Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 137682 |
| ensemblid | ENSG00000156170.14 |
| hgncid | 28625 |
| symbol | NDUFAF6 |
| name | NADH:ubiquinone oxidoreductase complex assembly factor 6 |
| refseq_nuc | NM_152416.4 |
| refseq_prot | NP_689629.2 |
| ensembl_nuc | ENST00000396124.9 |
| ensembl_prot | ENSP00000379430.4 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 95024989 |
| end | 95058710 |
| strand | + |
| ver | v1.2 |
| region | chr8:95024989-95058710 |
| region5000 | chr8:95019989-95063710 |
| regionname0 | NDUFAF6_chr8_95024989_95058710 |
| regionname5000 | NDUFAF6_chr8_95019989_95063710 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 333 | 335 | 92 | 66 | 134 | 12 | 29 | 98 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | MAASA others(328): Show |
chr8 | 95019989 | 95063710 |
| a0002 | 0/0 | 333 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | MAASA others(328): Show |
chr8 | 95019989 | 95063710 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 999 | 328 | 86 | 65 | 134 | 12 | 29 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | ATGGC others(994): Show |
chr8 | 95019989 | 95063710 | ||
| a0001c0002 | 0/0 | 999 | 3 | 3 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | ATGGC others(994): Show |
chr8 | 95019989 | 95063710 | ||
| a0001c0003 | 0/0 | 999 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | ATGGC others(994): Show |
chr8 | 95019989 | 95063710 | ||
| a0001c0005 | 0/0 | 999 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | ATGGC others(994): Show |
chr8 | 95019989 | 95063710 | ||
| a0001c0006 | 0/0 | 999 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | ATGGC others(994): Show |
chr8 | 95019989 | 95063710 | ||
| a0001c0007 | 0/0 | 999 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | ATGGC others(994): Show |
chr8 | 95019989 | 95063710 | ||
| a0002c0004 | 0/0 | 999 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | ATGGC others(994): Show |
chr8 | 95019989 | 95063710 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1795 | 299 | 63 | 62 | 134 | 11 | 28 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | GGGCA others(1790): Show |
chr8 | 95019989 | 95063710 |
| a0001c0001t0002 | 1/0 | 1795 | 9 | 4 | 3 | 0 | 1 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | GGGCA others(1790): Show |
chr8 | 95019989 | 95063710 |
| a0001c0001t0003 | 0/0 | 1795 | 9 | 9 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | GGGCA others(1790): Show |
chr8 | 95019989 | 95063710 |
| a0001c0001t0004 | 0/0 | 1795 | 7 | 7 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | GGGCA others(1790): Show |
chr8 | 95019989 | 95063710 |
| a0001c0001t0006 | 0/0 | 1795 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | GGGCA others(1790): Show |
chr8 | 95019989 | 95063710 |
| a0001c0001t0007 | 0/0 | 1795 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | GGGCA others(1790): Show |
chr8 | 95019989 | 95063710 |
| a0001c0001t0009 | 0/0 | 1795 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | GGGCA others(1790): Show |
chr8 | 95019989 | 95063710 |
| a0001c0002t0005 | 0/0 | 1795 | 3 | 3 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | GGGCA others(1790): Show |
chr8 | 95019989 | 95063710 |
| a0001c0003t0008 | 0/0 | 1795 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | GGGCA others(1790): Show |
chr8 | 95019989 | 95063710 |
| a0001c0005t0001 | 0/0 | 1795 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | GGGCA others(1790): Show |
chr8 | 95019989 | 95063710 |
| a0001c0006t0004 | 0/0 | 1795 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | GGGCA others(1790): Show |
chr8 | 95019989 | 95063710 |
| a0001c0007t0002 | 0/0 | 1795 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | GGGCA others(1790): Show |
chr8 | 95019989 | 95063710 |
| a0002c0004t0001 | 0/0 | 1795 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | GGGCA others(1790): Show |
chr8 | 95019989 | 95063710 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 26 | 1 | 3 | 18 | 3 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0002 | 0/0 | 18 | 0 | 5 | 11 | 0 | 2 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0003 | 0/0 | 8 | 1 | 1 | 5 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0004 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0005 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0007 | 0/0 | 6 | 1 | 4 | 0 | 1 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0009 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0010 | 0/0 | 5 | 1 | 2 | 2 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 1 | 1 | 2 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0055 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0002g0135 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0003g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0006g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0007g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0001t0009g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0002t0005g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0002t0005g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0002t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0003t0008g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0005t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0006t0004g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0001c0007t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| a0002c0004t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | GBR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0133 | EUR | GBR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0091 | EUR | GBR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01261 | hp1 | a0001 | c0006 | t0004 | g0070 | AMR | CLM | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0131 | AMR | CLM | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | ACB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0132 | AMR | PEL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0125 | AFR | ACB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CDX | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CDX | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CDX | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02257 | hp1 | a0001 | c0002 | t0005 | g0076 | AFR | ACB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0126 | AFR | ACB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0062 | AFR | ACB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0047 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0046 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0039 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02818 | hp2 | a0001 | c0001 | t0007 | g0048 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0063 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0124 | AFR | ESN | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02976 | hp1 | a0001 | c0002 | t0005 | g0077 | AFR | ESN | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ESN | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0028 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03098 | hp1 | a0001 | c0007 | t0002 | g0128 | AFR | MSL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | MSL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0074 | AFR | MSL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0028 | AFR | MSL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0122 | AFR | ESN | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0073 | AFR | ESN | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03540 | hp1 | a0001 | c0002 | t0005 | g0075 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | STU | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | STU | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03710 | hp1 | a0001 | c0001 | t0009 | g0001 | SAS | PJL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03831 | hp1 | a0002 | c0004 | t0001 | g0001 | SAS | BEB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | BEB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | BEB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | BEB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | STU | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | STU | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | BEB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | STU | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | STU | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | YRI | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | YRI | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | CHB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0123 | AFR | YRI | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA19240 | hp2 | a0001 | c0003 | t0008 | g0052 | AFR | YRI | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0127 | AFR | ASW | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ASW | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0183 | EUR | TSI | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0065 | EUR | TSI | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0057 | EUR | TSI | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | GIH | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | GIH | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0129 | AFR | MSL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | USA | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| HG06807 | hp2 | a0001 | c0005 | t0001 | g0141 | AFR | USA | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | USA | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | USA | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | LWK | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0055 | REF | REF | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0135 | REF | REF | NDUFAF6_chr8_95019989_95063710 | NDUFAF6 | chr8 | 95019989 | 95063710 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:95025091 | G | C | 1 | a0002 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.83G>C | p.Gly28Ala | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/9 | 103/1795 | 83/1002 | 28/333 | chr8 | 95025091 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:95025059 | C | A | 1 | a0001c0003 | 1 | NA19240.hp2 | synonymous_variant | LOW | c.51C>A | p.Ile17Ile | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/9 | 71/1795 | 51/1002 | 17/333 | chr8 | 95025059 | |||
| chr8:95032019 | A | G | 1 | a0001c0007 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.222A>G | p.Leu74Leu | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/9 | 242/1795 | 222/1002 | 74/333 | chr8 | 95032019 | |||
| chr8:95032022 | C | T | 1 | a0001c0002 | 3 | HG02257.hp1 HG02976.hp1 HG03540.hp1 |
synonymous_variant | LOW | c.225C>T | p.Cys75Cys | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/9 | 245/1795 | 225/1002 | 75/333 | chr8 | 95032022 | |||
| chr8:95047055 | C | T | 1 | a0001c0006 | 1 | HG01261.hp1 | synonymous_variant | LOW | c.642C>T | p.Val214Val | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/9 | 662/1795 | 642/1002 | 214/333 | chr8 | 95047055 | |||
| chr8:95052209 | A | C | 1 | a0001c0005 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.852A>C | p.Ala284Ala | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/9 | 872/1795 | 852/1002 | 284/333 | chr8 | 95052209 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:95057953 | T | C | 10 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(7): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(313): Show |
3_prime_UTR_variant | MODIFIER | c.*16T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 9/9 | 16 | chr8 | 95057953 | ||||||
| chr8:95058081 | T | G | 1 | a0001c0001t0007 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*144T>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 9/9 | 144 | chr8 | 95058081 | ||||||
| chr8:95058086 | G | A | 1 | a0001c0001t0006 | 2 | HG03041.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*149G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 9/9 | 149 | chr8 | 95058086 | ||||||
| chr8:95058145 | T | C | 5 | a0001c0001t0004 a0001c0001t0007 a0001c0002t0005 others(2): Show |
13 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*208T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 9/9 | 208 | chr8 | 95058145 | ||||||
| chr8:95058246 | G | A | 1 | a0001c0001t0003 | 9 | HG02145.hp2 HG02257.hp2 HG02622.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*309G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 9/9 | 309 | chr8 | 95058246 | ||||||
| chr8:95058258 | G | A | 1 | a0001c0003t0008 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*321G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 9/9 | 321 | chr8 | 95058258 | ||||||
| chr8:95058325 | C | G | 1 | a0001c0001t0009 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*388C>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 9/9 | 388 | chr8 | 95058325 | ||||||
| chr8:95058645 | G | C | 5 | a0001c0001t0004 a0001c0001t0007 a0001c0002t0005 others(2): Show |
13 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*708G>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 9/9 | 708 | chr8 | 95058645 | ||||||
| chr8:95058687 | C | T | 1 | a0001c0002t0005 | 3 | HG02257.hp1 HG02976.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*750C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 9/9 | 750 | chr8 | 95058687 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:95025248 | CCCGGGGT others(8): Show |
C | 1 | a0001c0001t0001g0206 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.197+45_197+59delCG others(13): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr8 | 95025248 | ||||||
| chr8:95025519 | T | A | 1 | a0001c0001t0001g0020 | 2 | HG01255.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.197+314T>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95025519 | |||||||
| chr8:95025540 | A | G | 1 | a0001c0001t0001g0205 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.197+335A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95025540 | |||||||
| chr8:95025637 | T | A | 1 | a0001c0001t0001g0043 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.197+432T>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95025637 | |||||||
| chr8:95025784 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.197+579C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95025784 | |||||||
| chr8:95025844 | G | A | 29 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0021 others(26): Show |
37 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.197+639G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95025844 | |||||||
| chr8:95026024 | C | G | 97 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(94): Show |
170 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(167): Show |
intron_variant | MODIFIER | c.197+819C>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95026024 | |||||||
| chr8:95026239 | C | G | 1 | a0001c0001t0001g0069 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.197+1034C>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95026239 | |||||||
| chr8:95026245 | G | A | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(186): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.197+1040G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95026245 | |||||||
| chr8:95026338 | C | T | 5 | a0001c0001t0001g0019 a0001c0001t0001g0042 a0001c0001t0001g0201 others(2): Show |
8 | HG00621.hp1 HG02040.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.197+1133C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95026338 | |||||||
| chr8:95026492 | T | G | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG03831.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.197+1287T>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95026492 | |||||||
| chr8:95026591 | G | T | 3 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 |
3 | HG01891.hp2 HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.197+1386G>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95026591 | |||||||
| chr8:95026623 | T | C | 1 | a0001c0006t0004g0070 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.197+1418T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95026623 | |||||||
| chr8:95026731 | T | C | 29 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0021 others(26): Show |
37 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.197+1526T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95026731 | |||||||
| chr8:95026880 | G | C | 1 | a0001c0001t0001g0022 | 2 | HG01070.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.197+1675G>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95026880 | |||||||
| chr8:95026915 | G | A | 2 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
2 | HG02027.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.197+1710G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95026915 | |||||||
| chr8:95026948 | A | AG | 26 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0021 others(23): Show |
34 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.197+1745dupG | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr8 | 95026948 | ||||||
| chr8:95026988 | A | C | 1 | a0001c0001t0001g0065 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.197+1783A>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95026988 | |||||||
| chr8:95026995 | G | A | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | HG02109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.197+1790G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95026995 | |||||||
| chr8:95027019 | T | C | 29 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0021 others(26): Show |
37 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.197+1814T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95027019 | |||||||
| chr8:95027158 | C | T | 1 | a0001c0001t0007g0048 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.197+1953C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95027158 | |||||||
| chr8:95027163 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.197+1958C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95027163 | |||||||
| chr8:95027269 | T | C | 5 | a0001c0001t0004g0073 a0001c0001t0004g0074 a0001c0002t0005g0075 others(2): Show |
5 | HG02257.hp1 HG02976.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.197+2064T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95027269 | |||||||
| chr8:95027579 | C | CA | 27 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0021 others(24): Show |
35 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.197+2393dupA | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr8 | 95027579 | ||||||
| chr8:95027579 | C | CAA | 7 | a0001c0001t0001g0044 a0001c0001t0001g0049 a0001c0001t0001g0050 others(4): Show |
7 | HG01891.hp2 HG01981.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.197+2392_197+2393d others(4): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr8 | 95027579 | ||||||
| chr8:95027579 | CA | C | 7 | a0001c0001t0001g0041 a0001c0001t0001g0119 a0001c0001t0001g0120 others(4): Show |
8 | HG03710.hp2 NA18981.hp1 NA18986.hp2 others(5): Show |
intron_variant | MODIFIER | c.197+2393delA | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr8 | 95027579 | ||||||
| chr8:95027712 | A | T | 1 | a0001c0001t0004g0063 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.197+2507A>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95027712 | |||||||
| chr8:95027866 | C | T | 2 | a0001c0001t0004g0046 a0001c0001t0004g0047 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.197+2661C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95027866 | |||||||
| chr8:95028229 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.197+3024T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95028229 | |||||||
| chr8:95028489 | T | C | 1 | a0001c0001t0001g0013 | 3 | HG02080.hp2 HG02523.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.197+3284T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95028489 | |||||||
| chr8:95028659 | A | G | 30 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0021 others(27): Show |
38 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.198-3336A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95028659 | |||||||
| chr8:95028804 | A | G | 7 | a0001c0001t0001g0026 a0001c0001t0001g0113 a0001c0001t0001g0114 others(4): Show |
8 | HG00438.hp1 HG02155.hp1 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.198-3191A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95028804 | |||||||
| chr8:95028967 | C | A | 1 | a0001c0005t0001g0141 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.198-3028C>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95028967 | |||||||
| chr8:95029022 | G | A | 29 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0021 others(26): Show |
37 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.198-2973G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95029022 | |||||||
| chr8:95029039 | A | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(186): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.198-2956A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95029039 | |||||||
| chr8:95029132 | A | C | 2 | a0001c0001t0001g0040 a0001c0001t0001g0195 |
3 | HG03654.hp2 HG03927.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.198-2863A>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95029132 | |||||||
| chr8:95029209 | G | A | 29 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0021 others(26): Show |
37 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.198-2786G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95029209 | |||||||
| chr8:95029262 | T | C | 2 | a0001c0001t0004g0046 a0001c0001t0004g0047 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.198-2733T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95029262 | |||||||
| chr8:95029372 | AT | A | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(200): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.198-2617delT | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr8 | 95029372 | ||||||
| chr8:95029416 | A | G | 21 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0013 others(18): Show |
46 | HG00609.hp2 HG00639.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.198-2579A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95029416 | |||||||
| chr8:95029518 | T | C | 29 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0021 others(26): Show |
37 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.198-2477T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95029518 | |||||||
| chr8:95029556 | A | C | 1 | a0001c0001t0001g0068 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.198-2439A>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95029556 | |||||||
| chr8:95029606 | C | T | 5 | a0001c0001t0004g0073 a0001c0001t0004g0074 a0001c0002t0005g0075 others(2): Show |
5 | HG02257.hp1 HG02976.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.198-2389C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95029606 | |||||||
| chr8:95029954 | G | A | 2 | a0001c0001t0004g0046 a0001c0001t0004g0047 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.198-2041G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95029954 | |||||||
| chr8:95030214 | A | ATTAT | 10 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0099 others(7): Show |
16 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.198-1754_198-1751d others(6): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr8 | 95030214 | ||||||
| chr8:95030214 | A | ATTATTTA others(9): Show |
2 | a0001c0001t0004g0046 a0001c0001t0004g0047 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.198-1766_198-1751d others(18): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr8 | 95030214 | ||||||
| chr8:95030314 | C | T | 1 | a0001c0006t0004g0070 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.198-1681C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95030314 | |||||||
| chr8:95030535 | T | C | 3 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0054 |
3 | HG02280.hp2 HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.198-1460T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95030535 | |||||||
| chr8:95030662 | A | G | 29 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0021 others(26): Show |
37 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.198-1333A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95030662 | |||||||
| chr8:95030960 | A | G | 29 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0021 others(26): Show |
37 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.198-1035A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95030960 | |||||||
| chr8:95030993 | T | G | 5 | a0001c0001t0004g0073 a0001c0001t0004g0074 a0001c0002t0005g0075 others(2): Show |
5 | HG02257.hp1 HG02976.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.198-1002T>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95030993 | |||||||
| chr8:95031020 | T | C | 1 | a0001c0001t0001g0205 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.198-975T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95031020 | |||||||
| chr8:95031148 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.198-847G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95031148 | |||||||
| chr8:95031151 | C | G | 1 | a0001c0006t0004g0070 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.198-844C>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95031151 | |||||||
| chr8:95031371 | C | T | 6 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 others(3): Show |
6 | HG01891.hp2 HG02258.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.198-624C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95031371 | |||||||
| chr8:95031474 | A | T | 1 | a0001c0001t0001g0068 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.198-521A>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95031474 | |||||||
| chr8:95031487 | A | C | 1 | a0001c0001t0001g0194 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.198-508A>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95031487 | |||||||
| chr8:95031552 | G | A | 5 | a0001c0001t0001g0029 a0001c0001t0001g0143 a0001c0001t0001g0144 others(2): Show |
6 | HG00642.hp1 HG01168.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.198-443G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95031552 | |||||||
| chr8:95031601 | G | A | 29 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0021 others(26): Show |
37 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.198-394G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95031601 | |||||||
| chr8:95031712 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.198-283G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95031712 | |||||||
| chr8:95031814 | T | C | 26 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0021 others(23): Show |
34 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.198-181T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95031814 | |||||||
| chr8:95031820 | C | CG | 5 | a0001c0001t0004g0073 a0001c0001t0004g0074 a0001c0002t0005g0075 others(2): Show |
5 | HG02257.hp1 HG02976.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.198-174dupG | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr8 | 95031820 | ||||||
| chr8:95031838 | T | C | 1 | a0001c0001t0004g0074 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.198-157T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95031838 | |||||||
| chr8:95031848 | G | A | 20 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0021 others(17): Show |
28 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.198-147G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95031848 | |||||||
| chr8:95031876 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.198-119C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95031876 | |||||||
| chr8:95031880 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.198-115C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95031880 | |||||||
| chr8:95031892 | C | T | 1 | a0001c0001t0007g0048 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.198-103C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95031892 | |||||||
| chr8:95031893 | G | A | 4 | a0001c0001t0001g0148 a0001c0001t0004g0062 a0001c0001t0004g0063 others(1): Show |
4 | HG02258.hp1 HG02886.hp1 NA19087.hp2 others(1): Show |
intron_variant | MODIFIER | c.198-102G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 1/8 | chr8 | 95031893 | |||||||
| chr8:95032155 | T | A | 2 | a0001c0001t0001g0040 a0001c0001t0001g0195 |
3 | HG03654.hp2 HG03927.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.297+61T>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95032155 | |||||||
| chr8:95032186 | A | T | 5 | a0001c0001t0004g0073 a0001c0001t0004g0074 a0001c0002t0005g0075 others(2): Show |
5 | HG02257.hp1 HG02976.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.297+92A>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95032186 | |||||||
| chr8:95032739 | A | C | 26 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0021 others(23): Show |
34 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.297+645A>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95032739 | |||||||
| chr8:95032841 | A | G | 3 | a0001c0001t0002g0129 a0001c0001t0002g0130 a0001c0001t0006g0028 |
4 | HG01884.hp1 HG03041.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.297+747A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95032841 | |||||||
| chr8:95032909 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.297+815C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95032909 | |||||||
| chr8:95033171 | T | C | 20 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0021 others(17): Show |
28 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.297+1077T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95033171 | |||||||
| chr8:95033213 | A | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.297+1119A>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95033213 | |||||||
| chr8:95033235 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.297+1141G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95033235 | |||||||
| chr8:95033245 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.297+1151A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95033245 | |||||||
| chr8:95033332 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.297+1238C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95033332 | |||||||
| chr8:95033341 | G | C | 58 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(55): Show |
97 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.297+1247G>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95033341 | |||||||
| chr8:95033354 | T | G | 2 | a0001c0001t0004g0046 a0001c0001t0004g0047 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.297+1260T>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95033354 | |||||||
| chr8:95033725 | G | T | 1 | a0001c0001t0001g0192 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.297+1631G>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95033725 | |||||||
| chr8:95033784 | G | A | 3 | a0001c0001t0001g0138 a0001c0001t0001g0152 a0001c0001t0001g0153 |
3 | HG02965.hp1 HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.298-1670G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95033784 | |||||||
| chr8:95033866 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
266 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.298-1588G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95033866 | |||||||
| chr8:95034140 | A | G | 1 | a0001c0006t0004g0070 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.298-1314A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95034140 | |||||||
| chr8:95034261 | T | C | 1 | a0001c0006t0004g0070 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.298-1193T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95034261 | |||||||
| chr8:95034265 | G | A | 5 | a0001c0001t0004g0073 a0001c0001t0004g0074 a0001c0002t0005g0075 others(2): Show |
5 | HG02257.hp1 HG02976.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.298-1189G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95034265 | |||||||
| chr8:95034265 | G | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
266 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.298-1189G>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95034265 | |||||||
| chr8:95034405 | C | G | 3 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0003t0008g0052 |
3 | HG02258.hp1 HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.298-1049C>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95034405 | |||||||
| chr8:95034458 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.298-996G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95034458 | |||||||
| chr8:95034459 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.298-995G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95034459 | |||||||
| chr8:95034625 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.298-829T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95034625 | |||||||
| chr8:95034650 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.298-804G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95034650 | |||||||
| chr8:95034654 | T | C | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0194 |
5 | HG02486.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.298-800T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95034654 | |||||||
| chr8:95034694 | A | T | 2 | a0001c0001t0004g0046 a0001c0001t0004g0047 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.298-760A>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95034694 | |||||||
| chr8:95034723 | A | G | 20 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0021 others(17): Show |
28 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.298-731A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95034723 | |||||||
| chr8:95034823 | C | A | 1 | a0001c0001t0001g0100 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.298-631C>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95034823 | |||||||
| chr8:95034825 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.298-629A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95034825 | |||||||
| chr8:95034839 | G | C | 5 | a0001c0001t0004g0073 a0001c0001t0004g0074 a0001c0002t0005g0075 others(2): Show |
5 | HG02257.hp1 HG02976.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.298-615G>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95034839 | |||||||
| chr8:95034967 | C | T | 4 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0003t0008g0052 others(1): Show |
4 | HG01261.hp1 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.298-487C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95034967 | |||||||
| chr8:95035020 | C | G | 3 | a0001c0002t0005g0075 a0001c0002t0005g0076 a0001c0002t0005g0077 |
3 | HG02257.hp1 HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.298-434C>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95035020 | |||||||
| chr8:95035040 | C | T | 8 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0073 others(5): Show |
8 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.298-414C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95035040 | |||||||
| chr8:95035069 | C | T | 4 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0003t0008g0052 others(1): Show |
4 | HG01261.hp1 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.298-385C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95035069 | |||||||
| chr8:95035081 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.298-373A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95035081 | |||||||
| chr8:95035242 | CTT | C | 20 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0021 others(17): Show |
28 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.298-211_298-210del others(2): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95035242 | |||||||
| chr8:95035380 | A | G | 8 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0073 others(5): Show |
8 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.298-74A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95035380 | |||||||
| chr8:95035393 | G | C | 20 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0021 others(17): Show |
28 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.298-61G>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 2/8 | chr8 | 95035393 | |||||||
| chr8:95035578 | T | TA | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.420+15dupA | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 95035578 | ||||||
| chr8:95035578 | T | TAA | 14 | a0001c0001t0001g0071 a0001c0001t0001g0148 a0001c0001t0001g0156 others(11): Show |
14 | HG01081.hp1 HG02027.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.420+14_420+15dupAA | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 95035578 | ||||||
| chr8:95035655 | T | G | 2 | a0001c0001t0004g0046 a0001c0001t0004g0047 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.420+79T>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95035655 | |||||||
| chr8:95035705 | C | G | 20 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0021 others(17): Show |
28 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.420+129C>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95035705 | |||||||
| chr8:95035880 | A | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0191 |
4 | HG00642.hp2 HG01074.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.420+304A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95035880 | |||||||
| chr8:95035906 | TCTGCCTA others(7): Show |
T | 4 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0003t0008g0052 others(1): Show |
4 | HG01261.hp1 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.420+333_420+346del others(14): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 95035906 | ||||||
| chr8:95036541 | A | G | 1 | a0001c0006t0004g0070 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.420+965A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95036541 | |||||||
| chr8:95036609 | C | T | 1 | a0001c0001t0001g0025 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.420+1033C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95036609 | |||||||
| chr8:95036618 | C | T | 8 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0073 others(5): Show |
8 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.420+1042C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95036618 | |||||||
| chr8:95036689 | T | G | 4 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0003t0008g0052 others(1): Show |
4 | HG01261.hp1 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.420+1113T>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95036689 | |||||||
| chr8:95036712 | T | C | 11 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 others(8): Show |
11 | HG01891.hp2 HG02257.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.420+1136T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95036712 | |||||||
| chr8:95036805 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.420+1229A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95036805 | |||||||
| chr8:95036838 | T | C | 4 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0003t0008g0052 others(1): Show |
4 | HG01261.hp1 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.420+1262T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95036838 | |||||||
| chr8:95036892 | A | G | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.420+1316A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95036892 | |||||||
| chr8:95036948 | C | T | 5 | a0001c0001t0004g0073 a0001c0001t0004g0074 a0001c0002t0005g0075 others(2): Show |
5 | HG02257.hp1 HG02976.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.420+1372C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95036948 | |||||||
| chr8:95037014 | T | G | 4 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0003t0008g0052 others(1): Show |
4 | HG01261.hp1 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.420+1438T>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95037014 | |||||||
| chr8:95037111 | T | C | 60 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(57): Show |
99 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.420+1535T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95037111 | |||||||
| chr8:95037329 | C | T | 3 | a0001c0001t0001g0039 a0001c0001t0001g0190 a0001c0001t0004g0039 |
3 | HG01081.hp2 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.420+1753C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95037329 | |||||||
| chr8:95037369 | T | C | 1 | a0001c0001t0007g0048 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.420+1793T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95037369 | |||||||
| chr8:95037456 | C | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
266 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.420+1880C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95037456 | |||||||
| chr8:95037550 | C | G | 3 | a0001c0001t0001g0041 a0001c0001t0001g0198 a0001c0001t0001g0199 |
4 | NA18981.hp1 NA18999.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.420+1974C>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95037550 | |||||||
| chr8:95037656 | C | T | 8 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0073 others(5): Show |
8 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.420+2080C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95037656 | |||||||
| chr8:95037774 | G | A | 12 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0062 others(9): Show |
12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.420+2198G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95037774 | |||||||
| chr8:95037896 | A | G | 1 | a0001c0001t0001g0189 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.420+2320A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95037896 | |||||||
| chr8:95038032 | C | T | 2 | a0001c0001t0001g0041 a0001c0001t0001g0199 |
3 | NA18981.hp1 NA18999.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.420+2456C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95038032 | |||||||
| chr8:95038033 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.420+2457G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95038033 | |||||||
| chr8:95038058 | A | T | 3 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0158 |
12 | HG01167.hp1 HG01891.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.420+2482A>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95038058 | |||||||
| chr8:95038059 | T | A | 8 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0073 others(5): Show |
8 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.420+2483T>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95038059 | |||||||
| chr8:95038167 | A | G | 12 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0062 others(9): Show |
12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.420+2591A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95038167 | |||||||
| chr8:95038272 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.420+2696A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95038272 | |||||||
| chr8:95038311 | G | T | 10 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0073 others(7): Show |
10 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.420+2735G>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95038311 | |||||||
| chr8:95038329 | T | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(85): Show |
152 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.420+2753T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95038329 | |||||||
| chr8:95038654 | T | C | 2 | a0001c0001t0001g0136 a0001c0001t0001g0149 |
2 | HG02109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.421-2916T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95038654 | |||||||
| chr8:95038690 | C | T | 1 | a0001c0001t0007g0048 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.421-2880C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95038690 | |||||||
| chr8:95038722 | A | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(186): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.421-2848A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95038722 | |||||||
| chr8:95038806 | T | C | 1 | a0001c0001t0003g0122 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.421-2764T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95038806 | |||||||
| chr8:95038826 | T | C | 4 | a0001c0001t0001g0021 a0001c0001t0001g0049 a0001c0001t0001g0056 others(1): Show |
5 | NA18948.hp1 NA18950.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.421-2744T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95038826 | |||||||
| chr8:95038905 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.421-2665G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95038905 | |||||||
| chr8:95038920 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.421-2650C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95038920 | |||||||
| chr8:95038959 | G | A | 6 | a0001c0001t0001g0014 a0001c0001t0001g0081 a0001c0001t0001g0082 others(3): Show |
8 | HG00639.hp1 HG00741.hp2 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.421-2611G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95038959 | |||||||
| chr8:95038983 | G | GT | 31 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0026 others(28): Show |
36 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.421-2576dupT | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 95038983 | ||||||
| chr8:95038984 | T | G | 8 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0073 others(5): Show |
8 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.421-2586T>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95038984 | |||||||
| chr8:95038986 | T | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0042 a0001c0001t0001g0201 |
6 | HG00621.hp1 NA18747.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.421-2584T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95038986 | |||||||
| chr8:95039121 | T | C | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(186): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.421-2449T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95039121 | |||||||
| chr8:95039326 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.421-2244G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95039326 | |||||||
| chr8:95039377 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.421-2193G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95039377 | |||||||
| chr8:95039462 | A | G | 1 | a0001c0001t0001g0013 | 3 | HG02080.hp2 HG02523.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.421-2108A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95039462 | |||||||
| chr8:95039463 | A | C | 3 | a0001c0001t0002g0121 a0001c0001t0002g0127 a0001c0007t0002g0128 |
3 | HG01109.hp2 HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.421-2107A>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95039463 | |||||||
| chr8:95039463 | A | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
266 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.421-2107A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95039463 | |||||||
| chr8:95039471 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.421-2099T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95039471 | |||||||
| chr8:95039533 | C | G | 4 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0003t0008g0052 others(1): Show |
4 | HG01261.hp1 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.421-2037C>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95039533 | |||||||
| chr8:95039567 | C | T | 1 | a0001c0001t0007g0048 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.421-2003C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95039567 | |||||||
| chr8:95039572 | C | T | 5 | a0001c0001t0003g0012 a0001c0001t0003g0122 a0001c0001t0003g0124 others(2): Show |
8 | HG02145.hp2 HG02257.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.421-1998C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95039572 | |||||||
| chr8:95039627 | T | TA | 3 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 |
3 | HG01891.hp2 HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.421-1942dupA | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 95039627 | ||||||
| chr8:95039822 | A | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
266 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.421-1748A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95039822 | |||||||
| chr8:95039824 | G | A | 1 | a0001c0001t0002g0129 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.421-1746G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95039824 | |||||||
| chr8:95039840 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.421-1730T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95039840 | |||||||
| chr8:95039924 | C | T | 1 | a0001c0006t0004g0070 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.421-1646C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95039924 | |||||||
| chr8:95040086 | T | A | 12 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0062 others(9): Show |
12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.421-1484T>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95040086 | |||||||
| chr8:95040174 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.421-1396G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95040174 | |||||||
| chr8:95040174 | G | C | 12 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0062 others(9): Show |
12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.421-1396G>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95040174 | |||||||
| chr8:95040193 | A | G | 1 | a0001c0001t0004g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.421-1377A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95040193 | |||||||
| chr8:95040504 | A | G | 2 | a0001c0001t0004g0046 a0001c0001t0004g0047 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.421-1066A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95040504 | |||||||
| chr8:95040659 | G | GT | 5 | a0001c0001t0004g0073 a0001c0001t0004g0074 a0001c0002t0005g0075 others(2): Show |
5 | HG02257.hp1 HG02976.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.421-905dupT | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 95040659 | ||||||
| chr8:95040692 | A | C | 1 | a0001c0001t0001g0084 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.421-878A>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95040692 | |||||||
| chr8:95040727 | G | A | 9 | a0001c0001t0001g0161 a0001c0001t0004g0046 a0001c0001t0004g0047 others(6): Show |
9 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.421-843G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95040727 | |||||||
| chr8:95040861 | G | A | 12 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0062 others(9): Show |
12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.421-709G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95040861 | |||||||
| chr8:95041009 | A | T | 8 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0073 others(5): Show |
8 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.421-561A>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95041009 | |||||||
| chr8:95041074 | C | T | 1 | a0001c0001t0001g0095 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.421-496C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95041074 | |||||||
| chr8:95041159 | G | A | 1 | a0001c0001t0001g0057 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.421-411G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95041159 | |||||||
| chr8:95041230 | A | T | 1 | a0001c0001t0001g0100 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.421-340A>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95041230 | |||||||
| chr8:95041263 | C | T | 12 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0062 others(9): Show |
12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.421-307C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95041263 | |||||||
| chr8:95041380 | A | T | 1 | a0001c0001t0001g0157 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.421-190A>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | chr8 | 95041380 | |||||||
| chr8:95041554 | GCT | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
266 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.421-13_421-12delCT | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 95041554 | ||||||
| chr8:95041772 | C | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(84): Show |
151 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.477+146C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95041772 | |||||||
| chr8:95041790 | C | T | 2 | a0001c0001t0001g0040 a0001c0001t0001g0195 |
3 | HG03654.hp2 HG03927.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.477+164C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95041790 | |||||||
| chr8:95041820 | A | C | 12 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0062 others(9): Show |
12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.477+194A>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95041820 | |||||||
| chr8:95041866 | T | G | 1 | a0001c0006t0004g0070 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.477+240T>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95041866 | |||||||
| chr8:95042036 | A | G | 3 | a0001c0001t0002g0121 a0001c0001t0002g0127 a0001c0007t0002g0128 |
3 | HG01109.hp2 HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.477+410A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95042036 | |||||||
| chr8:95042088 | C | T | 3 | a0001c0001t0003g0012 a0001c0001t0003g0122 a0001c0001t0003g0126 |
6 | HG02257.hp2 HG02622.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.477+462C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95042088 | |||||||
| chr8:95042160 | G | T | 2 | a0001c0001t0001g0041 a0001c0001t0001g0199 |
3 | NA18981.hp1 NA18999.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.477+534G>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95042160 | |||||||
| chr8:95042188 | T | C | 1 | a0001c0001t0004g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.477+562T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95042188 | |||||||
| chr8:95042381 | G | A | 5 | a0001c0001t0004g0073 a0001c0001t0004g0074 a0001c0002t0005g0075 others(2): Show |
5 | HG02257.hp1 HG02976.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.477+755G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95042381 | |||||||
| chr8:95042765 | C | T | 12 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0062 others(9): Show |
12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.477+1139C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95042765 | |||||||
| chr8:95042920 | C | A | 12 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0062 others(9): Show |
12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.477+1294C>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95042920 | |||||||
| chr8:95043086 | C | CT | 17 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0021 others(14): Show |
28 | HG00544.hp2 HG00735.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.477+1477dupT | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr8 | 95043086 | ||||||
| chr8:95043086 | CT | C | 12 | a0001c0001t0001g0088 a0001c0001t0001g0101 a0001c0001t0001g0102 others(9): Show |
12 | HG01168.hp1 HG01168.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.477+1477delT | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr8 | 95043086 | ||||||
| chr8:95043086 | CTT | C | 7 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0073 others(4): Show |
7 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.477+1476_477+1477d others(4): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr8 | 95043086 | ||||||
| chr8:95043153 | C | T | 3 | a0001c0001t0001g0018 a0001c0001t0001g0183 a0001c0001t0001g0191 |
5 | HG00642.hp2 HG01074.hp1 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.477+1527C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95043153 | |||||||
| chr8:95043170 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.477+1544C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95043170 | |||||||
| chr8:95043194 | C | A | 1 | a0001c0006t0004g0070 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.477+1568C>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95043194 | |||||||
| chr8:95043194 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.477+1568C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95043194 | |||||||
| chr8:95043245 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0027 |
5 | HG02055.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.477+1619C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95043245 | |||||||
| chr8:95043246 | G | A | 3 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0133 |
3 | HG00140.hp1 HG01496.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.477+1620G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95043246 | |||||||
| chr8:95043251 | AT | A | 12 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0062 others(9): Show |
12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.477+1637delT | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr8 | 95043251 | ||||||
| chr8:95043306 | G | T | 1 | a0001c0001t0001g0102 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.477+1680G>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95043306 | |||||||
| chr8:95043336 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.477+1710G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95043336 | |||||||
| chr8:95043373 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.477+1747G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95043373 | |||||||
| chr8:95043458 | GA | G | 20 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0021 others(17): Show |
28 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.477+1839delA | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr8 | 95043458 | ||||||
| chr8:95043476 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.477+1850G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95043476 | |||||||
| chr8:95043481 | A | G | 59 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(56): Show |
98 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.477+1855A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95043481 | |||||||
| chr8:95043519 | ACT | A | 4 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0003t0008g0052 others(1): Show |
4 | HG01261.hp1 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.477+1896_477+1897d others(4): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr8 | 95043519 | ||||||
| chr8:95043534 | G | C | 12 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0062 others(9): Show |
12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.477+1908G>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95043534 | |||||||
| chr8:95043548 | T | C | 12 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0062 others(9): Show |
12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.477+1922T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95043548 | |||||||
| chr8:95043972 | G | A | 2 | a0001c0001t0004g0046 a0001c0001t0004g0047 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.478-1573G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95043972 | |||||||
| chr8:95044224 | G | T | 1 | a0001c0001t0001g0061 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.478-1321G>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95044224 | |||||||
| chr8:95044225 | G | T | 8 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0003g0012 others(5): Show |
14 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.478-1320G>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95044225 | |||||||
| chr8:95044388 | A | G | 3 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0003t0008g0052 |
3 | HG02258.hp1 HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.478-1157A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95044388 | |||||||
| chr8:95044451 | C | CT | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(165): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.478-1076dupT | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr8 | 95044451 | ||||||
| chr8:95044451 | C | CTT | 13 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0102 others(10): Show |
22 | HG01167.hp1 HG01433.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.478-1077_478-1076d others(4): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr8 | 95044451 | ||||||
| chr8:95044508 | A | G | 6 | a0001c0001t0004g0073 a0001c0001t0004g0074 a0001c0001t0007g0048 others(3): Show |
6 | HG02257.hp1 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.478-1037A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95044508 | |||||||
| chr8:95044577 | C | G | 1 | a0001c0001t0001g0066 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.478-968C>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95044577 | |||||||
| chr8:95044577 | C | T | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(156): Show |
271 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.478-968C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95044577 | |||||||
| chr8:95044685 | A | G | 2 | a0001c0001t0001g0067 a0001c0001t0001g0068 |
2 | HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.478-860A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95044685 | |||||||
| chr8:95044693 | T | C | 8 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0073 others(5): Show |
8 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-852T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95044693 | |||||||
| chr8:95044707 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.478-838C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95044707 | |||||||
| chr8:95044745 | C | T | 3 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0003t0008g0052 |
3 | HG02258.hp1 HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.478-800C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95044745 | |||||||
| chr8:95044757 | CT | C | 13 | a0001c0001t0001g0006 a0001c0001t0001g0069 a0001c0001t0001g0089 others(10): Show |
19 | HG00544.hp1 HG01070.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.478-774delT | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr8 | 95044757 | ||||||
| chr8:95044796 | C | T | 1 | a0001c0001t0007g0048 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.478-749C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95044796 | |||||||
| chr8:95044856 | T | C | 4 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0003t0008g0052 others(1): Show |
4 | HG01261.hp1 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.478-689T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95044856 | |||||||
| chr8:95044888 | C | T | 8 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0073 others(5): Show |
8 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-657C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95044888 | |||||||
| chr8:95044962 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.478-583A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95044962 | |||||||
| chr8:95045065 | T | TC | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
266 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.478-477dupC | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr8 | 95045065 | ||||||
| chr8:95045068 | C | T | 1 | a0001c0001t0007g0048 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.478-477C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95045068 | |||||||
| chr8:95045137 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.478-408A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95045137 | |||||||
| chr8:95045179 | G | A | 5 | a0001c0001t0001g0019 a0001c0001t0001g0042 a0001c0001t0001g0201 others(2): Show |
8 | HG00621.hp1 HG02040.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.478-366G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95045179 | |||||||
| chr8:95045179 | G | T | 34 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0015 others(31): Show |
45 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.478-366G>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95045179 | |||||||
| chr8:95045221 | C | T | 7 | a0001c0001t0001g0107 a0001c0001t0001g0165 a0001c0001t0004g0073 others(4): Show |
7 | HG01256.hp2 HG02257.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.478-324C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95045221 | |||||||
| chr8:95045229 | C | G | 1 | a0001c0003t0008g0052 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.478-316C>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95045229 | |||||||
| chr8:95045253 | G | A | 12 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0062 others(9): Show |
12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.478-292G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95045253 | |||||||
| chr8:95045297 | A | T | 6 | a0001c0001t0001g0145 a0001c0001t0004g0062 a0001c0001t0004g0063 others(3): Show |
6 | HG00642.hp1 HG01261.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.478-248A>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95045297 | |||||||
| chr8:95045329 | A | T | 1 | a0001c0001t0004g0063 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.478-216A>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 4/8 | chr8 | 95045329 | |||||||
| chr8:95045722 | T | C | 12 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0062 others(9): Show |
12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.580+75T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | chr8 | 95045722 | |||||||
| chr8:95045770 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.580+123G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | chr8 | 95045770 | |||||||
| chr8:95045776 | G | GTT | 12 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0062 others(9): Show |
12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.580+136_580+137dup others(2): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr8 | 95045776 | ||||||
| chr8:95045990 | G | A | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.580+343G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | chr8 | 95045990 | |||||||
| chr8:95046022 | A | C | 1 | a0001c0001t0001g0085 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.580+375A>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | chr8 | 95046022 | |||||||
| chr8:95046032 | A | ATTTATTT others(3): Show |
1 | a0001c0001t0001g0178 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.580+408_580+417dup others(10): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr8 | 95046032 | ||||||
| chr8:95046032 | A | ATTTATTT others(9): Show |
1 | a0001c0001t0004g0073 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.580+388_580+403dup others(16): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr8 | 95046032 | ||||||
| chr8:95046032 | A | ATTTATTT others(18): Show |
1 | a0001c0001t0004g0046 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.580+393_580+417dup others(25): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr8 | 95046032 | ||||||
| chr8:95046032 | A | ATTTATTT others(23): Show |
1 | a0001c0001t0004g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.580+388_580+417dup others(30): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr8 | 95046032 | ||||||
| chr8:95046036 | A | ATTTTATT others(9): Show |
3 | a0001c0001t0004g0062 a0001c0003t0008g0052 a0001c0006t0004g0070 |
3 | HG01261.hp1 HG02258.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.580+393_580+408dup others(16): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr8 | 95046036 | ||||||
| chr8:95046036 | A | ATTTTATT others(9): Show |
4 | a0001c0001t0004g0074 a0001c0002t0005g0075 a0001c0002t0005g0076 others(1): Show |
4 | HG02257.hp1 HG02976.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.580+403_580+404ins others(16): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr8 | 95046036 | ||||||
| chr8:95046051 | A | T | 1 | a0001c0001t0007g0048 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.580+404A>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | chr8 | 95046051 | |||||||
| chr8:95046060 | T | A | 2 | a0001c0001t0002g0131 a0001c0001t0002g0132 |
2 | HG01496.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.580+413T>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | chr8 | 95046060 | |||||||
| chr8:95046061 | A | ATTTTATT others(13): Show |
1 | a0001c0001t0007g0048 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.580+417_580+418ins others(20): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr8 | 95046061 | ||||||
| chr8:95046120 | G | A | 4 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0003t0008g0052 others(1): Show |
4 | HG01261.hp1 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.580+473G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | chr8 | 95046120 | |||||||
| chr8:95046122 | T | A | 4 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0003t0008g0052 others(1): Show |
4 | HG01261.hp1 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.580+475T>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | chr8 | 95046122 | |||||||
| chr8:95046124 | A | G | 4 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0003t0008g0052 others(1): Show |
4 | HG01261.hp1 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.580+477A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | chr8 | 95046124 | |||||||
| chr8:95046125 | A | G | 6 | a0001c0001t0001g0066 a0001c0001t0004g0073 a0001c0001t0004g0074 others(3): Show |
6 | HG01891.hp2 HG02257.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.580+478A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | chr8 | 95046125 | |||||||
| chr8:95046215 | C | T | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | HG00735.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.580+568C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | chr8 | 95046215 | |||||||
| chr8:95046324 | C | T | 3 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0003t0008g0052 |
3 | HG02258.hp1 HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.581-670C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | chr8 | 95046324 | |||||||
| chr8:95046457 | T | C | 2 | a0001c0001t0004g0046 a0001c0001t0004g0047 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.581-537T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | chr8 | 95046457 | |||||||
| chr8:95046814 | G | C | 8 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0073 others(5): Show |
8 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.581-180G>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | chr8 | 95046814 | |||||||
| chr8:95046882 | A | G | 2 | a0001c0001t0001g0038 a0001c0001t0001g0177 |
3 | HG02109.hp2 HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.581-112A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | chr8 | 95046882 | |||||||
| chr8:95046990 | A | T | 12 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0062 others(9): Show |
12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
splice_region_variant&intron_variant | LOW | c.581-4A>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 5/8 | chr8 | 95046990 | |||||||
| chr8:95047420 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.714+293C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/8 | chr8 | 95047420 | |||||||
| chr8:95047438 | CTTTAT | C | 4 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0003t0008g0052 others(1): Show |
4 | HG01261.hp1 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.714+323_714+327del others(5): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr8 | 95047438 | ||||||
| chr8:95047507 | T | C | 1 | a0001c0001t0003g0126 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.714+380T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/8 | chr8 | 95047507 | |||||||
| chr8:95047508 | C | CT | 8 | a0001c0001t0001g0009 a0001c0001t0001g0037 a0001c0001t0001g0060 others(5): Show |
13 | HG01109.hp1 HG01358.hp2 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.714+400dupT | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr8 | 95047508 | ||||||
| chr8:95047508 | CTT | C | 12 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0062 others(9): Show |
12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.714+399_714+400del others(2): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr8 | 95047508 | ||||||
| chr8:95047627 | G | A | 12 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0062 others(9): Show |
12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.714+500G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/8 | chr8 | 95047627 | |||||||
| chr8:95047652 | G | A | 1 | a0001c0006t0004g0070 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.714+525G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/8 | chr8 | 95047652 | |||||||
| chr8:95047659 | G | A | 3 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0003t0008g0052 |
3 | HG02258.hp1 HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.714+532G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/8 | chr8 | 95047659 | |||||||
| chr8:95047685 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.714+558A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/8 | chr8 | 95047685 | |||||||
| chr8:95047712 | T | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0027 |
5 | HG02055.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.714+585T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/8 | chr8 | 95047712 | |||||||
| chr8:95047744 | C | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0176 |
3 | HG02145.hp1 HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.714+617C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/8 | chr8 | 95047744 | |||||||
| chr8:95047805 | G | A | 1 | a0001c0001t0001g0030 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.715-652G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/8 | chr8 | 95047805 | |||||||
| chr8:95047807 | C | G | 21 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0021 others(18): Show |
29 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.715-650C>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/8 | chr8 | 95047807 | |||||||
| chr8:95047989 | G | A | 1 | a0001c0001t0001g0032 | 2 | HG02698.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.715-468G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/8 | chr8 | 95047989 | |||||||
| chr8:95048046 | T | C | 2 | a0001c0001t0001g0038 a0001c0001t0001g0177 |
3 | HG02109.hp2 HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.715-411T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/8 | chr8 | 95048046 | |||||||
| chr8:95048078 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.715-379C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/8 | chr8 | 95048078 | |||||||
| chr8:95048143 | A | G | 5 | a0001c0001t0004g0073 a0001c0001t0004g0074 a0001c0002t0005g0075 others(2): Show |
5 | HG02257.hp1 HG02976.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.715-314A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/8 | chr8 | 95048143 | |||||||
| chr8:95048252 | T | C | 12 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0062 others(9): Show |
12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.715-205T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/8 | chr8 | 95048252 | |||||||
| chr8:95048284 | G | A | 8 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0073 others(5): Show |
8 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.715-173G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/8 | chr8 | 95048284 | |||||||
| chr8:95048314 | G | A | 1 | a0001c0001t0001g0033 | 2 | HG01943.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.715-143G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/8 | chr8 | 95048314 | |||||||
| chr8:95048334 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.715-123G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 6/8 | chr8 | 95048334 | |||||||
| chr8:95048839 | A | C | 1 | a0001c0001t0004g0063 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.816+281A>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95048839 | |||||||
| chr8:95048842 | GTGTCTTT others(5): Show |
G | 1 | a0001c0005t0001g0141 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.816+286_816+297del others(12): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr8 | 95048842 | ||||||
| chr8:95048864 | T | C | 12 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0062 others(9): Show |
12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.816+306T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95048864 | |||||||
| chr8:95048887 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.816+329G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95048887 | |||||||
| chr8:95049030 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.816+472A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95049030 | |||||||
| chr8:95049049 | G | A | 12 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0062 others(9): Show |
12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.816+491G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95049049 | |||||||
| chr8:95049124 | C | A | 1 | a0001c0001t0001g0205 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.816+566C>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95049124 | |||||||
| chr8:95049148 | C | T | 1 | a0001c0001t0002g0129 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.816+590C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95049148 | |||||||
| chr8:95049149 | G | A | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.816+591G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95049149 | |||||||
| chr8:95049195 | C | G | 8 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0073 others(5): Show |
8 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.816+637C>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95049195 | |||||||
| chr8:95049209 | CTCT | C | 6 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0092 others(3): Show |
6 | NA18982.hp2 NA18986.hp2 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.816+659_816+661del others(3): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr8 | 95049209 | ||||||
| chr8:95049239 | C | CTT | 12 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0062 others(9): Show |
12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.816+682_816+683ins others(2): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr8 | 95049239 | ||||||
| chr8:95049335 | C | T | 6 | a0001c0001t0003g0012 a0001c0001t0003g0122 a0001c0001t0003g0123 others(3): Show |
9 | HG02145.hp2 HG02257.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.816+777C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95049335 | |||||||
| chr8:95049343 | G | T | 1 | a0001c0001t0004g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.816+785G>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95049343 | |||||||
| chr8:95049391 | A | T | 12 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0062 others(9): Show |
12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.816+833A>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95049391 | |||||||
| chr8:95049472 | A | G | 12 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0062 others(9): Show |
12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.816+914A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95049472 | |||||||
| chr8:95049551 | T | G | 2 | a0001c0001t0001g0103 a0001c0001t0001g0112 |
2 | NA19064.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.816+993T>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95049551 | |||||||
| chr8:95049732 | G | C | 8 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0073 others(5): Show |
8 | HG02257.hp1 HG02258.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.816+1174G>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95049732 | |||||||
| chr8:95049760 | A | G | 1 | a0001c0002t0005g0076 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.816+1202A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95049760 | |||||||
| chr8:95049832 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.816+1274C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95049832 | |||||||
| chr8:95050139 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.816+1581G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95050139 | |||||||
| chr8:95050306 | G | C | 1 | a0001c0001t0001g0025 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.816+1748G>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95050306 | |||||||
| chr8:95050352 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.816+1794G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95050352 | |||||||
| chr8:95050373 | A | G | 61 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(58): Show |
103 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.817-1801A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95050373 | |||||||
| chr8:95050425 | A | C | 1 | a0001c0001t0001g0175 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.817-1749A>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95050425 | |||||||
| chr8:95050702 | T | C | 32 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0021 others(29): Show |
40 | HG00099.hp2 HG00544.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.817-1472T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95050702 | |||||||
| chr8:95051184 | T | C | 8 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0073 others(5): Show |
8 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.817-990T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95051184 | |||||||
| chr8:95051304 | C | T | 3 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 |
3 | HG01891.hp2 HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.817-870C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95051304 | |||||||
| chr8:95051385 | G | C | 6 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0092 others(3): Show |
6 | NA18982.hp2 NA18986.hp2 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.817-789G>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95051385 | |||||||
| chr8:95051392 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.817-782T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95051392 | |||||||
| chr8:95051479 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.817-695A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95051479 | |||||||
| chr8:95051502 | T | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(191): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.817-672T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95051502 | |||||||
| chr8:95051590 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.817-584C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95051590 | |||||||
| chr8:95051760 | G | A | 9 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0042 others(6): Show |
13 | HG00621.hp1 HG02040.hp1 HG02165.hp1 others(10): Show |
intron_variant | MODIFIER | c.817-414G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95051760 | |||||||
| chr8:95051772 | A | G | 3 | a0001c0001t0002g0129 a0001c0001t0002g0130 a0001c0001t0006g0028 |
4 | HG01884.hp1 HG03041.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.817-402A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95051772 | |||||||
| chr8:95051808 | G | A | 12 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0062 others(9): Show |
12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.817-366G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95051808 | |||||||
| chr8:95051970 | G | C | 2 | a0001c0001t0002g0129 a0001c0001t0002g0130 |
2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.817-204G>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 7/8 | chr8 | 95051970 | |||||||
| chr8:95052327 | C | T | 6 | a0001c0001t0003g0012 a0001c0001t0003g0122 a0001c0001t0003g0123 others(3): Show |
9 | HG02145.hp2 HG02257.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.873+97C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95052327 | |||||||
| chr8:95052424 | G | A | 3 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0003t0008g0052 |
3 | HG02258.hp1 HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.873+194G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95052424 | |||||||
| chr8:95052514 | G | T | 12 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0062 others(9): Show |
12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.873+284G>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95052514 | |||||||
| chr8:95052579 | T | C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0183 a0001c0001t0001g0191 |
5 | HG00642.hp2 HG01074.hp1 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.873+349T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95052579 | |||||||
| chr8:95052629 | T | C | 12 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0062 others(9): Show |
12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.873+399T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95052629 | |||||||
| chr8:95052876 | A | G | 5 | a0001c0001t0004g0073 a0001c0001t0004g0074 a0001c0002t0005g0075 others(2): Show |
5 | HG02257.hp1 HG02976.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.873+646A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95052876 | |||||||
| chr8:95053058 | A | G | 3 | a0001c0001t0002g0129 a0001c0001t0002g0130 a0001c0001t0006g0028 |
4 | HG01884.hp1 HG03041.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.873+828A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95053058 | |||||||
| chr8:95053150 | A | G | 12 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0062 others(9): Show |
12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.873+920A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95053150 | |||||||
| chr8:95053155 | A | T | 12 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0062 others(9): Show |
12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.873+925A>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95053155 | |||||||
| chr8:95053275 | G | A | 3 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0007g0048 |
3 | HG02630.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.873+1045G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95053275 | |||||||
| chr8:95053380 | T | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0100 |
3 | HG00609.hp2 HG00673.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.873+1150T>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95053380 | |||||||
| chr8:95053627 | C | CTTT | 3 | a0001c0002t0005g0075 a0001c0002t0005g0076 a0001c0002t0005g0077 |
3 | HG02257.hp1 HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.873+1398_873+1400d others(5): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr8 | 95053627 | ||||||
| chr8:95053631 | C | T | 11 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0062 others(8): Show |
11 | HG02257.hp1 HG02258.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.873+1401C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95053631 | |||||||
| chr8:95053650 | G | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(51): Show |
104 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.873+1420G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95053650 | |||||||
| chr8:95053746 | C | T | 3 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0007g0048 |
3 | HG02630.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.873+1516C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95053746 | |||||||
| chr8:95053791 | G | A | 12 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0062 others(9): Show |
12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.873+1561G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95053791 | |||||||
| chr8:95053916 | C | T | 8 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0073 others(5): Show |
8 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.873+1686C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95053916 | |||||||
| chr8:95053923 | G | A | 4 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0003t0008g0052 others(1): Show |
4 | HG01261.hp1 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.873+1693G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95053923 | |||||||
| chr8:95053925 | C | CT | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(124): Show |
221 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.873+1722dupT | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr8 | 95053925 | ||||||
| chr8:95053925 | C | CTT | 38 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0019 others(35): Show |
53 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.873+1721_873+1722d others(4): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr8 | 95053925 | ||||||
| chr8:95053952 | T | G | 2 | a0001c0001t0004g0062 a0001c0003t0008g0052 |
2 | HG02258.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.873+1722T>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95053952 | |||||||
| chr8:95054093 | T | C | 12 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0062 others(9): Show |
12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.873+1863T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95054093 | |||||||
| chr8:95054237 | G | A | 1 | a0001c0006t0004g0070 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.873+2007G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95054237 | |||||||
| chr8:95054269 | TG | T | 8 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0073 others(5): Show |
8 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.873+2040delG | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95054269 | |||||||
| chr8:95054355 | G | A | 3 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0007g0048 |
3 | HG02630.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.873+2125G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95054355 | |||||||
| chr8:95054418 | C | G | 1 | a0001c0001t0001g0067 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.873+2188C>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95054418 | |||||||
| chr8:95054436 | CT | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.873+2222delT | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr8 | 95054436 | ||||||
| chr8:95054630 | T | C | 3 | a0001c0001t0002g0121 a0001c0001t0002g0127 a0001c0007t0002g0128 |
3 | HG01109.hp2 HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.873+2400T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95054630 | |||||||
| chr8:95054654 | C | G | 1 | a0001c0001t0001g0116 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.873+2424C>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95054654 | |||||||
| chr8:95054736 | C | G | 1 | a0001c0001t0004g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.873+2506C>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95054736 | |||||||
| chr8:95054818 | C | T | 4 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0003t0008g0052 others(1): Show |
4 | HG01261.hp1 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.873+2588C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95054818 | |||||||
| chr8:95054846 | A | C | 12 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0062 others(9): Show |
12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.873+2616A>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95054846 | |||||||
| chr8:95054908 | A | T | 8 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0073 others(5): Show |
8 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.873+2678A>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95054908 | |||||||
| chr8:95055174 | G | T | 1 | a0001c0001t0001g0199 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.874-2635G>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95055174 | |||||||
| chr8:95055185 | A | G | 4 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0003t0008g0052 others(1): Show |
4 | HG01261.hp1 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.874-2624A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95055185 | |||||||
| chr8:95055530 | A | G | 2 | a0001c0001t0004g0046 a0001c0001t0004g0047 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.874-2279A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95055530 | |||||||
| chr8:95055621 | C | T | 1 | a0001c0001t0001g0035 | 2 | HG00438.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.874-2188C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95055621 | |||||||
| chr8:95055639 | A | G | 3 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0006g0028 |
4 | HG02723.hp1 HG02970.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.874-2170A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95055639 | |||||||
| chr8:95055646 | G | A | 1 | a0001c0001t0001g0174 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.874-2163G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95055646 | |||||||
| chr8:95055660 | G | A | 12 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0062 others(9): Show |
12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.874-2149G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95055660 | |||||||
| chr8:95055709 | A | G | 5 | a0001c0001t0004g0073 a0001c0001t0004g0074 a0001c0002t0005g0075 others(2): Show |
5 | HG02257.hp1 HG02976.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.874-2100A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95055709 | |||||||
| chr8:95055830 | A | G | 1 | a0001c0006t0004g0070 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.874-1979A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95055830 | |||||||
| chr8:95056136 | T | C | 12 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0062 others(9): Show |
12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.874-1673T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95056136 | |||||||
| chr8:95056152 | C | A | 12 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0062 others(9): Show |
12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.874-1657C>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95056152 | |||||||
| chr8:95056195 | C | T | 1 | a0001c0001t0007g0048 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.874-1614C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95056195 | |||||||
| chr8:95056232 | G | GT | 5 | a0001c0001t0001g0043 a0001c0001t0001g0066 a0001c0001t0001g0067 others(2): Show |
6 | HG01891.hp2 HG02723.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.874-1564dupT | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr8 | 95056232 | ||||||
| chr8:95056237 | T | A | 8 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0073 others(5): Show |
8 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.874-1572T>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95056237 | |||||||
| chr8:95056316 | T | A | 1 | a0001c0001t0007g0048 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.874-1493T>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95056316 | |||||||
| chr8:95056356 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.874-1453G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95056356 | |||||||
| chr8:95056389 | T | C | 4 | a0001c0001t0001g0041 a0001c0001t0001g0161 a0001c0001t0001g0198 others(1): Show |
5 | NA18971.hp2 NA18981.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.874-1420T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95056389 | |||||||
| chr8:95056605 | G | C | 1 | a0001c0001t0004g0063 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.874-1204G>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95056605 | |||||||
| chr8:95056632 | T | C | 12 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0062 others(9): Show |
12 | HG01261.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.874-1177T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95056632 | |||||||
| chr8:95056709 | A | G | 2 | a0001c0001t0004g0046 a0001c0001t0004g0047 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.874-1100A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95056709 | |||||||
| chr8:95056743 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.874-1066A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95056743 | |||||||
| chr8:95056837 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.874-972C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95056837 | |||||||
| chr8:95056847 | A | G | 3 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0003t0008g0052 |
3 | HG02258.hp1 HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.874-962A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95056847 | |||||||
| chr8:95056855 | G | A | 3 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0007g0048 |
3 | HG02630.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.874-954G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95056855 | |||||||
| chr8:95056892 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.874-917C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95056892 | |||||||
| chr8:95056905 | C | CA | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.874-890dupA | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr8 | 95056905 | ||||||
| chr8:95056984 | G | C | 1 | a0001c0001t0001g0180 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.874-825G>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95056984 | |||||||
| chr8:95057073 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.874-736C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95057073 | |||||||
| chr8:95057085 | G | A | 2 | a0001c0001t0001g0067 a0001c0001t0001g0068 |
2 | HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.874-724G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95057085 | |||||||
| chr8:95057121 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.874-688C>T | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95057121 | |||||||
| chr8:95057122 | G | A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0177 |
3 | HG02109.hp2 HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.874-687G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95057122 | |||||||
| chr8:95057268 | G | A | 2 | a0001c0001t0004g0046 a0001c0001t0004g0047 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.874-541G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95057268 | |||||||
| chr8:95057326 | T | G | 2 | a0001c0001t0004g0046 a0001c0001t0004g0047 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.874-483T>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95057326 | |||||||
| chr8:95057342 | A | G | 1 | a0001c0001t0001g0173 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.874-467A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95057342 | |||||||
| chr8:95057406 | A | C | 1 | a0001c0001t0001g0173 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.874-403A>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95057406 | |||||||
| chr8:95057449 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.874-360G>A | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95057449 | |||||||
| chr8:95057573 | T | G | 1 | a0001c0001t0001g0201 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.874-236T>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95057573 | |||||||
| chr8:95057601 | A | G | 8 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0073 others(5): Show |
8 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.874-208A>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95057601 | |||||||
| chr8:95057651 | CTTT | C | 3 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0003t0008g0052 |
3 | HG02258.hp1 HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.874-155_874-153del others(3): Show |
NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr8 | 95057651 | ||||||
| chr8:95057699 | C | G | 1 | a0001c0001t0001g0090 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.874-110C>G | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95057699 | |||||||
| chr8:95057739 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.874-70T>C | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | chr8 | 95057739 | |||||||
| chr8:95057745 | G | GT | 19 | a0001c0001t0001g0026 a0001c0001t0001g0078 a0001c0001t0001g0113 others(16): Show |
20 | HG00438.hp1 HG02155.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.874-50dupT | NDUFAF6 | ENSG00000156170.14 | transcript | ENST00000396124.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr8 | 95057745 |