| 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 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 145 | 442 | 90 | 78 | 208 | 18 | 46 | 166 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | copy fasta | chr12 | 94966333 | 95008697 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 438 | 439 | 90 | 78 | 205 | 18 | 46 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | copy fasta | chr12 | 94966333 | 95008697 |
| c0002 | 0/0 | 438 | 3 | 0 | 0 | 3 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | copy fasta | chr12 | 94966333 | 95008697 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 125 | 440 | 89 | 78 | 207 | 18 | 46 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | copy fasta | chr12 | 94966333 | 95008697 |
| t0002 | 0/0 | 125 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | copy fasta | chr12 | 94966333 | 95008697 |
| t0003 | 0/0 | 125 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | copy fasta | chr12 | 94966333 | 95008697 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 10 | 0 | 2 | 7 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0002 | 0/0 | 10 | 0 | 2 | 8 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0003 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0004 | 0/0 | 5 | 1 | 2 | 2 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0006 | 0/0 | 4 | 2 | 1 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0007 | 1/0 | 4 | 0 | 2 | 0 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0008 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0009 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0011 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0015 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0028 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0029 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0037 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0040 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0182 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 438 | 439 | 90 | 78 | 205 | 18 | 46 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | copy fasta | chr12 | 94966333 | 95008697 |
| a0001c0002 | 0/0 | 438 | 3 | 0 | 0 | 3 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | copy fasta | 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 | copy fasta | chr12 | 94966333 | 95008697 |
| a0001c0001t0002 | 0/0 | 562 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | copy fasta | chr12 | 94966333 | 95008697 |
| a0001c0001t0003 | 0/0 | 562 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | copy fasta | chr12 | 94966333 | 95008697 |
| a0001c0002t0001 | 0/0 | 562 | 3 | 0 | 0 | 3 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | copy fasta | chr12 | 94966333 | 95008697 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 10 | 0 | 2 | 7 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0002 | 0/0 | 10 | 0 | 2 | 8 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0003 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0004 | 0/0 | 5 | 1 | 2 | 2 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0006 | 0/0 | 4 | 2 | 1 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0007 | 1/0 | 4 | 0 | 2 | 0 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | 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 | 2 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0060 | 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 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0067 | 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 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | 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 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 1 | 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 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 | 0 | 0 | 1 | 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 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| 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 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 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 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0001t0003g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| a0001c0002t0001g0061 | 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 | g0091 | EUR | GBR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0059 | EUR | GBR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0103 | EUR | GBR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0090 | EUR | GBR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0292 | EUR | FIN | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0118 | EUR | FIN | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0105 | EUR | FIN | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | FIN | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | CHS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0345 | EAS | CHS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | CHS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | CHS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0356 | EAS | CHS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | CHS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | CHS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0303 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0355 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0344 | AMR | PUR | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0347 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0322 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0329 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | IBS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | IBS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0147 | EUR | IBS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0040 | EUR | IBS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | IBS | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0348 | AFR | ACB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | PEL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PEL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0343 | AMR | PEL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | KHV | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | KHV | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | KHV | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | ACB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PEL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | CDX | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | CDX | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | CDX | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CDX | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | ACB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PEL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0352 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0353 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0334 | AFR | ESN | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0307 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0354 | AFR | MSL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | ESN | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | ESN | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0351 | AFR | ESN | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0349 | AFR | MSL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0330 | AFR | MSL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | MSL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0350 | AFR | MSL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ESN | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ESN | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0340 | AFR | GWD | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | MSL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0341 | SAS | STU | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | STU | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0338 | SAS | BEB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | BEB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | BEB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | BEB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | BEB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | BEB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0328 | SAS | BEB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | STU | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | STU | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | BEB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | STU | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0342 | SAS | STU | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | STU | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | STU | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | STU | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0359 | AFR | YRI | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | YRI | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0358 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0357 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | LWK | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | LWK | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | LWK | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | LWK | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19055 | hp1 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0339 | AFR | YRI | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ASW | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ASW | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0135 | EUR | TSI | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0335 | EUR | TSI | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0044 | EUR | TSI | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0176 | EUR | TSI | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | GIH | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0337 | SAS | GIH | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | CLM | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | USA | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | USA | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | USA | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | USA | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | LWK | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | LWK | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0182 | REF | REF | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0007 | REF | REF | NDUFA12_chr12_94966333_95008697 | NDUFA12 | chr12 | 94966333 | 95008697 |
| 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 |
|---|
| 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 |
| 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 |
| 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 | 7 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(4): 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 | 89 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0022others(86): Show | 104 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.258-403A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94972023 | ||||||
| chr12:94972060
|
C | T | 92 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0022others(89): Show | 107 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(104): 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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0069 | 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 | a0001c0001t0001g0128 | 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 | a0001c0001t0001g0196 | 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 | a0001c0001t0001g0266 | 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 | a0001c0001t0001g0266 | 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 | a0001c0001t0001g0330 | 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 | 43 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(40): 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 | 43 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(40): 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 |
198 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(195): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): 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 | a0001c0001t0001g0123 | 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 | a0001c0001t0001g0334a0001c0001t0001g0336a0001c0001t0001g0339others(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 | 128 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(125): 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 | 136 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(133): 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 | a0001c0001t0001g0037a0001c0001t0001g0095a0001c0001t0001g0137others(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 | 40 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(37): 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 | a0001c0001t0001g0027a0001c0001t0001g0150a0001c0001t0001g0157others(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 | 115 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(112): 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 | a0001c0001t0001g0090 | 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 | a0001c0001t0001g0093 | 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 | a0001c0001t0001g0246 | 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 | 11 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0049others(8): 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 | 43 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(40): 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 | 126 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(123): 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 | 89 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0022others(86): Show | 104 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.258-2843G>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94974463 | ||||||
| chr12:94974618
|
G | A | 105 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(102): 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 | 198 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(195): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.258-3102C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94974722 | ||||||
| chr12:94974914
|
TAGTC | T | 4 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(1): Show | 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 | a0001c0001t0001g0291 | 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 | a0001c0001t0001g0155 | 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 | a0001c0001t0001g0180 | 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 | a0001c0001t0001g0131 | 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 | a0001c0001t0001g0018 | 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 | a0001c0001t0001g0354 | 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 | 4 | a0001c0001t0001g0296a0001c0001t0001g0304a0001c0001t0001g0314others(1): Show | 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 | a0001c0001t0001g0294 | 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 | 32 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(29): 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 | a0001c0001t0001g0257 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0324a0001c0001t0001g0326 | 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 | 41 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(38): 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 | a0001c0001t0001g0070 | 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 | a0001c0001t0001g0291 | 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 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0244others(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 | a0001c0001t0001g0291 | 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 | 166 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(163): Show | 201 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(198): 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 | a0001c0001t0001g0226 | 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 | 89 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0022others(86): Show | 104 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.258-4630G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94976250 | ||||||
| chr12:94976334
|
A | C | 11 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0049others(8): 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 | 11 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0049others(8): 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 | 198 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(195): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): 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 | a0001c0001t0001g0015a0001c0001t0001g0042a0001c0001t0001g0068others(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 | 32 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(29): 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 | 198 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(195): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): 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 | a0001c0001t0001g0307 | 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 | 89 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0022others(86): Show | 104 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.258-5119C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94976739 | ||||||
| chr12:94976847
|
T | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(195): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): 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 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0080others(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 | 198 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(195): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.258-5447C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94977067 | ||||||
| chr12:94977409
|
T | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(195): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): 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 | a0001c0001t0001g0068 | 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 | a0001c0001t0001g0351 | 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 | 307 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(304): Show | 371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.258-5851delT | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94977470 | ||||||
| chr12:94977482
|
A | C | 32 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(29): 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 | 124 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(121): Show | 147 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(144): 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 | a0001c0001t0001g0093 | 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 | a0001c0001t0001g0204 | 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 | 42 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(39): 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 | 198 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(195): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): 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 | a0001c0001t0001g0098a0001c0001t0001g0099 | 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 | a0001c0001t0001g0291 | 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 | a0001c0001t0001g0244a0001c0001t0001g0358 | 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 | a0001c0001t0001g0244a0001c0001t0001g0358 | 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 | 29 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0049others(26): 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 | a0001c0001t0001g0356 | 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 | a0001c0001t0001g0256a0001c0001t0001g0354 | 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 | a0001c0001t0001g0109 | 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 | a0001c0001t0001g0324a0001c0001t0001g0326a0001c0001t0001g0327 | 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 | a0001c0001t0001g0226 | 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 | a0001c0001t0001g0146 | 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 | a0001c0001t0001g0225 | 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 | 326 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(323): Show | 391 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(388): 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 | a0001c0001t0001g0152a0001c0001t0001g0221a0001c0001t0001g0228others(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 | a0001c0001t0001g0121 | 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 | 326 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(323): Show | 391 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(388): 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 | a0001c0001t0001g0229 | 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 | a0001c0002t0001g0046 | 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 | 30 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0049others(27): 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 | 92 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0022others(89): Show | 107 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.258-8048delT | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94979667 | ||||||
| chr12:94979693
|
G | T | 11 | a0001c0001t0001g0005a0001c0001t0001g0195a0001c0001t0001g0198others(8): 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 | 325 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.258-8101C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94979721 | ||||||
| chr12:94979835
|
C | CA | 149 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(146): 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 | 7 | a0001c0001t0001g0043a0001c0001t0001g0277a0001c0001t0001g0291others(4): 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 | 32 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(29): 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 | a0001c0001t0001g0250 | 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 | 7 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(4): 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 | a0001c0001t0001g0189 | 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 | a0001c0001t0001g0148a0001c0001t0001g0149 | 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 | a0001c0001t0001g0257 | 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 | 43 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(40): 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 | 325 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): 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 | a0001c0001t0001g0078 | 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 | 331 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(328): Show | 396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.258-8967delT | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94980586 | ||||||
| chr12:94980662
|
A | C | 2 | a0001c0001t0001g0256a0001c0001t0001g0354 | 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 | 29 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0049others(26): 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 | 43 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(40): 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 | a0001c0001t0001g0299 | 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 | 125 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(122): 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 | 45 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(42): 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 | a0001c0001t0001g0299 | 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 | a0001c0001t0001g0155 | 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 | 325 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.258-9585C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94981205 | ||||||
| chr12:94981269
|
A | AATAC | 183 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(180): Show | 219 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(216): 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 |
136 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(133): 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 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0209 | 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 | 325 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.258-9699C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94981319 | ||||||
| chr12:94981341
|
C | T | 43 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(40): 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 | a0001c0001t0001g0112 | 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 | 29 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0049others(26): 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 | a0001c0001t0001g0275 | 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 | a0001c0001t0001g0226 | 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 | 325 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): 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 | a0001c0001t0001g0057 | 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 | a0001c0001t0001g0112a0001c0001t0001g0152a0001c0001t0001g0221others(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 | 325 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.258-10044C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94981664 | ||||||
| chr12:94981692
|
A | G | 32 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(29): 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 | 325 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): 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 | a0001c0001t0001g0171 | 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 | 2 | a0001c0001t0001g0077a0001c0001t0001g0079 | 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 | 325 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.258-10294T>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94981914 | ||||||
| chr12:94981942
|
G | A | 29 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0049others(26): 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 | 325 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.258-10365A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94981985 | ||||||
| chr12:94981997
|
A | G | 92 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0022others(89): Show | 107 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.258-10377T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94981997 | ||||||
| chr12:94982046
|
G | A | 325 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.258-10426C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94982046 | ||||||
| chr12:94982134
|
T | C | 325 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): 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 | a0001c0001t0001g0233a0001c0001t0001g0235a0001c0001t0001g0237others(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 | 321 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(318): Show | 386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): 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 | a0001c0001t0001g0112a0001c0001t0001g0222a0001c0001t0001g0223others(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 | 5 | a0001c0001t0001g0043a0001c0001t0001g0348a0001c0001t0001g0349others(2): Show | 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 | a0001c0001t0001g0157 | 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 | 325 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): 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 | a0001c0001t0001g0334 | 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 | 2 | a0001c0001t0001g0077a0001c0001t0001g0079 | 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 | 325 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.258-11016T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94982636 | ||||||
| chr12:94982688
|
C | T | 155 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(152): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.258-11068G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94982688 | ||||||
| chr12:94982696
|
G | A | 325 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.258-11076C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94982696 | ||||||
| chr12:94982731
|
C | T | 29 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0049others(26): 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 | a0001c0001t0001g0114 | 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 | 325 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.257+10786A>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94983384 | ||||||
| chr12:94983428
|
T | C | 335 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(332): Show | 400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
intron_variant | MODIFIER | c.257+10742A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94983428 | ||||||
| chr12:94983519
|
C | T | 125 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(122): 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 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0143others(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 | 325 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.257+10578C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94983592 | ||||||
| chr12:94983714
|
T | C | 155 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(152): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.257+10456A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94983714 | ||||||
| chr12:94983736
|
C | T | 325 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.257+10434G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94983736 | ||||||
| chr12:94983767
|
GCTT | G | 325 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): 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 | a0001c0001t0001g0257 | 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 | a0001c0001t0001g0155 | 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 | a0001c0001t0001g0100 | 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 | 325 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): 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 | 325 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.257+10254C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94983916 | ||||||
| chr12:94983917
|
G | A | 325 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.257+10253C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94983917 | ||||||
| chr12:94984162
|
T | C | 170 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(167): 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 | a0001c0001t0001g0069a0001c0001t0001g0070 | 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 | a0001c0001t0001g0055 | 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 | a0001c0001t0001g0152a0001c0001t0001g0221a0001c0001t0001g0228others(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 | a0001c0001t0001g0152a0001c0001t0001g0221a0001c0001t0001g0228others(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 | 170 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(167): 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 | 325 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): 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 | a0001c0001t0001g0152a0001c0001t0001g0221a0001c0001t0001g0228others(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 | a0001c0001t0001g0219 | 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 | 325 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): 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 | a0001c0001t0001g0155 | 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 | 325 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.257+9473G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94984697 | ||||||
| chr12:94984727
|
C | A | 325 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.257+9443G>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94984727 | ||||||
| chr12:94984730
|
C | A | 325 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.257+9440G>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94984730 | ||||||
| chr12:94984736
|
A | AAAAAC | 19 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0117others(16): 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 | 76 | a0001c0001t0001g0015a0001c0001t0001g0042a0001c0001t0001g0044others(73): 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 | 183 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): 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 | 39 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(36): 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 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0175others(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 | a0001c0001t0001g0276 | 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 | a0001c0001t0001g0212 | 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 | 325 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): 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 | a0001c0001t0001g0256 | 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 | 325 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): 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 | 325 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): 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 |
168 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(165): 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 | a0001c0001t0001g0256 | 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 |
91 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0022others(88): Show | 106 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(103): 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 |
29 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0018others(26): 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 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0080others(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 |
25 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0049others(22): 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 | a0001c0001t0001g0055a0001c0001t0001g0065a0001c0001t0001g0067 | 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 | a0001c0001t0001g0148 | 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 | a0001c0001t0001g0256 | 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 | 168 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(165): 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 | 323 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(320): Show | 388 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(385): 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 | a0001c0001t0001g0148a0001c0001t0001g0149 | 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 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0209 | 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 | a0001c0001t0001g0174 | 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 | a0001c0001t0001g0018 | 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 | a0001c0001t0001g0082a0001c0001t0001g0089 | 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 | 325 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): 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 | a0001c0001t0001g0357 | 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 | a0001c0001t0001g0227 | 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 | 326 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(323): Show | 391 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(388): Show |
intron_variant | MODIFIER | c.257+8858C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94985312 | ||||||
| chr12:94985362
|
C | T | 43 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(40): 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 | a0001c0001t0001g0227 | 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 | 14 | a0001c0001t0001g0023a0001c0001t0001g0106a0001c0001t0001g0107others(11): 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 | a0001c0001t0001g0354 | 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 | a0001c0001t0001g0311 | 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 | a0001c0001t0001g0112a0001c0001t0001g0152a0001c0001t0001g0221others(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 | 325 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.257+8595A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94985575 | ||||||
| chr12:94985626
|
C | CA | 50 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0044others(47): 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 | 79 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0023others(76): Show | 92 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(89): 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 | a0001c0001t0001g0022a0001c0001t0001g0098a0001c0001t0001g0104others(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 | a0001c0001t0001g0071 | 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 | 7 | a0001c0001t0001g0124a0001c0001t0001g0127a0001c0001t0001g0128others(4): Show | 7 | HG01433.hp1 HG02004.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.257+8455T>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94985715 | ||||||
| chr12:94985777
|
G | C | 357 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(354): Show | 437 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(434): 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 | a0001c0001t0001g0050a0001c0001t0001g0052 | 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 | a0001c0002t0001g0046 | 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 | a0001c0001t0001g0087 | 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 | 7 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(4): 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 | 326 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(323): Show | 391 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(388): 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 | a0001c0001t0001g0162 | 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 | 29 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0049others(26): 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 | 336 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(333): Show | 401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.257+8144C>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94986026 | ||||||
| chr12:94986030
|
A | G | 32 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(29): 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 | a0001c0001t0001g0227 | 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 | 283 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(280): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.257+8107G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94986063 | ||||||
| chr12:94986085
|
C | CTAAA | 130 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0019others(127): Show | 145 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(142): 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 |
48 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(45): 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 | a0001c0001t0001g0221a0001c0001t0001g0230 | 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 | 45 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(42): 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 | 43 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(40): 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 | 155 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(152): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): 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 | a0001c0001t0001g0256a0001c0001t0001g0354 | 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 | a0001c0001t0001g0184 | 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 | a0001c0001t0001g0093 | 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 | 283 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(280): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.257+7676G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94986494 | ||||||
| chr12:94986531
|
T | C | 283 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(280): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.257+7639A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94986531 | ||||||
| chr12:94986564
|
T | C | 92 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0022others(89): Show | 107 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.257+7606A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94986564 | ||||||
| chr12:94986642
|
AC | A | 282 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(279): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.257+7527delG | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94986642 | ||||||
| chr12:94986643
|
C | A | 1 | a0001c0001t0001g0291 | 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 | 32 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(29): 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 | 7 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(4): 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 | 29 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0049others(26): 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 | a0001c0001t0001g0241 | 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 | 92 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0022others(89): Show | 107 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.257+7293delC | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94986876 | ||||||
| chr12:94987002
|
C | T | 1 | a0001c0001t0001g0271 | 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 | 43 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(40): 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 | a0001c0001t0001g0246 | 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 | 43 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(40): 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 | a0001c0001t0001g0226 | 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 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0143others(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 | a0001c0001t0001g0112a0001c0001t0001g0152a0001c0001t0001g0221others(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 | 283 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(280): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): 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 | a0001c0001t0001g0151 | 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 | a0001c0001t0001g0152a0001c0001t0001g0230a0001c0001t0001g0244others(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 | 200 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0009others(197): Show | 237 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.257+6378delT | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94987791 | ||||||
| chr12:94987791
|
CAA | C | 43 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(40): 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 | 31 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0049others(28): 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 | a0001c0001t0001g0157 | 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 | 42 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(39): 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 | a0001c0001t0001g0112a0001c0001t0001g0152a0001c0001t0001g0221others(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 | a0001c0001t0001g0065a0001c0001t0001g0067 | 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 | 126 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(123): 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 | 283 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(280): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): 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 | a0001c0001t0001g0143 | 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 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0209 | 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 | a0001c0001t0001g0163 | 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 | a0001c0001t0001g0274 | 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 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0310others(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 | a0001c0001t0001g0256 | 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 | 2 | a0001c0001t0001g0287a0001c0001t0001g0288 | 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 | a0001c0001t0001g0170 | 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 | 126 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(123): 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 | 43 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(40): 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 | 326 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(323): Show | 391 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(388): Show |
intron_variant | MODIFIER | c.257+5459A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94988711 | ||||||
| chr12:94988763
|
C | G | 11 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0231others(8): 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 | 155 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(152): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.257+5361G>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94988809 | ||||||
| chr12:94988825
|
C | T | 128 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(125): 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 | 43 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(40): 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 | 43 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(40): 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 | a0001c0001t0001g0103 | 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 | 43 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(40): 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 | a0001c0001t0001g0221a0001c0001t0001g0228a0001c0001t0001g0230 | 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 | 126 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(123): 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 | a0001c0001t0001g0040 | 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 | a0001c0001t0001g0134 | 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 | a0001c0001t0001g0223 | 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 | 326 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(323): Show | 391 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(388): Show |
intron_variant | MODIFIER | c.257+4231A>G | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94989939 | ||||||
| chr12:94990261
|
A | G | 105 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(102): 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 | 129 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(126): 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 | 133 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(130): Show | 168 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.257+3898delT | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94990271 | ||||||
| chr12:94990272
|
A | G | 32 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(29): 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 | 29 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0049others(26): 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 | a0001c0001t0001g0301a0001c0001t0001g0311 | 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 | 43 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(40): 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 | a0001c0001t0001g0155 | 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 | a0001c0001t0001g0341a0001c0001t0001g0342 | 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 | 92 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0022others(89): Show | 107 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(104): 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 | a0001c0001t0001g0125 | 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 | a0001c0001t0001g0100 | 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 | 336 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(333): Show | 401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): 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 | a0001c0001t0001g0112a0001c0001t0001g0222a0001c0001t0001g0223others(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 | a0001c0001t0001g0301a0001c0001t0001g0302a0001c0001t0001g0311others(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 | 43 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(40): 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 | a0001c0001t0001g0155 | 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 | a0001c0001t0001g0125 | 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 | 171 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(168): 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 | a0001c0001t0001g0112a0001c0001t0001g0142a0001c0001t0001g0146others(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 | 43 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(40): 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 | 127 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(124): 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 | a0001c0001t0001g0112a0001c0001t0001g0152a0001c0001t0001g0221others(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 | a0001c0001t0001g0169 | 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 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0209 | 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 | a0001c0001t0001g0273a0001c0001t0001g0281 | 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 | 171 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(168): 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 | 21 | a0001c0001t0001g0043a0001c0001t0001g0111a0001c0001t0001g0147others(18): 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 | a0001c0001t0001g0289 | 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 | 4 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(1): Show | 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 | a0001c0001t0001g0256 | 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 | a0001c0001t0001g0298 | 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 | a0001c0001t0001g0259 | 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 | 29 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0049others(26): 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 | 128 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(125): 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 | a0001c0001t0001g0270 | 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 | 126 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(123): 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 | a0001c0001t0001g0017 | 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 | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(166): 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 | a0001c0001t0001g0112a0001c0001t0001g0222a0001c0001t0001g0223others(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 | a0001c0001t0001g0112a0001c0001t0001g0152a0001c0001t0001g0221others(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 | a0001c0001t0001g0256 | 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 | a0001c0001t0001g0069a0001c0001t0001g0070 | 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 | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(166): 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 | 27 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0090others(24): 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 | 13 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0050others(10): 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 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0052others(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 | a0001c0001t0001g0013a0001c0001t0001g0041a0001c0001t0001g0042others(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 | 41 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(38): 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 |
30 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0231others(27): 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 | a0001c0001t0001g0317a0001c0001t0001g0323 | 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 | a0001c0001t0001g0147a0001c0001t0001g0188a0001c0001t0001g0259others(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 |
4 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0001t0001g0338others(1): Show | 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 | a0001c0001t0001g0261a0001c0001t0001g0342 | 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 | a0001c0001t0001g0351 | 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 | 99 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(96): Show | 131 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(128): 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 | a0001c0001t0001g0124 | 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 | a0001c0001t0001g0251 | 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 | a0001c0001t0001g0299 | 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 | a0001c0001t0001g0155 | 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 | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(166): 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 | 157 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(154): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.257+404G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 3/3 | chr12 | 94993766 | ||||||
| chr12:94993780
|
C | T | 126 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(123): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): 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 | a0001c0001t0001g0155 | 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 | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(166): 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 | 34 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0032others(31): 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 | 31 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(28): 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 | a0001c0001t0001g0120 | 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 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0069others(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 | 7 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(4): 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 | 103 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(100): 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 | a0001c0001t0001g0221a0001c0001t0001g0228a0001c0001t0001g0230 | 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 | 32 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(29): 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 | a0001c0001t0001g0265a0001c0001t0001g0266 | 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 | a0001c0001t0001g0256 | 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 | a0001c0001t0001g0112 | 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 | 29 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0049others(26): 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 | a0001c0001t0001g0178a0001c0001t0001g0213 | 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 | a0001c0001t0001g0178a0001c0001t0001g0213 | 2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.170-1250G>T | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94995507 | ||||||
| chr12:94995552
|
C | T | 1 | a0001c0001t0001g0182 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.170-1295G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94995552 | ||||||
| chr12:94995568
|
C | T | 11 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0049others(8): 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 | 124 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(121): 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 | a0001c0001t0001g0112a0001c0001t0001g0152a0001c0001t0001g0221others(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 | 149 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(146): 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 | 21 | a0001c0001t0001g0043a0001c0001t0001g0111a0001c0001t0001g0147others(18): 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 | a0001c0001t0001g0254 | 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 | a0001c0001t0001g0239 | 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 | 21 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(18): 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 | a0001c0001t0001g0324a0001c0001t0001g0325a0001c0001t0001g0326others(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 | 157 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(154): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.170-1980T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94996237 | ||||||
| chr12:94996324
|
T | TAC | 48 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(45): 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 | a0001c0001t0001g0013a0001c0001t0001g0040a0001c0001t0001g0224others(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 | a0001c0001t0001g0014a0001c0001t0001g0041a0001c0001t0001g0112others(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 |
28 | a0001c0001t0001g0015a0001c0001t0001g0042a0001c0001t0001g0220others(25): 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 |
20 | a0001c0001t0001g0043a0001c0001t0001g0152a0001c0001t0001g0228others(17): 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 |
12 | a0001c0001t0001g0111a0001c0001t0001g0221a0001c0001t0001g0259others(9): 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 | a0001c0001t0001g0328a0001c0001t0003g0359 | 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 | a0001c0001t0001g0223a0001c0001t0001g0339a0001c0001t0001g0340 | 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 | a0001c0001t0001g0157a0001c0001t0001g0162a0001c0001t0001g0226 | 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 |
37 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(34): 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 | a0001c0001t0001g0029a0001c0001t0001g0179 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(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 | 88 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0022others(85): Show | 103 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(100): 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 | 34 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0049others(31): 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 | 31 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(28): 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 | a0001c0001t0001g0256 | 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 | a0001c0001t0001g0354 | 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 | a0001c0001t0001g0147a0001c0001t0001g0188 | 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 | 43 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(40): 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 | a0001c0001t0001g0118a0001c0001t0001g0119 | 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 | 2 | a0001c0001t0001g0352a0001c0001t0001g0353 | 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 | a0001c0001t0001g0256a0001c0001t0001g0354 | 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 | a0001c0001t0001g0256a0001c0001t0001g0354 | 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 | 126 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(123): 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 | a0001c0001t0001g0022a0001c0001t0001g0105a0001c0001t0001g0118others(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 | a0001c0001t0001g0180 | 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 | 36 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(33): 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 | 132 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0022others(129): Show | 147 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(144): 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 | 67 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(64): 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 | a0001c0001t0001g0058 | 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 | a0001c0001t0001g0148 | 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 | 91 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0022others(88): Show | 106 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(103): 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 | a0001c0001t0001g0112a0001c0001t0001g0222a0001c0001t0001g0223others(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 | 157 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(154): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.170-2907C>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94997164 | ||||||
| chr12:94997166
|
C | T | 43 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(40): 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 | 28 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0049others(25): 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 | a0001c0001t0001g0155 | 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 | 32 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(29): 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 | a0001c0001t0001g0227 | 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 | a0001c0001t0001g0227 | 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 | 43 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(40): 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 | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(166): 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 | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(166): 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 | 43 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(40): 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 | 43 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(40): 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 | 124 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(121): 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 | 326 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(323): Show | 391 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(388): 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 | a0001c0001t0001g0331a0001c0001t0001g0332a0001c0001t0001g0333 | 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 | 103 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(100): 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 | a0001c0001t0001g0208 | 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 | 171 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(168): 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 | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(166): 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 | a0001c0001t0001g0154 | 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 | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(166): 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 | a0001c0001t0001g0160a0001c0001t0001g0161 | 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 | a0001c0001t0001g0214 | 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 | 171 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(168): 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 | 43 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0023others(40): Show | 49 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.169+3857G>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94998882 | ||||||
| chr12:94998884
|
A | G | 105 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(102): 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 | 336 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(333): Show | 401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): 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 | a0001c0001t0001g0224 | 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 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(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 | a0001c0001t0001g0155 | 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 | 157 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(154): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.169+3119G>A | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 94999620 | ||||||
| chr12:94999728
|
T | C | 7 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(4): 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 | a0001c0001t0001g0112 | 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 | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(166): 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 | a0001c0001t0001g0159 | 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 | a0001c0001t0003g0359 | 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 | 28 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0049others(25): 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 | a0001c0001t0001g0343 | 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 | a0001c0001t0001g0343 | 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 | a0001c0001t0001g0343 | 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 | a0001c0001t0001g0343 | 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 | a0001c0001t0001g0343 | 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 | 127 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(124): 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 | a0001c0001t0001g0343 | 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 | a0001c0001t0001g0343 | 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 | a0001c0001t0001g0343 | 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 | a0001c0001t0001g0343 | 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 | a0001c0001t0001g0343 | 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 | a0001c0001t0001g0343 | 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 | a0001c0001t0001g0343 | 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 | a0001c0001t0001g0343 | 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 | a0001c0001t0001g0343 | 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 | a0001c0001t0001g0343 | 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 | a0001c0001t0001g0343 | 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 | a0001c0001t0001g0343 | 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 | a0001c0001t0001g0343 | 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 | a0001c0001t0001g0343 | 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 | a0001c0001t0001g0343 | 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 | 126 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(123): 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 | a0001c0001t0001g0343 | 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 | a0001c0001t0001g0343 | 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 | a0001c0001t0001g0343 | 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 | 43 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(40): 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 | a0001c0001t0001g0251 | 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 | a0001c0001t0003g0359 | 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 | 32 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(29): 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 | a0001c0001t0001g0056 | 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 | 157 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(154): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): 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 | a0001c0001t0001g0016 | 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 | 124 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(121): 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 | a0001c0001t0001g0346 | 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 | 282 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(279): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): 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 | a0001c0001t0001g0181 | 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 | a0001c0001t0001g0157 | 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 | 2 | a0001c0001t0001g0352a0001c0001t0001g0353 | 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 | a0001c0001t0001g0156 | 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 | a0001c0001t0001g0226 | 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 | a0001c0001t0001g0227 | 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 | 86 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0022others(83): Show | 101 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(98): 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 | a0001c0001t0001g0227 | 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 | a0001c0001t0001g0256 | 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 | a0001c0001t0001g0256 | 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 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155others(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 | a0001c0001t0001g0187 | 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 | 3 | a0001c0001t0001g0044a0001c0001t0001g0059a0001c0001t0001g0060 | 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 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110 | 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 | 109 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(106): Show | 137 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.169+388T>C | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95002351 | ||||||
| chr12:95002424
|
A | AGAGC | 325 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): 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 | 107 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(104): Show | 143 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.169+301dupT | NDUFA12 | ENSG00000184752.14 | transcript | ENST00000327772.7 | protein_coding | 2/3 | chr12 | 95002437 | ||||||
| chr12:95002437
|
C | CAA | 31 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0049others(28): 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 | 14 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0062others(11): 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 | 6 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(3): 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 | 10 | a0001c0001t0001g0043a0001c0001t0001g0103a0001c0001t0001g0104others(7): 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 | 103 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0013others(100): 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 | 115 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0013others(112): 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 | 325 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): 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 | a0001c0001t0001g0256 | 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 | a0001c0001t0001g0100 | 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 | a0001c0001t0001g0257 | 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 | 202 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(199): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): 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 | a0001c0001t0001g0098a0001c0001t0001g0099 | 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 | 112 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0013others(109): 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 | 33 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(30): 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 | 27 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048others(24): 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 |