12:94980484 | C | T | 34 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(31): Show |
63 | HG00438.hp1 HG00438.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.258-8864G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94980484 | |||||||
chr12:94980487 | T | C | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.258-8867A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94980487 | |||||||
chr12:94980534 | T | C | 1 | a0001c0001t0001g0005 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.258-8914A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94980534 | |||||||
chr12:94980586 | TA | T | 286 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(283): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.258-8967delT | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94980586 | |||||||
chr12:94980662 | A | C | 2 | a0001c0001t0001g0226 a0001c0001t0001g0307 |
2 | HG01884.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.258-9042T>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94980662 | |||||||
chr12:94980673 | A | C | 25 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(22): Show |
29 | HG00099.hp2 HG00597.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.258-9053T>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94980673 | |||||||
chr12:94980739 | T | C | 34 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(31): Show |
63 | HG00438.hp1 HG00438.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.258-9119A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94980739 | |||||||
chr12:94980745 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.258-9125C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94980745 | |||||||
chr12:94980768 | C | T | 111 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(108): Show |
147 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.258-9148G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94980768 | |||||||
chr12:94980816 | G | GT | 36 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(33): Show |
65 | HG00438.hp1 HG00438.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.258-9197dupA | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94980816 | |||||||
chr12:94980854 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.258-9234G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94980854 | |||||||
chr12:94980865 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.258-9245T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94980865 | |||||||
chr12:94981205 | G | A | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.258-9585C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94981205 | |||||||
chr12:94981269 | A | AATAC | 153 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(150): Show |
218 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.258-9653_258-9650d others(6): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94981269 | |||||||
chr12:94981269 | A | AATACATA others(1): Show |
120 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(117): Show |
165 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.258-9657_258-9650d others(10): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94981269 | |||||||
chr12:94981293 | C | CATAT | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0183 |
3 | HG02717.hp2 HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.258-9674_258-9673i others(6): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94981293 | |||||||
chr12:94981319 | G | A | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.258-9699C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94981319 | |||||||
chr12:94981341 | C | T | 34 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(31): Show |
63 | HG00438.hp1 HG00438.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.258-9721G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94981341 | |||||||
chr12:94981342 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.258-9722C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94981342 | |||||||
chr12:94981380 | C | T | 25 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(22): Show |
29 | HG00099.hp2 HG00597.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.258-9760G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94981380 | |||||||
chr12:94981392 | A | G | 1 | a0001c0001t0001g0245 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.258-9772T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94981392 | |||||||
chr12:94981392 | A | T | 1 | a0001c0001t0001g0199 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.258-9772T>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94981392 | |||||||
chr12:94981404 | C | T | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.258-9784G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94981404 | |||||||
chr12:94981429 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.258-9809A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94981429 | |||||||
chr12:94981630 | G | A | 10 | a0001c0001t0001g0108 a0001c0001t0001g0138 a0001c0001t0001g0194 others(7): Show |
10 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.258-10010C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94981630 | |||||||
chr12:94981664 | G | A | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.258-10044C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94981664 | |||||||
chr12:94981692 | A | G | 26 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0026 others(23): Show |
40 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.258-10072T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94981692 | |||||||
chr12:94981753 | T | C | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.258-10133A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94981753 | |||||||
chr12:94981754 | G | A | 1 | a0001c0001t0001g0003 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.258-10134C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94981754 | |||||||
chr12:94981875 | G | T | 1 | a0001c0001t0001g0005 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.258-10255C>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94981875 | |||||||
chr12:94981914 | A | C | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.258-10294T>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94981914 | |||||||
chr12:94981942 | G | A | 25 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(22): Show |
29 | HG00099.hp2 HG00597.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.258-10322C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94981942 | |||||||
chr12:94981985 | T | C | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.258-10365A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94981985 | |||||||
chr12:94981997 | A | G | 78 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0010 others(75): Show |
106 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.258-10377T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94981997 | |||||||
chr12:94982046 | G | A | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.258-10426C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94982046 | |||||||
chr12:94982134 | T | C | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.258-10514A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94982134 | |||||||
chr12:94982259 | A | G | 4 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0206 others(1): Show |
4 | NA18954.hp2 NA19010.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.258-10639T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94982259 | |||||||
chr12:94982275 | CTTTT | C | 275 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(272): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.258-10659_258-1065 others(8): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94982275 | |||||||
chr12:94982280 | T | C | 5 | a0001c0001t0001g0108 a0001c0001t0001g0195 a0001c0001t0001g0196 others(2): Show |
5 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.258-10660A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94982280 | |||||||
chr12:94982409 | G | C | 3 | a0001c0001t0001g0013 a0001c0001t0001g0305 a0001c0001t0001g0306 |
6 | HG01891.hp2 HG02280.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.258-10789C>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94982409 | |||||||
chr12:94982466 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.258-10846G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94982466 | |||||||
chr12:94982502 | A | T | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.258-10882T>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94982502 | |||||||
chr12:94982563 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.258-10943G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94982563 | |||||||
chr12:94982594 | G | A | 1 | a0001c0001t0001g0005 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.258-10974C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94982594 | |||||||
chr12:94982636 | A | G | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.258-11016T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94982636 | |||||||
chr12:94982688 | C | T | 131 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(128): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.258-11068G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94982688 | |||||||
chr12:94982696 | G | A | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.258-11076C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94982696 | |||||||
chr12:94982731 | C | T | 25 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(22): Show |
29 | HG00099.hp2 HG00597.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.258-11111G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94982731 | |||||||
chr12:94983037 | T | G | 1 | a0001c0001t0001g0034 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.257+11133A>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94983037 | |||||||
chr12:94983384 | T | G | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.257+10786A>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94983384 | |||||||
chr12:94983428 | T | C | 288 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(285): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.257+10742A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94983428 | |||||||
chr12:94983519 | C | T | 111 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(108): Show |
147 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.257+10651G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94983519 | |||||||
chr12:94983521 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.257+10649G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94983521 | |||||||
chr12:94983559 | T | C | 6 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0129 others(3): Show |
8 | HG00733.hp1 HG01192.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.257+10611A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94983559 | |||||||
chr12:94983592 | G | A | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.257+10578C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94983592 | |||||||
chr12:94983714 | T | C | 131 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(128): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.257+10456A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94983714 | |||||||
chr12:94983736 | C | T | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.257+10434G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94983736 | |||||||
chr12:94983767 | GCTT | G | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.257+10400_257+1040 others(7): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94983767 | |||||||
chr12:94983800 | C | A | 1 | a0001c0001t0001g0227 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.257+10370G>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94983800 | |||||||
chr12:94983825 | C | G | 1 | a0001c0001t0001g0141 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.257+10345G>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94983825 | |||||||
chr12:94983885 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.257+10285G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94983885 | |||||||
chr12:94983895 | A | AGACATCT | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.257+10274_257+1027 others(11): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94983895 | |||||||
chr12:94983916 | G | A | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.257+10254C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94983916 | |||||||
chr12:94983917 | G | A | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.257+10253C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94983917 | |||||||
chr12:94984162 | T | C | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(144): Show |
212 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(209): Show |
intron_variant | MODIFIER | c.257+10008A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94984162 | |||||||
chr12:94984434 | G | A | 2 | a0001c0001t0001g0075 a0001c0001t0001g0076 |
2 | HG00597.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.257+9736C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94984434 | |||||||
chr12:94984460 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.257+9710G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94984460 | |||||||
chr12:94984487 | G | A | 5 | a0001c0001t0001g0138 a0001c0001t0001g0194 a0001c0001t0001g0201 others(2): Show |
5 | HG02280.hp1 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.257+9683C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94984487 | |||||||
chr12:94984488 | C | T | 5 | a0001c0001t0001g0138 a0001c0001t0001g0194 a0001c0001t0001g0201 others(2): Show |
5 | HG02280.hp1 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.257+9682G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94984488 | |||||||
chr12:94984507 | G | T | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(144): Show |
212 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(209): Show |
intron_variant | MODIFIER | c.257+9663C>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94984507 | |||||||
chr12:94984546 | G | A | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.257+9624C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94984546 | |||||||
chr12:94984550 | C | CA | 6 | a0001c0001t0001g0049 a0001c0001t0001g0138 a0001c0001t0001g0194 others(3): Show |
6 | HG00544.hp2 HG02280.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.257+9619dupT | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94984550 | |||||||
chr12:94984611 | G | C | 1 | a0001c0001t0001g0192 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.257+9559C>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94984611 | |||||||
chr12:94984678 | A | C | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.257+9492T>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94984678 | |||||||
chr12:94984688 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.257+9482T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94984688 | |||||||
chr12:94984697 | C | T | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.257+9473G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94984697 | |||||||
chr12:94984727 | C | A | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.257+9443G>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94984727 | |||||||
chr12:94984730 | C | A | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.257+9440G>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94984730 | |||||||
chr12:94984736 | A | AAAAAC | 18 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0093 others(15): Show |
19 | HG00280.hp1 HG00423.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.257+9433_257+9434i others(7): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94984736 | |||||||
chr12:94984736 | A | AAAAC | 73 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0013 others(70): Show |
79 | HG00544.hp2 HG00609.hp2 HG01081.hp1 others(76): Show |
intron_variant | MODIFIER | c.257+9433_257+9434i others(6): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94984736 | |||||||
chr12:94984736 | A | AAAC | 167 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(164): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.257+9433_257+9434i others(5): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94984736 | |||||||
chr12:94984736 | A | AAC | 33 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(30): Show |
58 | HG00438.hp2 HG00735.hp1 HG01074.hp1 others(55): Show |
intron_variant | MODIFIER | c.257+9433_257+9434i others(4): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94984736 | |||||||
chr12:94984736 | A | AC | 4 | a0001c0001t0001g0009 a0001c0001t0001g0149 a0001c0001t0001g0150 others(1): Show |
4 | HG01168.hp2 NA18982.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.257+9433dupG | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94984736 | |||||||
chr12:94984736 | A | C | 1 | a0001c0001t0001g0006 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.257+9434T>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94984736 | |||||||
chr12:94984750 | A | T | 1 | a0001c0001t0001g0185 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.257+9420T>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94984750 | |||||||
chr12:94984803 | C | A | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.257+9367G>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94984803 | |||||||
chr12:94984807 | A | G | 1 | a0001c0001t0001g0226 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.257+9363T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94984807 | |||||||
chr12:94984892 | T | C | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.257+9278A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94984892 | |||||||
chr12:94984931 | TCGCACCA others(1): Show |
T | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.257+9231_257+9238d others(10): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94984931 | |||||||
chr12:94984997 | C | CATAACAT others(8): Show |
145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(142): Show |
210 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(207): Show |
intron_variant | MODIFIER | c.257+9172_257+9173i others(17): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94984997 | |||||||
chr12:94985002 | C | CATAACAT others(3): Show |
1 | a0001c0001t0001g0226 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.257+9167_257+9168i others(12): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94985002 | |||||||
chr12:94985002 | C | CATAACAT others(13): Show |
77 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0010 others(74): Show |
105 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.257+9167_257+9168i others(22): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94985002 | |||||||
chr12:94985002 | C | CATAACAT others(18): Show |
23 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0026 others(20): Show |
35 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.257+9167_257+9168i others(27): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94985002 | |||||||
chr12:94985002 | C | CATAACAT others(23): Show |
6 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0001g0081 others(3): Show |
8 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.257+9167_257+9168i others(32): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94985002 | |||||||
chr12:94985002 | C | CATAACAT others(28): Show |
21 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(18): Show |
25 | HG00099.hp2 HG00597.hp2 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.257+9167_257+9168i others(37): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94985002 | |||||||
chr12:94985002 | C | CATAACAT others(33): Show |
3 | a0001c0001t0001g0063 a0001c0001t0001g0071 a0001c0001t0001g0073 |
3 | HG03491.hp1 HG03492.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.257+9167_257+9168i others(42): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94985002 | |||||||
chr12:94985002 | C | CATAACAT others(38): Show |
1 | a0001c0001t0001g0134 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.257+9167_257+9168i others(47): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94985002 | |||||||
chr12:94985007 | A | C | 1 | a0001c0001t0001g0226 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.257+9163T>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94985007 | |||||||
chr12:94985007 | A | G | 145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(142): Show |
210 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(207): Show |
intron_variant | MODIFIER | c.257+9163T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94985007 | |||||||
chr12:94985012 | G | A | 276 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(273): Show |
387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.257+9158C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94985012 | |||||||
chr12:94985042 | G | C | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.257+9128C>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94985042 | |||||||
chr12:94985043 | C | T | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0183 |
3 | HG02717.hp2 HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.257+9127G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94985043 | |||||||
chr12:94985058 | C | T | 1 | a0001c0001t0001g0009 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.257+9112G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94985058 | |||||||
chr12:94985071 | C | T | 1 | a0001c0001t0001g0029 | 2 | HG02258.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.257+9099G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94985071 | |||||||
chr12:94985168 | T | A | 2 | a0001c0001t0001g0083 a0001c0001t0001g0087 |
2 | HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.257+9002A>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94985168 | |||||||
chr12:94985172 | T | A | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.257+8998A>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94985172 | |||||||
chr12:94985220 | G | A | 1 | a0001c0001t0001g0310 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.257+8950C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94985220 | |||||||
chr12:94985221 | A | T | 1 | a0001c0001t0001g0200 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.257+8949T>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94985221 | |||||||
chr12:94985312 | G | A | 279 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(276): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.257+8858C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94985312 | |||||||
chr12:94985362 | C | T | 34 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(31): Show |
63 | HG00438.hp1 HG00438.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.257+8808G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94985362 | |||||||
chr12:94985379 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.257+8791G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94985379 | |||||||
chr12:94985380 | G | A | 12 | a0001c0001t0001g0015 a0001c0001t0001g0032 a0001c0001t0001g0104 others(9): Show |
15 | HG02165.hp1 NA18944.hp1 NA18950.hp2 others(12): Show |
intron_variant | MODIFIER | c.257+8790C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94985380 | |||||||
chr12:94985491 | GTGGTCAG others(52): Show |
G | 1 | a0001c0001t0001g0307 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.257+8620_257+8678d others(61): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94985491 | |||||||
chr12:94985500 | G | A | 1 | a0001c0001t0001g0272 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.257+8670C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94985500 | |||||||
chr12:94985528 | G | C | 10 | a0001c0001t0001g0108 a0001c0001t0001g0138 a0001c0001t0001g0194 others(7): Show |
10 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.257+8642C>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94985528 | |||||||
chr12:94985575 | T | C | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.257+8595A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94985575 | |||||||
chr12:94985626 | C | CA | 47 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(44): Show |
53 | HG00099.hp2 HG00423.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.257+8543dupT | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94985626 | |||||||
chr12:94985626 | C | CAA | 69 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0010 others(66): Show |
91 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.257+8542_257+8543d others(4): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94985626 | |||||||
chr12:94985626 | C | CAAA | 21 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0035 others(18): Show |
22 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(19): Show |
intron_variant | MODIFIER | c.257+8541_257+8543d others(5): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94985626 | |||||||
chr12:94985664 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.257+8506T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94985664 | |||||||
chr12:94985715 | A | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0118 others(3): Show |
6 | HG01433.hp1 HG02004.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.257+8455T>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94985715 | |||||||
chr12:94985777 | G | C | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(307): Show |
436 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(433): Show |
intron_variant | MODIFIER | c.257+8393C>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94985777 | |||||||
chr12:94985795 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0062 |
2 | HG01261.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.257+8375A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94985795 | |||||||
chr12:94985813 | A | G | 1 | a0001c0002t0001g0058 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.257+8357T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94985813 | |||||||
chr12:94985913 | C | A | 1 | a0001c0001t0001g0085 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.257+8257G>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94985913 | |||||||
chr12:94985914 | G | A | 6 | a0001c0001t0001g0055 a0001c0001t0001g0134 a0001c0001t0001g0135 others(3): Show |
7 | HG02559.hp1 HG02630.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.257+8256C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94985914 | |||||||
chr12:94985948 | G | A | 279 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(276): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.257+8222C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94985948 | |||||||
chr12:94985982 | G | C | 1 | a0001c0001t0001g0148 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.257+8188C>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94985982 | |||||||
chr12:94986000 | G | A | 25 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(22): Show |
29 | HG00099.hp2 HG00597.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.257+8170C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94986000 | |||||||
chr12:94986026 | G | A | 289 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(286): Show |
400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
intron_variant | MODIFIER | c.257+8144C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94986026 | |||||||
chr12:94986030 | A | G | 26 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0026 others(23): Show |
40 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.257+8140T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94986030 | |||||||
chr12:94986041 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.257+8129G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94986041 | |||||||
chr12:94986063 | C | T | 245 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(242): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.257+8107G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94986063 | |||||||
chr12:94986085 | C | CTAAA | 113 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0010 others(110): Show |
144 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.257+8081_257+8084d others(6): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94986085 | |||||||
chr12:94986085 | C | CTAAATAA others(1): Show |
40 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0016 others(37): Show |
57 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.257+8077_257+8084d others(10): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94986085 | |||||||
chr12:94986085 | C | CTAAATAA others(5): Show |
2 | a0001c0001t0001g0194 a0001c0001t0001g0203 |
2 | HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.257+8073_257+8084d others(14): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94986085 | |||||||
chr12:94986085 | CTAAA | C | 36 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(33): Show |
65 | HG00438.hp1 HG00438.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.257+8081_257+8084d others(6): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94986085 | |||||||
chr12:94986115 | A | T | 34 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(31): Show |
63 | HG00438.hp1 HG00438.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.257+8055T>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94986115 | |||||||
chr12:94986230 | G | C | 131 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(128): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.257+7940C>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94986230 | |||||||
chr12:94986288 | C | T | 2 | a0001c0001t0001g0226 a0001c0001t0001g0307 |
2 | HG01884.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.257+7882G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94986288 | |||||||
chr12:94986403 | A | G | 1 | a0001c0001t0001g0164 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.257+7767T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94986403 | |||||||
chr12:94986456 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.257+7714G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94986456 | |||||||
chr12:94986494 | C | T | 245 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(242): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.257+7676G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94986494 | |||||||
chr12:94986531 | T | C | 245 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(242): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.257+7639A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94986531 | |||||||
chr12:94986564 | T | C | 78 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0010 others(75): Show |
106 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.257+7606A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94986564 | |||||||
chr12:94986642 | AC | A | 244 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(241): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.257+7527delG | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94986642 | |||||||
chr12:94986643 | C | A | 1 | a0001c0001t0001g0255 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.257+7527G>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94986643 | |||||||
chr12:94986644 | C | A | 26 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0026 others(23): Show |
40 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.257+7526G>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94986644 | |||||||
chr12:94986669 | G | A | 6 | a0001c0001t0001g0055 a0001c0001t0001g0134 a0001c0001t0001g0135 others(3): Show |
7 | HG02559.hp1 HG02630.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.257+7501C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94986669 | |||||||
chr12:94986678 | G | C | 25 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(22): Show |
29 | HG00099.hp2 HG00597.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.257+7492C>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94986678 | |||||||
chr12:94986820 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.257+7350G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94986820 | |||||||
chr12:94986876 | AG | A | 78 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0010 others(75): Show |
106 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.257+7293delC | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94986876 | |||||||
chr12:94987002 | C | T | 1 | a0001c0001t0001g0241 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.257+7168G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94987002 | |||||||
chr12:94987312 | A | G | 34 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(31): Show |
63 | HG00438.hp1 HG00438.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.257+6858T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94987312 | |||||||
chr12:94987495 | A | G | 1 | a0001c0001t0001g0216 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.257+6675T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94987495 | |||||||
chr12:94987519 | G | A | 34 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(31): Show |
63 | HG00438.hp1 HG00438.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.257+6651C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94987519 | |||||||
chr12:94987627 | C | T | 1 | a0001c0001t0001g0199 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.257+6543G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94987627 | |||||||
chr12:94987733 | C | T | 4 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0129 others(1): Show |
6 | HG00733.hp1 HG01192.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.257+6437G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94987733 | |||||||
chr12:94987745 | C | G | 10 | a0001c0001t0001g0108 a0001c0001t0001g0138 a0001c0001t0001g0194 others(7): Show |
10 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.257+6425G>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94987745 | |||||||
chr12:94987776 | G | A | 245 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(242): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.257+6394C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94987776 | |||||||
chr12:94987785 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.257+6385A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94987785 | |||||||
chr12:94987791 | C | CA | 7 | a0001c0001t0001g0138 a0001c0001t0001g0203 a0001c0001t0001g0214 others(4): Show |
7 | HG02074.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.257+6378dupT | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94987791 | |||||||
chr12:94987791 | CA | C | 172 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(169): Show |
236 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.257+6378delT | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94987791 | |||||||
chr12:94987791 | CAA | C | 37 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0026 others(34): Show |
50 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.257+6377_257+6378d others(4): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94987791 | |||||||
chr12:94987791 | CAAA | C | 27 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(24): Show |
31 | HG00099.hp2 HG00597.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.257+6376_257+6378d others(5): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94987791 | |||||||
chr12:94987791 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0143 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.257+6367_257+6378d others(14): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94987791 | |||||||
chr12:94987791 | CAAAAAAA others(6): Show |
C | 33 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(30): Show |
62 | HG00438.hp1 HG00438.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.257+6366_257+6378d others(15): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94987791 | |||||||
chr12:94987818 | G | T | 10 | a0001c0001t0001g0108 a0001c0001t0001g0138 a0001c0001t0001g0194 others(7): Show |
10 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.257+6352C>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94987818 | |||||||
chr12:94987839 | A | T | 2 | a0001c0001t0001g0071 a0001c0001t0001g0073 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.257+6331T>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94987839 | |||||||
chr12:94987870 | C | T | 112 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(109): Show |
148 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.257+6300G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94987870 | |||||||
chr12:94987926 | A | G | 245 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(242): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.257+6244T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94987926 | |||||||
chr12:94988009 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.257+6161G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94988009 | |||||||
chr12:94988226 | C | T | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0183 |
3 | HG02717.hp2 HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.257+5944G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94988226 | |||||||
chr12:94988318 | A | G | 1 | a0001c0001t0001g0149 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.257+5852T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94988318 | |||||||
chr12:94988339 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.257+5831G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94988339 | |||||||
chr12:94988347 | CTAAAG | C | 4 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0271 others(1): Show |
4 | HG02027.hp1 NA18978.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.257+5818_257+5822d others(7): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94988347 | |||||||
chr12:94988362 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.257+5808C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94988362 | |||||||
chr12:94988424 | C | A | 1 | a0001c0001t0001g0049 | 2 | HG00544.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.257+5746G>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94988424 | |||||||
chr12:94988424 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.257+5746G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94988424 | |||||||
chr12:94988620 | C | T | 112 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(109): Show |
148 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.257+5550G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94988620 | |||||||
chr12:94988661 | G | A | 34 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(31): Show |
63 | HG00438.hp1 HG00438.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.257+5509C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94988661 | |||||||
chr12:94988711 | T | C | 279 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(276): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.257+5459A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94988711 | |||||||
chr12:94988763 | C | G | 8 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0204 others(5): Show |
14 | HG00609.hp1 HG02132.hp1 NA18944.hp2 others(11): Show |
intron_variant | MODIFIER | c.257+5407G>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94988763 | |||||||
chr12:94988809 | C | G | 131 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(128): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.257+5361G>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94988809 | |||||||
chr12:94988825 | C | T | 114 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(111): Show |
150 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.257+5345G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94988825 | |||||||
chr12:94988862 | T | C | 34 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(31): Show |
63 | HG00438.hp1 HG00438.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.257+5308A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94988862 | |||||||
chr12:94989120 | T | C | 34 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(31): Show |
63 | HG00438.hp1 HG00438.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.257+5050A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94989120 | |||||||
chr12:94989362 | A | C | 1 | a0001c0001t0001g0101 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.257+4808T>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94989362 | |||||||
chr12:94989395 | A | G | 34 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(31): Show |
63 | HG00438.hp1 HG00438.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.257+4775T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94989395 | |||||||
chr12:94989630 | C | T | 3 | a0001c0001t0001g0194 a0001c0001t0001g0201 a0001c0001t0001g0203 |
3 | HG02622.hp1 HG02647.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.257+4540G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94989630 | |||||||
chr12:94989674 | T | C | 112 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(109): Show |
148 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.257+4496A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94989674 | |||||||
chr12:94989687 | G | A | 1 | a0001c0001t0001g0050 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.257+4483C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94989687 | |||||||
chr12:94989779 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.257+4391C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94989779 | |||||||
chr12:94989846 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.257+4324G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94989846 | |||||||
chr12:94989939 | T | C | 279 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(276): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.257+4231A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94989939 | |||||||
chr12:94990261 | A | G | 94 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(91): Show |
126 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.257+3909T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94990261 | |||||||
chr12:94990271 | G | GA | 115 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(112): Show |
151 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.257+3898dupT | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94990271 | |||||||
chr12:94990271 | GA | G | 110 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(107): Show |
167 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.257+3898delT | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94990271 | |||||||
chr12:94990272 | A | G | 26 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0026 others(23): Show |
40 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.257+3898T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94990272 | |||||||
chr12:94990278 | A | AC | 25 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(22): Show |
29 | HG00099.hp2 HG00597.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.257+3891_257+3892i others(3): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94990278 | |||||||
chr12:94990291 | A | C | 2 | a0001c0001t0001g0265 a0001c0001t0001g0272 |
2 | NA19011.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.257+3879T>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94990291 | |||||||
chr12:94990427 | G | A | 34 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(31): Show |
63 | HG00438.hp1 HG00438.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.257+3743C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94990427 | |||||||
chr12:94990456 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.257+3714A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94990456 | |||||||
chr12:94990588 | A | G | 2 | a0001c0001t0001g0298 a0001c0001t0001g0299 |
2 | HG03688.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.257+3582T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94990588 | |||||||
chr12:94990626 | T | C | 78 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0010 others(75): Show |
106 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.257+3544A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94990626 | |||||||
chr12:94990718 | A | C | 1 | a0001c0001t0001g0119 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.257+3452T>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94990718 | |||||||
chr12:94990855 | A | C | 1 | a0001c0001t0001g0098 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.257+3315T>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94990855 | |||||||
chr12:94990912 | A | G | 289 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(286): Show |
400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
intron_variant | MODIFIER | c.257+3258T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94990912 | |||||||
chr12:94990999 | A | G | 5 | a0001c0001t0001g0108 a0001c0001t0001g0195 a0001c0001t0001g0196 others(2): Show |
5 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.257+3171T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94990999 | |||||||
chr12:94991370 | G | C | 4 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0272 others(1): Show |
4 | NA18975.hp2 NA18977.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.257+2800C>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94991370 | |||||||
chr12:94991430 | G | GA | 34 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(31): Show |
63 | HG00438.hp1 HG00438.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.257+2739dupT | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94991430 | |||||||
chr12:94991470 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.257+2700C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94991470 | |||||||
chr12:94991481 | A | ACTTTGCG others(4): Show |
1 | a0001c0001t0001g0119 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.257+2678_257+2688d others(13): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94991481 | |||||||
chr12:94991627 | T | C | 148 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(145): Show |
213 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(210): Show |
intron_variant | MODIFIER | c.257+2543A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94991627 | |||||||
chr12:94991726 | C | CA | 10 | a0001c0001t0001g0108 a0001c0001t0001g0128 a0001c0001t0001g0132 others(7): Show |
10 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.257+2443dupT | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94991726 | |||||||
chr12:94991726 | C | CAA | 34 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(31): Show |
63 | HG00438.hp1 HG00438.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.257+2442_257+2443d others(4): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94991726 | |||||||
chr12:94991726 | C | CAAA | 113 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(110): Show |
149 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.257+2441_257+2443d others(5): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94991726 | |||||||
chr12:94991860 | T | G | 10 | a0001c0001t0001g0108 a0001c0001t0001g0138 a0001c0001t0001g0194 others(7): Show |
10 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.257+2310A>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94991860 | |||||||
chr12:94991879 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.257+2291C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94991879 | |||||||
chr12:94992093 | T | G | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0183 |
3 | HG02717.hp2 HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.257+2077A>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94992093 | |||||||
chr12:94992102 | T | C | 2 | a0001c0001t0001g0243 a0001c0001t0001g0248 |
2 | HG01993.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.257+2068A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94992102 | |||||||
chr12:94992195 | A | G | 148 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(145): Show |
213 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(210): Show |
intron_variant | MODIFIER | c.257+1975T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94992195 | |||||||
chr12:94992504 | T | C | 18 | a0001c0001t0001g0013 a0001c0001t0001g0054 a0001c0001t0001g0107 others(15): Show |
22 | HG00741.hp1 HG01168.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.257+1666A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94992504 | |||||||
chr12:94992546 | T | G | 1 | a0001c0001t0001g0253 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.257+1624A>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94992546 | |||||||
chr12:94992548 | T | G | 3 | a0001c0001t0001g0023 a0001c0001t0001g0061 a0001c0001t0001g0062 |
4 | HG00642.hp2 HG00733.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.257+1622A>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94992548 | |||||||
chr12:94992585 | T | C | 1 | a0001c0001t0001g0226 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.257+1585A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94992585 | |||||||
chr12:94992678 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.257+1492C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94992678 | |||||||
chr12:94992858 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.257+1312G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94992858 | |||||||
chr12:94992934 | T | C | 25 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(22): Show |
29 | HG00099.hp2 HG00597.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.257+1236A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94992934 | |||||||
chr12:94992945 | G | A | 114 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(111): Show |
150 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.257+1225C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94992945 | |||||||
chr12:94992988 | G | C | 1 | a0001c0001t0001g0240 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.257+1182C>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94992988 | |||||||
chr12:94993015 | G | A | 112 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(109): Show |
148 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.257+1155C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94993015 | |||||||
chr12:94993043 | A | G | 1 | a0001c0001t0001g0028 | 2 | HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.257+1127T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94993043 | |||||||
chr12:94993231 | ATAATCCC others(129): Show |
A | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(143): Show |
211 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(208): Show |
intron_variant | MODIFIER | c.257+803_257+938del | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94993231 | |||||||
chr12:94993354 | G | C | 5 | a0001c0001t0001g0108 a0001c0001t0001g0195 a0001c0001t0001g0196 others(2): Show |
5 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.257+816C>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94993354 | |||||||
chr12:94993379 | C | CT | 10 | a0001c0001t0001g0108 a0001c0001t0001g0138 a0001c0001t0001g0194 others(7): Show |
10 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.257+790dupA | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94993379 | |||||||
chr12:94993451 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.257+719G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94993451 | |||||||
chr12:94993518 | G | A | 2 | a0001c0001t0001g0075 a0001c0001t0001g0076 |
2 | HG00597.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.257+652C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94993518 | |||||||
chr12:94993587 | T | C | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(143): Show |
211 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(208): Show |
intron_variant | MODIFIER | c.257+583A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94993587 | |||||||
chr12:94993624 | C | CA | 24 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0044 others(21): Show |
31 | HG00140.hp2 HG00621.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.257+545dupT | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94993624 | |||||||
chr12:94993624 | C | CAA | 10 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(7): Show |
13 | HG00099.hp2 HG00609.hp2 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.257+544_257+545dup others(2): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94993624 | |||||||
chr12:94993624 | C | CAAA | 9 | a0001c0001t0001g0057 a0001c0001t0001g0061 a0001c0001t0001g0062 others(6): Show |
9 | HG00642.hp2 HG01106.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.257+543_257+545dup others(3): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94993624 | |||||||
chr12:94993624 | C | CAAAAAA | 22 | a0001c0001t0001g0019 a0001c0001t0001g0051 a0001c0001t0001g0052 others(19): Show |
26 | HG00558.hp2 HG01123.hp2 HG01993.hp1 others(23): Show |
intron_variant | MODIFIER | c.257+540_257+545dup others(6): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94993624 | |||||||
chr12:94993624 | C | CAAAAAAA | 34 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0020 others(31): Show |
51 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.257+539_257+545dup others(7): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94993624 | |||||||
chr12:94993624 | C | CAAAAAAA others(1): Show |
26 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0049 others(23): Show |
36 | HG00544.hp2 HG00609.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.257+538_257+545dup others(8): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94993624 | |||||||
chr12:94993624 | C | CAAAAAAA others(3): Show |
2 | a0001c0001t0001g0276 a0001c0001t0001g0282 |
2 | HG00423.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.257+536_257+545dup others(10): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94993624 | |||||||
chr12:94993624 | C | CAAAAAAA others(6): Show |
8 | a0001c0001t0001g0133 a0001c0001t0001g0168 a0001c0001t0001g0229 others(5): Show |
8 | HG01168.hp1 HG01169.hp2 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.257+533_257+545dup others(13): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94993624 | |||||||
chr12:94993624 | C | CAAAAAAA others(7): Show |
3 | a0001c0001t0001g0054 a0001c0001t0001g0295 a0001c0001t0001g0297 |
4 | HG03540.hp2 HG03831.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.257+532_257+545dup others(14): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94993624 | |||||||
chr12:94993624 | C | CAAAAAAA others(8): Show |
2 | a0001c0001t0001g0231 a0001c0001t0001g0299 |
2 | HG00741.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.257+531_257+545dup others(15): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94993624 | |||||||
chr12:94993624 | C | CAAAAAAA others(16): Show |
1 | a0001c0001t0001g0306 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.257+523_257+545dup others(23): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94993624 | |||||||
chr12:94993624 | CA | C | 82 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(79): Show |
130 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.257+545delT | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94993624 | |||||||
chr12:94993624 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0118 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.257+536_257+545del others(10): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94993624 | |||||||
chr12:94993732 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.257+438G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94993732 | |||||||
chr12:94993733 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.257+437C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94993733 | |||||||
chr12:94993751 | A | C | 1 | a0001c0001t0001g0141 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.257+419T>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94993751 | |||||||
chr12:94993760 | A | C | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(143): Show |
211 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(208): Show |
intron_variant | MODIFIER | c.257+410T>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94993760 | |||||||
chr12:94993766 | C | T | 133 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(130): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.257+404G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94993766 | |||||||
chr12:94993780 | C | T | 106 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(103): Show |
148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.257+390G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94993780 | |||||||
chr12:94993913 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.257+257C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94993913 | |||||||
chr12:94993980 | C | T | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(143): Show |
211 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(208): Show |
intron_variant | MODIFIER | c.257+190G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94993980 | |||||||
chr12:94994008 | C | T | 28 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0043 others(25): Show |
41 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.257+162G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94994008 | |||||||
chr12:94994408 | C | T | 25 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0026 others(22): Show |
39 | HG00140.hp2 HG00639.hp1 HG01169.hp1 others(36): Show |
intron_variant | MODIFIER | c.170-151G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94994408 | |||||||
chr12:94994834 | G | T | 1 | a0001c0001t0001g0114 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.170-577C>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94994834 | |||||||
chr12:94994953 | T | C | 4 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0075 others(1): Show |
4 | HG00597.hp2 HG00673.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.170-696A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94994953 | |||||||
chr12:94995051 | A | G | 6 | a0001c0001t0001g0027 a0001c0001t0001g0078 a0001c0001t0001g0090 others(3): Show |
7 | HG02055.hp2 HG02145.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.170-794T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94995051 | |||||||
chr12:94995067 | T | C | 92 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(89): Show |
124 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.170-810A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94995067 | |||||||
chr12:94995257 | G | A | 3 | a0001c0001t0001g0194 a0001c0001t0001g0201 a0001c0001t0001g0203 |
3 | HG02622.hp1 HG02647.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.170-1000C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94995257 | |||||||
chr12:94995268 | A | G | 25 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0017 others(22): Show |
50 | HG00438.hp1 HG00438.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.170-1011T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94995268 | |||||||
chr12:94995278 | C | T | 2 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
2 | HG01256.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.170-1021G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94995278 | |||||||
chr12:94995331 | C | A | 1 | a0001c0001t0001g0226 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.170-1074G>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94995331 | |||||||
chr12:94995361 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.170-1104C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94995361 | |||||||
chr12:94995457 | G | C | 25 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(22): Show |
29 | HG00099.hp2 HG00597.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.170-1200C>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94995457 | |||||||
chr12:94995506 | A | G | 2 | a0001c0001t0001g0158 a0001c0001t0001g0186 |
2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.170-1249T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94995506 | |||||||
chr12:94995507 | C | A | 2 | a0001c0001t0001g0158 a0001c0001t0001g0186 |
2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.170-1250G>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94995507 | |||||||
chr12:94995568 | C | T | 9 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0056 others(6): Show |
11 | HG00099.hp2 HG00642.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.170-1311G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94995568 | |||||||
chr12:94995669 | GAC | G | 110 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(107): Show |
146 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.170-1414_170-1413d others(4): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94995669 | |||||||
chr12:94995849 | T | C | 10 | a0001c0001t0001g0108 a0001c0001t0001g0138 a0001c0001t0001g0194 others(7): Show |
10 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.170-1592A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94995849 | |||||||
chr12:94995901 | A | AT | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(126): Show |
190 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(187): Show |
intron_variant | MODIFIER | c.170-1645dupA | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94995901 | |||||||
chr12:94995901 | A | ATT | 18 | a0001c0001t0001g0013 a0001c0001t0001g0054 a0001c0001t0001g0107 others(15): Show |
22 | HG00741.hp1 HG01168.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.170-1646_170-1645d others(4): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94995901 | |||||||
chr12:94995924 | A | G | 1 | a0001c0001t0001g0224 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.170-1667T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94995924 | |||||||
chr12:94995972 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.170-1715G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94995972 | |||||||
chr12:94996025 | T | C | 16 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0060 others(13): Show |
27 | HG00408.hp2 HG00597.hp1 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.170-1768A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94996025 | |||||||
chr12:94996133 | G | A | 5 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0285 others(2): Show |
5 | NA18940.hp2 NA18966.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.170-1876C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94996133 | |||||||
chr12:94996237 | A | G | 133 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(130): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.170-1980T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94996237 | |||||||
chr12:94996324 | T | TAC | 40 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(37): Show |
61 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.170-2069_170-2068d others(4): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94996324 | |||||||
chr12:94996324 | T | TACAC | 8 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0197 others(5): Show |
11 | HG00280.hp1 HG01515.hp2 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.170-2071_170-2068d others(6): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94996324 | |||||||
chr12:94996324 | T | TACACAC | 9 | a0001c0001t0001g0020 a0001c0001t0001g0051 a0001c0001t0001g0108 others(6): Show |
12 | HG02055.hp1 HG02132.hp2 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.170-2073_170-2068d others(8): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94996324 | |||||||
chr12:94996324 | T | TACACACA others(1): Show |
25 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0052 others(22): Show |
31 | HG00423.hp2 HG00639.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.170-2075_170-2068d others(10): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94996324 | |||||||
chr12:94996324 | T | TACACACA others(3): Show |
18 | a0001c0001t0001g0013 a0001c0001t0001g0138 a0001c0001t0001g0201 others(15): Show |
21 | HG01361.hp1 HG01891.hp2 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.170-2077_170-2068d others(12): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94996324 | |||||||
chr12:94996324 | T | TACACACA others(5): Show |
11 | a0001c0001t0001g0054 a0001c0001t0001g0107 a0001c0001t0001g0194 others(8): Show |
12 | HG00741.hp1 HG01168.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.170-2079_170-2068d others(14): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94996324 | |||||||
chr12:94996324 | T | TACACACA others(7): Show |
2 | a0001c0001t0001g0287 a0001c0001t0003g0312 |
2 | HG03942.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.170-2081_170-2068d others(16): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94996324 | |||||||
chr12:94996324 | T | TACACACA others(9): Show |
3 | a0001c0001t0001g0196 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG01884.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.170-2083_170-2068d others(18): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94996324 | |||||||
chr12:94996324 | T | TATACAC | 3 | a0001c0001t0001g0143 a0001c0001t0001g0148 a0001c0001t0001g0199 |
3 | HG02523.hp1 NA18968.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.170-2068_170-2067i others(8): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94996324 | |||||||
chr12:94996324 | T | TATACACA others(1): Show |
28 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(25): Show |
56 | HG00438.hp1 HG00438.hp2 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.170-2068_170-2067i others(10): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94996324 | |||||||
chr12:94996324 | T | TATACACA others(3): Show |
2 | a0001c0001t0001g0041 a0001c0001t0001g0159 |
3 | HG03490.hp2 NA18953.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.170-2068_170-2067i others(12): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94996324 | |||||||
chr12:94996324 | T | TATACACA others(7): Show |
1 | a0001c0001t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.170-2068_170-2067i others(16): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94996324 | |||||||
chr12:94996324 | TACAC | T | 6 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(3): Show |
6 | HG00621.hp1 HG02027.hp1 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.170-2071_170-2068d others(6): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94996324 | |||||||
chr12:94996324 | TACACAC | T | 74 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0010 others(71): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.170-2073_170-2068d others(8): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94996324 | |||||||
chr12:94996324 | TACACACA others(1): Show |
T | 30 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(27): Show |
34 | HG00099.hp2 HG00597.hp2 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.170-2075_170-2068d others(10): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94996324 | |||||||
chr12:94996324 | TACACACA others(3): Show |
T | 25 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0026 others(22): Show |
39 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.170-2077_170-2068d others(12): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94996324 | |||||||
chr12:94996326 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.170-2069G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94996326 | |||||||
chr12:94996328 | C | T | 1 | a0001c0001t0001g0307 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.170-2071G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94996328 | |||||||
chr12:94996358 | C | CACACACA others(5): Show |
2 | a0001c0001t0001g0133 a0001c0001t0001g0168 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.170-2102_170-2101i others(14): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94996358 | |||||||
chr12:94996368 | GTC | G | 34 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(31): Show |
63 | HG00438.hp1 HG00438.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.170-2113_170-2112d others(4): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94996368 | |||||||
chr12:94996380 | C | T | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG00280.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.170-2123G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94996380 | |||||||
chr12:94996387 | T | C | 1 | a0001c0001t0001g0055 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.170-2130A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94996387 | |||||||
chr12:94996402 | G | A | 2 | a0001c0001t0001g0226 a0001c0001t0001g0307 |
2 | HG01884.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.170-2145C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94996402 | |||||||
chr12:94996591 | G | A | 2 | a0001c0001t0001g0226 a0001c0001t0001g0307 |
2 | HG01884.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.170-2334C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94996591 | |||||||
chr12:94996602 | G | A | 112 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(109): Show |
148 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.170-2345C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94996602 | |||||||
chr12:94996667 | A | C | 8 | a0001c0001t0001g0035 a0001c0001t0001g0103 a0001c0001t0001g0112 others(5): Show |
9 | HG00280.hp2 HG00323.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.170-2410T>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94996667 | |||||||
chr12:94996763 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.170-2506C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94996763 | |||||||
chr12:94996819 | C | CA | 30 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0026 others(27): Show |
44 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.170-2563dupT | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94996819 | |||||||
chr12:94996819 | C | CAA | 114 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0010 others(111): Show |
146 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.170-2564_170-2563d others(4): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94996819 | |||||||
chr12:94996819 | CA | C | 55 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(52): Show |
88 | HG00438.hp1 HG00438.hp2 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.170-2563delT | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94996819 | |||||||
chr12:94996865 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.170-2608C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94996865 | |||||||
chr12:94996955 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.170-2698G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94996955 | |||||||
chr12:94997034 | G | T | 77 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0010 others(74): Show |
105 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.170-2777C>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94997034 | |||||||
chr12:94997119 | T | C | 5 | a0001c0001t0001g0108 a0001c0001t0001g0195 a0001c0001t0001g0196 others(2): Show |
5 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.170-2862A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94997119 | |||||||
chr12:94997164 | G | T | 133 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(130): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.170-2907C>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94997164 | |||||||
chr12:94997166 | C | T | 34 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(31): Show |
63 | HG00438.hp1 HG00438.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.170-2909G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94997166 | |||||||
chr12:94997187 | ACACACAC others(3): Show |
A | 24 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(21): Show |
28 | HG00099.hp2 HG00597.hp2 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.170-2940_170-2931d others(12): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94997187 | |||||||
chr12:94997188 | C | A | 1 | a0001c0001t0001g0141 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.170-2931G>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94997188 | |||||||
chr12:94997192 | C | T | 26 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0026 others(23): Show |
40 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.170-2935G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94997192 | |||||||
chr12:94997195 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.170-2938T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94997195 | |||||||
chr12:94997197 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.170-2940C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94997197 | |||||||
chr12:94997214 | CAT | C | 34 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(31): Show |
63 | HG00438.hp1 HG00438.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.170-2959_170-2958d others(4): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94997214 | |||||||
chr12:94997236 | C | T | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(143): Show |
211 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(208): Show |
intron_variant | MODIFIER | c.170-2979G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94997236 | |||||||
chr12:94997321 | G | A | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(143): Show |
211 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(208): Show |
intron_variant | MODIFIER | c.170-3064C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94997321 | |||||||
chr12:94997609 | C | T | 34 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(31): Show |
63 | HG00438.hp1 HG00438.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.170-3352G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94997609 | |||||||
chr12:94997676 | C | T | 34 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(31): Show |
63 | HG00438.hp1 HG00438.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.170-3419G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94997676 | |||||||
chr12:94997804 | T | TCAAA | 110 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(107): Show |
146 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.170-3551_170-3548d others(6): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94997804 | |||||||
chr12:94997824 | C | T | 279 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(276): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.170-3567G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94997824 | |||||||
chr12:94997857 | T | G | 3 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0292 |
3 | NA18957.hp2 NA18977.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.170-3600A>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94997857 | |||||||
chr12:94997907 | C | T | 92 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(89): Show |
124 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.170-3650G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94997907 | |||||||
chr12:94997924 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.170-3667C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94997924 | |||||||
chr12:94998100 | A | G | 148 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(145): Show |
213 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(210): Show |
intron_variant | MODIFIER | c.170-3843T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94998100 | |||||||
chr12:94998116 | CA | C | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(143): Show |
211 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(208): Show |
intron_variant | MODIFIER | c.170-3860delT | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94998116 | |||||||
chr12:94998149 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.170-3892A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94998149 | |||||||
chr12:94998378 | C | T | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(143): Show |
211 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(208): Show |
intron_variant | MODIFIER | c.170-4121G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94998378 | |||||||
chr12:94998446 | C | T | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | NA18979.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.170-4189G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94998446 | |||||||
chr12:94998725 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.169+4014A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94998725 | |||||||
chr12:94998875 | A | G | 148 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(145): Show |
213 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(210): Show |
intron_variant | MODIFIER | c.169+3864T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94998875 | |||||||
chr12:94998882 | C | G | 35 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(32): Show |
48 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.169+3857G>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94998882 | |||||||
chr12:94998884 | A | G | 94 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(91): Show |
126 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.169+3855T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94998884 | |||||||
chr12:94999060 | T | A | 289 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(286): Show |
400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
intron_variant | MODIFIER | c.169+3679A>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94999060 | |||||||
chr12:94999313 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.169+3426A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94999313 | |||||||
chr12:94999512 | A | G | 4 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0001g0231 others(1): Show |
4 | HG00741.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.169+3227T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94999512 | |||||||
chr12:94999550 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.169+3189C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94999550 | |||||||
chr12:94999620 | C | T | 133 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(130): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.169+3119G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94999620 | |||||||
chr12:94999728 | T | C | 6 | a0001c0001t0001g0055 a0001c0001t0001g0134 a0001c0001t0001g0135 others(3): Show |
7 | HG02559.hp1 HG02630.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.169+3011A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94999728 | |||||||
chr12:94999769 | A | C | 1 | a0001c0001t0001g0108 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.169+2970T>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94999769 | |||||||
chr12:94999969 | T | C | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(143): Show |
211 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(208): Show |
intron_variant | MODIFIER | c.169+2770A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94999969 | |||||||
chr12:94999994 | G | T | 1 | a0001c0001t0001g0145 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.169+2745C>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94999994 | |||||||
chr12:95000043 | C | G | 1 | a0001c0001t0003g0312 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.169+2696G>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95000043 | |||||||
chr12:95000157 | G | A | 24 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(21): Show |
28 | HG00099.hp2 HG00597.hp2 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.169+2582C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95000157 | |||||||
chr12:95000193 | G | A | 1 | a0001c0001t0001g0300 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.169+2546C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95000193 | |||||||
chr12:95000195 | G | A | 1 | a0001c0001t0001g0300 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.169+2544C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95000195 | |||||||
chr12:95000196 | G | A | 1 | a0001c0001t0001g0300 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.169+2543C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95000196 | |||||||
chr12:95000197 | C | A | 1 | a0001c0001t0001g0300 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.169+2542G>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95000197 | |||||||
chr12:95000198 | C | A | 1 | a0001c0001t0001g0300 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.169+2541G>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95000198 | |||||||
chr12:95000199 | A | G | 113 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(110): Show |
149 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.169+2540T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95000199 | |||||||
chr12:95000200 | T | A | 1 | a0001c0001t0001g0300 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.169+2539A>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95000200 | |||||||
chr12:95000201 | T | A | 1 | a0001c0001t0001g0300 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.169+2538A>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95000201 | |||||||
chr12:95000203 | T | A | 1 | a0001c0001t0001g0300 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.169+2536A>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95000203 | |||||||
chr12:95000204 | T | A | 1 | a0001c0001t0001g0300 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.169+2535A>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95000204 | |||||||
chr12:95000205 | C | A | 1 | a0001c0001t0001g0300 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.169+2534G>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95000205 | |||||||
chr12:95000206 | T | A | 1 | a0001c0001t0001g0300 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.169+2533A>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95000206 | |||||||
chr12:95000209 | G | A | 1 | a0001c0001t0001g0300 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.169+2530C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95000209 | |||||||
chr12:95000210 | T | A | 1 | a0001c0001t0001g0300 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.169+2529A>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95000210 | |||||||
chr12:95000211 | G | A | 1 | a0001c0001t0001g0300 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.169+2528C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95000211 | |||||||
chr12:95000214 | G | A | 1 | a0001c0001t0001g0300 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.169+2525C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95000214 | |||||||
chr12:95000215 | T | A | 1 | a0001c0001t0001g0300 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.169+2524A>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95000215 | |||||||
chr12:95000218 | C | A | 1 | a0001c0001t0001g0300 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.169+2521G>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95000218 | |||||||
chr12:95000219 | T | A | 1 | a0001c0001t0001g0300 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.169+2520A>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95000219 | |||||||
chr12:95000220 | C | A | 1 | a0001c0001t0001g0300 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.169+2519G>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95000220 | |||||||
chr12:95000222 | G | A | 1 | a0001c0001t0001g0300 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.169+2517C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95000222 | |||||||
chr12:95000223 | G | A | 112 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(109): Show |
148 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.169+2516C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95000223 | |||||||
chr12:95000226 | T | A | 1 | a0001c0001t0001g0300 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.169+2513A>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95000226 | |||||||
chr12:95000227 | G | A | 1 | a0001c0001t0001g0300 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.169+2512C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95000227 | |||||||
chr12:95000229 | T | A | 1 | a0001c0001t0001g0300 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.169+2510A>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95000229 | |||||||
chr12:95000254 | T | C | 34 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(31): Show |
63 | HG00438.hp1 HG00438.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.169+2485A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95000254 | |||||||
chr12:95000342 | C | A | 1 | a0001c0001t0001g0221 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.169+2397G>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95000342 | |||||||
chr12:95000389 | A | C | 1 | a0001c0001t0003g0312 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.169+2350T>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95000389 | |||||||
chr12:95000478 | A | C | 26 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0026 others(23): Show |
40 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.169+2261T>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95000478 | |||||||
chr12:95000577 | G | C | 1 | a0001c0001t0001g0064 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.169+2162C>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95000577 | |||||||
chr12:95000872 | C | T | 133 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(130): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.169+1867G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95000872 | |||||||
chr12:95000990 | C | T | 1 | a0001c0001t0001g0026 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.169+1749G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95000990 | |||||||
chr12:95001286 | CA | C | 110 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(107): Show |
146 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.169+1452delT | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95001286 | |||||||
chr12:95001516 | T | A | 1 | a0001c0001t0001g0303 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.169+1223A>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95001516 | |||||||
chr12:95001538 | G | T | 244 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(241): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.169+1201C>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95001538 | |||||||
chr12:95001582 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.169+1157G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95001582 | |||||||
chr12:95001598 | A | C | 1 | a0001c0001t0001g0143 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.169+1141T>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95001598 | |||||||
chr12:95001619 | C | A | 1 | a0001c0001t0001g0055 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.169+1120G>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95001619 | |||||||
chr12:95001646 | A | C | 1 | a0001c0001t0001g0142 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.169+1093T>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95001646 | |||||||
chr12:95001714 | T | C | 1 | a0001c0001t0001g0199 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.169+1025A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95001714 | |||||||
chr12:95001768 | G | T | 1 | a0001c0001t0001g0200 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.169+971C>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95001768 | |||||||
chr12:95001799 | G | A | 72 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0010 others(69): Show |
100 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.169+940C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95001799 | |||||||
chr12:95001920 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.169+819G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95001920 | |||||||
chr12:95002168 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.169+571C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95002168 | |||||||
chr12:95002172 | T | G | 1 | a0001c0001t0001g0226 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.169+567A>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95002172 | |||||||
chr12:95002235 | T | C | 4 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(1): Show |
4 | HG02717.hp2 HG02809.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+504A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95002235 | |||||||
chr12:95002255 | T | C | 1 | a0001c0001t0001g0167 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.169+484A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95002255 | |||||||
chr12:95002269 | A | G | 2 | a0001c0001t0001g0025 a0001c0001t0001g0056 |
3 | HG00099.hp2 HG00642.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.169+470T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95002269 | |||||||
chr12:95002277 | TA | T | 3 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 |
3 | NA18953.hp1 NA19003.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.169+461delT | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95002277 | |||||||
chr12:95002351 | A | G | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(89): Show |
136 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.169+388T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95002351 | |||||||
chr12:95002424 | A | AGAGC | 281 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(278): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.169+314_169+315ins others(4): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95002424 | |||||||
chr12:95002437 | C | CA | 87 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(84): Show |
142 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.169+301dupT | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95002437 | |||||||
chr12:95002437 | C | CAA | 28 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0024 others(25): Show |
32 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.169+300_169+301dup others(2): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95002437 | |||||||
chr12:95002437 | C | CAAA | 13 | a0001c0001t0001g0025 a0001c0001t0001g0068 a0001c0001t0001g0069 others(10): Show |
14 | HG00099.hp2 HG00597.hp2 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.169+299_169+301dup others(3): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95002437 | |||||||
chr12:95002437 | CA | C | 5 | a0001c0001t0001g0032 a0001c0001t0001g0103 a0001c0001t0001g0204 others(2): Show |
6 | HG00323.hp1 HG03098.hp1 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.169+301delT | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95002437 | |||||||
chr12:95002437 | CAA | C | 7 | a0001c0001t0001g0013 a0001c0001t0001g0055 a0001c0001t0001g0101 others(4): Show |
11 | HG00140.hp1 HG01255.hp1 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.169+300_169+301del others(2): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95002437 | |||||||
chr12:95002437 | CAAA | C | 94 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0019 others(91): Show |
121 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.169+299_169+301del others(3): Show |
NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95002437 | |||||||
chr12:95002462 | A | G | 103 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(100): Show |
134 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.169+277T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95002462 | |||||||
chr12:95002468 | C | G | 281 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(278): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.169+271G>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95002468 | |||||||
chr12:95002632 | T | A | 1 | a0001c0001t0001g0226 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.169+107A>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95002632 | |||||||
chr12:95002847 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.87-26G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 1/3 | chr12 | 95002847 | |||||||
chr12:95002866 | G | T | 1 | a0001c0001t0001g0227 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.87-45C>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 1/3 | chr12 | 95002866 | |||||||
chr12:95002893 | A | T | 170 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(167): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.87-72T>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 1/3 | chr12 | 95002893 | |||||||
chr12:95003018 | C | T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.87-197G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 1/3 | chr12 | 95003018 | |||||||
chr12:95003130 | C | A | 100 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(97): Show |
131 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.87-309G>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 1/3 | chr12 | 95003130 | |||||||
chr12:95003256 | C | T | 27 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0026 others(24): Show |
41 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.86+339G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 1/3 | chr12 | 95003256 | |||||||
chr12:95003499 | G | T | 24 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(21): Show |
27 | HG00099.hp2 HG00597.hp2 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.86+96C>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 1/3 | chr12 | 95003499 |