| geneid | 84300 |
|---|---|
| ensemblid | ENSG00000137288.10 |
| hgncid | 21237 |
| symbol | UQCC2 |
| name | ubiquinol-cytochrome c reductase complex assembly factor 2 |
| refseq_nuc | NM_032340.4 |
| refseq_prot | NP_115716.1 |
| ensembl_nuc | ENST00000607484.6 |
| ensembl_prot | ENSP00000476140.1 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 33696764 |
| end | 33711700 |
| strand | - |
| ver | v1.2 |
| region | chr6:33696764-33711700 |
| region5000 | chr6:33691764-33716700 |
| regionname0 | UQCC2_chr6_33696764_33711700 |
| regionname5000 | UQCC2_chr6_33691764_33716700 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 126 | 396 | 93 | 67 | 180 | 14 | 40 | 138 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| a0002 | 0/0 | 126 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| a0003 | 0/0 | 126 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| a0004 | 0/0 | 126 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| a0005 | 0/0 | 126 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 381 | 389 | 87 | 66 | 180 | 14 | 40 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| c0002 | 0/0 | 381 | 5 | 4 | 1 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| c0003 | 0/0 | 381 | 3 | 0 | 3 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| c0004 | 0/0 | 381 | 2 | 2 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| c0005 | 0/0 | 381 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| c0006 | 0/0 | 381 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| c0007 | 0/0 | 381 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 904 | 213 | 10 | 37 | 129 | 5 | 32 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| t0002 | 1/0 | 904 | 119 | 58 | 23 | 26 | 6 | 5 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| t0003 | 0/1 | 904 | 21 | 4 | 5 | 9 | 2 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| t0004 | 0/0 | 904 | 16 | 8 | 1 | 7 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| t0005 | 0/0 | 904 | 8 | 0 | 1 | 4 | 0 | 3 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| t0006 | 0/0 | 905 | 6 | 0 | 0 | 6 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| t0007 | 0/0 | 904 | 6 | 6 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| t0008 | 0/0 | 904 | 6 | 5 | 1 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| t0009 | 0/0 | 904 | 2 | 2 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| t0010 | 0/0 | 904 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| t0011 | 0/0 | 904 | 1 | 0 | 1 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| t0012 | 0/0 | 904 | 1 | 0 | 1 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| t0013 | 0/0 | 904 | 1 | 0 | 0 | 0 | 1 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| t0014 | 0/0 | 904 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 65 | 3 | 19 | 27 | 4 | 12 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0002 | 0/0 | 46 | 2 | 4 | 31 | 1 | 8 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0003 | 0/0 | 21 | 2 | 8 | 7 | 2 | 2 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0004 | 0/0 | 19 | 16 | 0 | 1 | 1 | 1 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0005 | 1/0 | 17 | 13 | 1 | 1 | 0 | 1 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0006 | 0/0 | 16 | 0 | 0 | 16 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0007 | 0/1 | 16 | 2 | 4 | 7 | 2 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0008 | 0/0 | 13 | 0 | 1 | 12 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0009 | 0/0 | 9 | 0 | 1 | 7 | 0 | 1 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0010 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0011 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0012 | 0/0 | 7 | 0 | 1 | 4 | 0 | 2 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0013 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0014 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0015 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0016 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0017 | 0/0 | 5 | 1 | 4 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0018 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0019 | 0/0 | 4 | 2 | 0 | 1 | 1 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0020 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0023 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0024 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0026 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0028 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 381 | 389 | 87 | 66 | 180 | 14 | 40 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| a0001c0002 | 0/0 | 381 | 5 | 4 | 1 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| a0001c0004 | 0/0 | 381 | 2 | 2 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| a0002c0003 | 0/0 | 381 | 3 | 0 | 3 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| a0003c0007 | 0/0 | 381 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| a0004c0006 | 0/0 | 381 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| a0005c0005 | 0/0 | 381 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1284 | 208 | 10 | 34 | 127 | 5 | 32 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| a0001c0001t0002 | 1/0 | 1284 | 112 | 52 | 22 | 26 | 6 | 5 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| a0001c0001t0003 | 0/1 | 1284 | 21 | 4 | 5 | 9 | 2 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| a0001c0001t0004 | 0/0 | 1284 | 15 | 7 | 1 | 7 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| a0001c0001t0005 | 0/0 | 1284 | 8 | 0 | 1 | 4 | 0 | 3 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| a0001c0001t0006 | 0/0 | 1285 | 6 | 0 | 0 | 6 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| a0001c0001t0007 | 0/0 | 1284 | 6 | 6 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| a0001c0001t0008 | 0/0 | 1284 | 6 | 5 | 1 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| a0001c0001t0009 | 0/0 | 1284 | 2 | 2 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| a0001c0001t0010 | 0/0 | 1284 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| a0001c0001t0011 | 0/0 | 1284 | 1 | 0 | 1 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| a0001c0001t0012 | 0/0 | 1284 | 1 | 0 | 1 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| a0001c0001t0013 | 0/0 | 1284 | 1 | 0 | 0 | 0 | 1 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| a0001c0001t0014 | 0/0 | 1284 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| a0001c0002t0002 | 0/0 | 1284 | 5 | 4 | 1 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| a0001c0004t0002 | 0/0 | 1284 | 2 | 2 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| a0002c0003t0001 | 0/0 | 1284 | 3 | 0 | 3 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| a0003c0007t0004 | 0/0 | 1284 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| a0004c0006t0001 | 0/0 | 1284 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| a0005c0005t0001 | 0/0 | 1284 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | copy fasta | chr6 | 33691764 | 33716700 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 65 | 3 | 19 | 27 | 4 | 12 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0002 | 0/0 | 46 | 2 | 4 | 31 | 1 | 8 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0006 | 0/0 | 16 | 0 | 0 | 16 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0009 | 0/0 | 9 | 0 | 1 | 7 | 0 | 1 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0010 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0016 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0017 | 0/0 | 5 | 1 | 4 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0002g0003 | 0/0 | 21 | 2 | 8 | 7 | 2 | 2 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0002g0004 | 0/0 | 19 | 16 | 0 | 1 | 1 | 1 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0002g0005 | 1/0 | 17 | 13 | 1 | 1 | 0 | 1 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0002g0008 | 0/0 | 13 | 0 | 1 | 12 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0002g0011 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0002g0019 | 0/0 | 4 | 2 | 0 | 1 | 1 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0002g0020 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0002g0024 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0002g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0003g0007 | 0/1 | 16 | 2 | 4 | 7 | 2 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0004g0018 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0004g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0004g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0005g0012 | 0/0 | 7 | 0 | 1 | 4 | 0 | 2 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0005g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0006g0014 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0007g0013 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0008g0026 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0008g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0008g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0009g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0010g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0011g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0012g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0013g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0001t0014g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0002t0002g0015 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0004t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0001c0004t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0002c0003t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0002c0003t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0003c0007t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0004c0006t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| a0005c0005t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0019 | EUR | GBR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0007 | EUR | GBR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | GBR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0007 | EUR | GBR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | FIN | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0100 | EUR | FIN | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | CHS | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG00423 | hp1 | a0001 | c0001 | t0004 | g0018 | EAS | CHS | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | CHS | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG00558 | hp1 | a0001 | c0001 | t0006 | g0014 | EAS | CHS | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG00597 | hp1 | a0001 | c0001 | t0005 | g0012 | EAS | CHS | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG00735 | hp2 | a0002 | c0003 | t0001 | g0031 | AMR | PUR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0015 | AMR | PUR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01069 | hp2 | a0001 | c0001 | t0011 | g0101 | AMR | PUR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0090 | AMR | PUR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0086 | AMR | PUR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | PUR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0098 | AMR | CLM | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01255 | hp2 | a0001 | c0001 | t0012 | g0103 | AMR | CLM | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01361 | hp1 | a0001 | c0001 | t0008 | g0026 | AMR | CLM | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | CLM | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01496 | hp2 | a0002 | c0003 | t0001 | g0031 | AMR | CLM | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01515 | hp2 | a0001 | c0001 | t0013 | g0046 | EUR | IBS | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01884 | hp1 | a0001 | c0004 | t0002 | g0112 | AFR | ACB | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0038 | AFR | ACB | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01928 | hp1 | a0002 | c0003 | t0001 | g0066 | AMR | PEL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PEL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PEL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01975 | hp2 | a0001 | c0001 | t0005 | g0012 | AMR | PEL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0094 | AMR | PEL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | KHV | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02055 | hp2 | a0001 | c0002 | t0002 | g0015 | AFR | ACB | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02145 | hp2 | a0001 | c0001 | t0007 | g0013 | AFR | ACB | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CDX | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CDX | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CDX | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | ACB | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0111 | AFR | ACB | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PEL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02280 | hp1 | a0001 | c0004 | t0002 | g0113 | AFR | ACB | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | ACB | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02451 | hp1 | a0001 | c0001 | t0009 | g0034 | AFR | ACB | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0083 | AFR | ACB | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02572 | hp1 | a0003 | c0007 | t0004 | g0074 | AFR | GWD | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02615 | hp2 | a0001 | c0001 | t0008 | g0026 | AFR | GWD | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0085 | AFR | GWD | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0107 | AFR | GWD | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02723 | hp2 | a0001 | c0001 | t0007 | g0013 | AFR | GWD | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02809 | hp1 | a0001 | c0001 | t0007 | g0013 | AFR | GWD | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02818 | hp1 | a0001 | c0001 | t0008 | g0039 | AFR | GWD | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02818 | hp2 | a0001 | c0002 | t0002 | g0015 | AFR | GWD | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0038 | AFR | GWD | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02895 | hp2 | a0001 | c0001 | t0007 | g0013 | AFR | GWD | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02896 | hp1 | a0001 | c0001 | t0007 | g0013 | AFR | GWD | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02897 | hp2 | a0001 | c0001 | t0007 | g0013 | AFR | GWD | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02922 | hp2 | a0001 | c0002 | t0002 | g0015 | AFR | ESN | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ESN | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0109 | AFR | ESN | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0089 | AFR | ESN | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03041 | hp2 | a0001 | c0001 | t0008 | g0026 | AFR | GWD | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03098 | hp1 | a0001 | c0001 | t0008 | g0108 | AFR | MSL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | MSL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03139 | hp1 | a0001 | c0001 | t0009 | g0034 | AFR | ESN | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0105 | AFR | MSL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03225 | hp1 | a0001 | c0001 | t0008 | g0039 | AFR | MSL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | MSL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0077 | AFR | ESN | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0082 | AFR | ESN | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03540 | hp1 | a0001 | c0002 | t0002 | g0015 | AFR | GWD | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | MSL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03688 | hp1 | a0001 | c0001 | t0005 | g0104 | SAS | STU | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03831 | hp2 | a0001 | c0001 | t0005 | g0012 | SAS | BEB | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | STU | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG04184 | hp1 | a0001 | c0001 | t0005 | g0012 | SAS | BEB | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0096 | SAS | STU | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | STU | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | STU | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | YRI | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0087 | AFR | YRI | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHB | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHB | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0080 | AFR | YRI | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0091 | AFR | YRI | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18940 | hp1 | a0001 | c0001 | t0004 | g0106 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18952 | hp2 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18957 | hp1 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18963 | hp2 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18964 | hp2 | a0005 | c0005 | t0001 | g0040 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18969 | hp2 | a0001 | c0001 | t0014 | g0114 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18982 | hp1 | a0001 | c0001 | t0006 | g0014 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18986 | hp1 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18990 | hp2 | a0001 | c0001 | t0006 | g0014 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18998 | hp1 | a0001 | c0001 | t0006 | g0014 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0092 | AFR | LWK | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | LWK | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | LWK | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0041 | AFR | LWK | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19054 | hp2 | a0001 | c0001 | t0006 | g0014 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19063 | hp2 | a0001 | c0001 | t0006 | g0014 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19074 | hp2 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19082 | hp1 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19086 | hp1 | a0004 | c0006 | t0001 | g0054 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | YRI | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | ASW | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ASW | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | TSI | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0024 | EUR | TSI | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | GIH | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0018 | AMR | CLM | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0081 | AFR | ACB | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | ACB | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | ACB | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0110 | AFR | USA | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | USA | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA21309 | hp1 | a0001 | c0001 | t0010 | g0088 | AFR | LWK | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | LWK | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0007 | REF | REF | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0005 | REF | REF | UQCC2_chr6_33691764_33716700 | UQCC2 | chr6 | 33691764 | 33716700 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:33697681
|
T | C | 1 | a0002 | 3 | HG00735.hp2 HG01496.hp2 HG01928.hp1 |
missense_variant | MODERATE | c.353A>G | p.Lys118Arg | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 4/4 | 367/1284 | 353/381 | 118/126 | chr6 | 33697681 | ||
| chr6:33697713
|
C | T | 1 | a0003 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.321G>A | p.Met107Ile | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 4/4 | 335/1284 | 321/381 | 107/126 | chr6 | 33697713 | ||
| chr6:33697726
|
A | G | 1 | a0004 | 1 | NA19086.hp1 | missense_variant | MODERATE | c.308T>C | p.Ile103Thr | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 4/4 | 322/1284 | 308/381 | 103/126 | chr6 | 33697726 | ||
| chr6:33711575
|
C | G | 1 | a0005 | 1 | NA18964.hp2 | missense_variant | MODERATE | c.112G>C | p.Ala38Pro | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/4 | 126/1284 | 112/381 | 38/126 | chr6 | 33711575 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:33700502
|
G | T | 1 | a0001c0004 | 2 | HG01884.hp1 HG02280.hp1 |
synonymous_variant | LOW | c.225C>A | p.Pro75Pro | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 3/4 | 239/1284 | 225/381 | 75/126 | chr6 | 33700502 | ||
| chr6:33711564
|
C | T | 1 | a0001c0002 | 5 | HG00741.hp1 HG02055.hp2 HG02818.hp2 others(2): Show |
synonymous_variant | LOW | c.123G>A | p.Glu41Glu | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/4 | 137/1284 | 123/381 | 41/126 | chr6 | 33711564 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:33696771
|
G | A | 1 | a0001c0001t0006 | 6 | HG00558.hp1 NA18982.hp1 NA18990.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*882C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 4/4 | 882 | chr6 | 33696771 | |||||
| chr6:33696831
|
C | A | 5 | a0001c0001t0004a0001c0001t0006a0001c0001t0008others(2): Show | 29 | HG00423.hp1 HG00558.hp1 HG01069.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*822G>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 4/4 | 822 | chr6 | 33696831 | |||||
| chr6:33696850
|
C | A | 1 | a0001c0001t0012 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*803G>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 4/4 | 803 | chr6 | 33696850 | |||||
| chr6:33696871
|
C | T | 1 | a0001c0001t0005 | 8 | HG00597.hp1 HG01975.hp2 HG03688.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*782G>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 4/4 | 782 | chr6 | 33696871 | |||||
| chr6:33696897
|
C | T | 1 | a0001c0001t0011 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*756G>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 4/4 | 756 | chr6 | 33696897 | |||||
| chr6:33696927
|
G | GT | 1 | a0001c0001t0006 | 6 | HG00558.hp1 NA18982.hp1 NA18990.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*725dupA | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 4/4 | 725 | chr6 | 33696927 | |||||
| chr6:33696953
|
T | C | 13 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(10): Show | 253 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(250): Show |
3_prime_UTR_variant | MODIFIER | c.*700A>G | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 4/4 | 700 | chr6 | 33696953 | |||||
| chr6:33697198
|
G | A | 1 | a0001c0001t0013 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*455C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 4/4 | 455 | chr6 | 33697198 | |||||
| chr6:33697224
|
G | C | 8 | a0001c0001t0001a0001c0001t0005a0001c0001t0012others(5): Show | 224 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(221): Show |
3_prime_UTR_variant | MODIFIER | c.*429C>G | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 4/4 | 429 | chr6 | 33697224 | |||||
| chr6:33697243
|
T | A | 2 | a0001c0001t0003a0001c0001t0007 | 27 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*410A>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 4/4 | 410 | chr6 | 33697243 | |||||
| chr6:33697354
|
C | T | 1 | a0001c0001t0010 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*299G>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 4/4 | 299 | chr6 | 33697354 | |||||
| chr6:33697355
|
G | A | 1 | a0001c0001t0007 | 6 | HG02145.hp2 HG02723.hp2 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*298C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 4/4 | 298 | chr6 | 33697355 | |||||
| chr6:33697541
|
G | A | 1 | a0001c0001t0008 | 6 | HG01361.hp1 HG02615.hp2 HG02818.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*112C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 4/4 | 112 | chr6 | 33697541 | |||||
| chr6:33697637
|
G | A | 1 | a0001c0001t0009 | 2 | HG02451.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*16C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 4/4 | 16 | chr6 | 33697637 | |||||
| chr6:33711690
|
G | A | 1 | a0001c0001t0014 | 1 | NA18969.hp2 | 5_prime_UTR_variant | MODIFIER | c.-4C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/4 | 4 | chr6 | 33711690 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:33697848
|
C | T | 1 | a0001c0001t0004g0107 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.284-98G>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 3/3 | chr6 | 33697848 | ||||||
| chr6:33697877
|
T | C | 2 | a0001c0001t0004g0038a0003c0007t0004g0074 | 3 | HG01891.hp1 HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.284-127A>G | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 3/3 | chr6 | 33697877 | ||||||
| chr6:33697932
|
G | A | 1 | a0001c0001t0008g0039 | 2 | HG02818.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.284-182C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 3/3 | chr6 | 33697932 | ||||||
| chr6:33698100
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.284-350C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 3/3 | chr6 | 33698100 | ||||||
| chr6:33698101
|
C | A | 1 | a0001c0001t0001g0047 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.284-351G>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 3/3 | chr6 | 33698101 | ||||||
| chr6:33698376
|
T | A | 1 | a0001c0002t0002g0015 | 5 | HG00741.hp1 HG02055.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.284-626A>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 3/3 | chr6 | 33698376 | ||||||
| chr6:33698386
|
G | T | 2 | a0001c0004t0002g0112a0001c0004t0002g0113 | 2 | HG01884.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.284-636C>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 3/3 | chr6 | 33698386 | ||||||
| chr6:33698437
|
GA | G | 2 | a0001c0001t0005g0012a0001c0001t0005g0104 | 8 | HG00597.hp1 HG01975.hp2 HG03688.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-688delT | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 3/3 | chr6 | 33698437 | ||||||
| chr6:33698722
|
A | C | 1 | a0001c0001t0004g0107 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.284-972T>G | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 3/3 | chr6 | 33698722 | ||||||
| chr6:33698823
|
C | T | 4 | a0001c0001t0001g0036a0001c0001t0005g0012a0001c0001t0005g0104others(1): Show | 11 | HG00597.hp1 HG01255.hp2 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.284-1073G>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 3/3 | chr6 | 33698823 | ||||||
| chr6:33698838
|
A | G | 1 | a0001c0001t0001g0029 | 2 | NA18944.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.284-1088T>C | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 3/3 | chr6 | 33698838 | ||||||
| chr6:33698929
|
TAA | T | 2 | a0001c0001t0001g0036a0001c0001t0012g0103 | 3 | HG01255.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.284-1181_284-1180d others(4): Show |
UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 3/3 | chr6 | 33698929 | ||||||
| chr6:33698940
|
G | A | 2 | a0001c0001t0001g0048a0001c0002t0002g0015 | 6 | HG00741.hp1 HG02055.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.284-1190C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 3/3 | chr6 | 33698940 | ||||||
| chr6:33698968
|
G | GT | 4 | a0001c0001t0001g0036a0001c0001t0005g0012a0001c0001t0005g0104others(1): Show | 11 | HG00597.hp1 HG01255.hp2 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.284-1219dupA | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 3/3 | chr6 | 33698968 | ||||||
| chr6:33699077
|
T | C | 2 | a0001c0001t0002g0084a0001c0001t0002g0085 | 2 | HG01109.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.284-1327A>G | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 3/3 | chr6 | 33699077 | ||||||
| chr6:33699157
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283+1287G>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 3/3 | chr6 | 33699157 | ||||||
| chr6:33699340
|
C | G | 68 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(65): Show | 242 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(239): Show |
intron_variant | MODIFIER | c.283+1104G>C | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 3/3 | chr6 | 33699340 | ||||||
| chr6:33699422
|
A | G | 58 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(55): Show | 225 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(222): Show |
intron_variant | MODIFIER | c.283+1022T>C | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 3/3 | chr6 | 33699422 | ||||||
| chr6:33699559
|
T | C | 1 | a0001c0001t0002g0077 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.283+885A>G | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 3/3 | chr6 | 33699559 | ||||||
| chr6:33699734
|
A | G | 1 | a0001c0001t0002g0082 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.283+710T>C | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 3/3 | chr6 | 33699734 | ||||||
| chr6:33699828
|
C | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(52): Show | 219 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.283+616G>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 3/3 | chr6 | 33699828 | ||||||
| chr6:33699883
|
C | T | 3 | a0001c0001t0002g0019a0001c0001t0002g0024a0001c0001t0002g0078 | 8 | HG00099.hp1 HG00408.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.283+561G>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 3/3 | chr6 | 33699883 | ||||||
| chr6:33699930
|
C | T | 3 | a0001c0001t0002g0008a0001c0001t0002g0020a0001c0001t0002g0099 | 18 | HG01928.hp2 HG01943.hp2 HG02148.hp1 others(15): Show |
intron_variant | MODIFIER | c.283+514G>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 3/3 | chr6 | 33699930 | ||||||
| chr6:33700004
|
A | T | 6 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0051others(3): Show | 22 | HG00609.hp1 HG00621.hp2 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.283+440T>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 3/3 | chr6 | 33700004 | ||||||
| chr6:33700062
|
A | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(51): Show | 214 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.283+382T>C | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 3/3 | chr6 | 33700062 | ||||||
| chr6:33700080
|
T | C | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(97): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.283+364A>G | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 3/3 | chr6 | 33700080 | ||||||
| chr6:33700188
|
G | T | 82 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(79): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.283+256C>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 3/3 | chr6 | 33700188 | ||||||
| chr6:33700261
|
G | A | 14 | a0001c0001t0004g0018a0001c0001t0004g0037a0001c0001t0004g0038others(11): Show | 28 | HG00423.hp1 HG00558.hp1 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.283+183C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 3/3 | chr6 | 33700261 | ||||||
| chr6:33700328
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.283+116C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 3/3 | chr6 | 33700328 | ||||||
| chr6:33700381
|
T | G | 1 | a0001c0004t0002g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.283+63A>C | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 3/3 | chr6 | 33700381 | ||||||
| chr6:33700561
|
C | A | 2 | a0001c0001t0002g0084a0001c0001t0002g0085 | 2 | HG01109.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.214-48G>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 2/3 | chr6 | 33700561 | ||||||
| chr6:33700593
|
A | G | 60 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(57): Show | 227 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.214-80T>C | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 2/3 | chr6 | 33700593 | ||||||
| chr6:33700641
|
C | T | 1 | a0001c0001t0001g0028 | 2 | HG03942.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.214-128G>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 2/3 | chr6 | 33700641 | ||||||
| chr6:33700650
|
G | A | 1 | a0001c0001t0003g0081 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.214-137C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 2/3 | chr6 | 33700650 | ||||||
| chr6:33700737
|
C | T | 9 | a0001c0001t0002g0004a0001c0001t0002g0087a0001c0001t0002g0089others(6): Show | 28 | HG00280.hp2 HG01070.hp2 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.214-224G>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 2/3 | chr6 | 33700737 | ||||||
| chr6:33700841
|
A | C | 18 | a0001c0001t0001g0057a0001c0001t0002g0011a0001c0001t0002g0019others(15): Show | 49 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(46): Show |
intron_variant | MODIFIER | c.214-328T>G | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 2/3 | chr6 | 33700841 | ||||||
| chr6:33701305
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.213+41G>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 2/3 | chr6 | 33701305 | ||||||
| chr6:33701571
|
T | C | 1 | a0001c0001t0004g0105 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.139-151A>G | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33701571 | ||||||
| chr6:33701663
|
C | T | 1 | a0001c0001t0004g0107 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.139-243G>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33701663 | ||||||
| chr6:33701771
|
G | T | 1 | a0001c0001t0001g0056 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.139-351C>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33701771 | ||||||
| chr6:33701800
|
C | T | 57 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(54): Show | 224 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.139-380G>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33701800 | ||||||
| chr6:33701817
|
C | G | 1 | a0001c0002t0002g0015 | 5 | HG00741.hp1 HG02055.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-397G>C | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33701817 | ||||||
| chr6:33701818
|
G | A | 1 | a0001c0001t0002g0097 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.139-398C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33701818 | ||||||
| chr6:33701833
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.139-413G>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33701833 | ||||||
| chr6:33701878
|
CAGCAGAA others(8): Show |
C | 5 | a0001c0001t0001g0065a0001c0001t0002g0098a0001c0001t0005g0012others(2): Show | 15 | HG00597.hp1 HG00741.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.139-473_139-459del others(15): Show |
UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33701878 | ||||||
| chr6:33701881
|
CA | C | 8 | a0001c0001t0004g0038a0001c0001t0004g0109a0001c0001t0004g0110others(5): Show | 12 | HG01361.hp1 HG01891.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.139-462delT | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33701881 | ||||||
| chr6:33702016
|
G | C | 57 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(54): Show | 224 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.139-596C>G | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33702016 | ||||||
| chr6:33702153
|
T | C | 2 | a0001c0004t0002g0112a0001c0004t0002g0113 | 2 | HG01884.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.139-733A>G | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33702153 | ||||||
| chr6:33702246
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.139-826C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33702246 | ||||||
| chr6:33702251
|
A | G | 57 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(54): Show | 224 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.139-831T>C | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33702251 | ||||||
| chr6:33702327
|
T | C | 1 | a0001c0001t0006g0014 | 6 | HG00558.hp1 NA18982.hp1 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.139-907A>G | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33702327 | ||||||
| chr6:33702336
|
C | CA | 10 | a0001c0001t0001g0030a0001c0001t0004g0038a0001c0001t0004g0107others(7): Show | 15 | HG01069.hp2 HG01361.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.139-917dupT | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33702336 | ||||||
| chr6:33702336
|
C | CAA | 6 | a0001c0001t0004g0018a0001c0001t0004g0037a0001c0001t0004g0105others(3): Show | 16 | HG00423.hp1 HG00558.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.139-918_139-917dup others(2): Show |
UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33702336 | ||||||
| chr6:33702336
|
CA | C | 16 | a0001c0001t0001g0036a0001c0001t0002g0011a0001c0001t0002g0077others(13): Show | 49 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.139-917delT | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33702336 | ||||||
| chr6:33702537
|
T | G | 4 | a0001c0001t0001g0036a0001c0001t0005g0012a0001c0001t0005g0104others(1): Show | 11 | HG00597.hp1 HG01255.hp2 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.139-1117A>C | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33702537 | ||||||
| chr6:33702593
|
G | A | 57 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(54): Show | 224 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.139-1173C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33702593 | ||||||
| chr6:33702629
|
T | C | 57 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(54): Show | 224 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.139-1209A>G | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33702629 | ||||||
| chr6:33702635
|
A | C | 2 | a0001c0001t0002g0082a0001c0001t0002g0083 | 2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.139-1215T>G | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33702635 | ||||||
| chr6:33702705
|
A | G | 29 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0011others(26): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.139-1285T>C | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33702705 | ||||||
| chr6:33702769
|
T | C | 3 | a0001c0001t0004g0109a0001c0001t0004g0110a0001c0001t0004g0111 | 3 | HG02258.hp2 HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.139-1349A>G | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33702769 | ||||||
| chr6:33702950
|
G | A | 1 | a0003c0007t0004g0074 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.139-1530C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33702950 | ||||||
| chr6:33703028
|
G | A | 5 | a0001c0001t0004g0018a0001c0001t0004g0037a0001c0001t0004g0105others(2): Show | 15 | HG00423.hp1 HG00558.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.139-1608C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33703028 | ||||||
| chr6:33703192
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.139-1772C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33703192 | ||||||
| chr6:33703273
|
C | T | 2 | a0001c0001t0002g0084a0001c0001t0002g0085 | 2 | HG01109.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.139-1853G>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33703273 | ||||||
| chr6:33703296
|
T | C | 1 | a0001c0001t0001g0049 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.139-1876A>G | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33703296 | ||||||
| chr6:33703321
|
G | A | 2 | a0001c0001t0002g0011a0001c0001t0011g0101 | 8 | HG01069.hp2 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.139-1901C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33703321 | ||||||
| chr6:33703328
|
TA | T | 53 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(50): Show | 213 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.139-1909delT | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33703328 | ||||||
| chr6:33703384
|
C | T | 1 | a0001c0001t0002g0084 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.139-1964G>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33703384 | ||||||
| chr6:33703429
|
T | C | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(97): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.139-2009A>G | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33703429 | ||||||
| chr6:33703446
|
A | G | 1 | a0001c0001t0002g0096 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.139-2026T>C | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33703446 | ||||||
| chr6:33703479
|
G | A | 14 | a0001c0001t0004g0018a0001c0001t0004g0037a0001c0001t0004g0038others(11): Show | 28 | HG00423.hp1 HG00558.hp1 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.139-2059C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33703479 | ||||||
| chr6:33703492
|
G | A | 1 | a0001c0001t0001g0021 | 3 | NA18946.hp2 NA18949.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.139-2072C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33703492 | ||||||
| chr6:33703632
|
T | C | 1 | a0001c0001t0002g0078 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.139-2212A>G | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33703632 | ||||||
| chr6:33703633
|
TA | T | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(97): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.139-2214delT | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33703633 | ||||||
| chr6:33703635
|
A | T | 1 | a0001c0001t0002g0078 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.139-2215T>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33703635 | ||||||
| chr6:33703869
|
A | G | 14 | a0001c0001t0004g0018a0001c0001t0004g0037a0001c0001t0004g0038others(11): Show | 28 | HG00423.hp1 HG00558.hp1 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.139-2449T>C | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33703869 | ||||||
| chr6:33704055
|
C | A | 1 | a0001c0001t0002g0091 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.139-2635G>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33704055 | ||||||
| chr6:33704080
|
G | T | 15 | a0001c0001t0002g0011a0001c0001t0002g0019a0001c0001t0002g0024others(12): Show | 46 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(43): Show |
intron_variant | MODIFIER | c.139-2660C>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33704080 | ||||||
| chr6:33704270
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.139-2850C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33704270 | ||||||
| chr6:33704282
|
T | C | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(107): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.139-2862A>G | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33704282 | ||||||
| chr6:33704283
|
G | A | 2 | a0001c0001t0002g0094a0001c0001t0004g0107 | 2 | HG01981.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.139-2863C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33704283 | ||||||
| chr6:33704364
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.139-2944T>C | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33704364 | ||||||
| chr6:33704381
|
G | A | 1 | a0001c0001t0004g0107 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.139-2961C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33704381 | ||||||
| chr6:33704393
|
T | G | 3 | a0001c0001t0011g0101a0001c0004t0002g0112a0001c0004t0002g0113 | 3 | HG01069.hp2 HG01884.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.139-2973A>C | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33704393 | ||||||
| chr6:33704449
|
G | A | 17 | a0001c0001t0002g0011a0001c0001t0002g0019a0001c0001t0002g0024others(14): Show | 48 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(45): Show |
intron_variant | MODIFIER | c.139-3029C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33704449 | ||||||
| chr6:33704533
|
T | A | 2 | a0001c0001t0002g0089a0001c0001t0010g0088 | 2 | HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.139-3113A>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33704533 | ||||||
| chr6:33704534
|
C | T | 2 | a0001c0001t0002g0089a0001c0001t0010g0088 | 2 | HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.139-3114G>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33704534 | ||||||
| chr6:33704826
|
T | C | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(98): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.139-3406A>G | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33704826 | ||||||
| chr6:33704970
|
A | G | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(97): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.139-3550T>C | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33704970 | ||||||
| chr6:33705021
|
G | A | 53 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(50): Show | 213 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.139-3601C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33705021 | ||||||
| chr6:33705029
|
ACTT | A | 5 | a0001c0001t0004g0018a0001c0001t0004g0037a0001c0001t0004g0105others(2): Show | 15 | HG00423.hp1 HG00558.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.139-3612_139-3610d others(5): Show |
UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33705029 | ||||||
| chr6:33705033
|
C | CT | 41 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(38): Show | 123 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.139-3614dupA | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33705033 | ||||||
| chr6:33705081
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.139-3661C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33705081 | ||||||
| chr6:33705088
|
C | G | 57 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(54): Show | 224 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.139-3668G>C | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33705088 | ||||||
| chr6:33705107
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.139-3687G>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33705107 | ||||||
| chr6:33705121
|
T | C | 2 | a0001c0001t0002g0084a0001c0001t0002g0085 | 2 | HG01109.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.139-3701A>G | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33705121 | ||||||
| chr6:33705169
|
C | T | 1 | a0001c0001t0002g0035 | 2 | HG02280.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.139-3749G>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33705169 | ||||||
| chr6:33705221
|
T | C | 1 | a0001c0001t0003g0086 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.139-3801A>G | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33705221 | ||||||
| chr6:33705321
|
G | A | 2 | a0001c0004t0002g0112a0001c0004t0002g0113 | 2 | HG01884.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.139-3901C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33705321 | ||||||
| chr6:33705350
|
C | CCT | 57 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(54): Show | 224 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.139-3932_139-3931d others(4): Show |
UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33705350 | ||||||
| chr6:33705446
|
A | T | 5 | a0001c0001t0004g0018a0001c0001t0004g0037a0001c0001t0004g0105others(2): Show | 15 | HG00423.hp1 HG00558.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.139-4026T>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33705446 | ||||||
| chr6:33705490
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.139-4070C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33705490 | ||||||
| chr6:33705589
|
T | C | 13 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0016others(10): Show | 41 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.139-4169A>G | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33705589 | ||||||
| chr6:33705609
|
A | G | 3 | a0001c0001t0001g0027a0001c0001t0001g0069a0004c0006t0001g0054 | 4 | NA18940.hp2 NA18981.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.139-4189T>C | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33705609 | ||||||
| chr6:33706018
|
G | A | 2 | a0001c0001t0002g0093a0001c0001t0002g0094 | 2 | HG01981.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.139-4598C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33706018 | ||||||
| chr6:33706054
|
A | G | 53 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(50): Show | 213 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.139-4634T>C | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33706054 | ||||||
| chr6:33706056
|
A | G | 1 | a0001c0001t0001g0053 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.139-4636T>C | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33706056 | ||||||
| chr6:33706077
|
G | A | 1 | a0001c0004t0002g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.139-4657C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33706077 | ||||||
| chr6:33706136
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.139-4716G>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33706136 | ||||||
| chr6:33706379
|
G | C | 57 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(54): Show | 224 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.139-4959C>G | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33706379 | ||||||
| chr6:33706397
|
C | A | 57 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(54): Show | 224 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.139-4977G>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33706397 | ||||||
| chr6:33706411
|
A | G | 57 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(54): Show | 224 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.139-4991T>C | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33706411 | ||||||
| chr6:33706420
|
G | A | 53 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(50): Show | 213 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.139-5000C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33706420 | ||||||
| chr6:33706421
|
A | G | 53 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(50): Show | 213 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.139-5001T>C | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33706421 | ||||||
| chr6:33706449
|
A | G | 4 | a0001c0001t0001g0036a0001c0001t0005g0012a0001c0001t0005g0104others(1): Show | 11 | HG00597.hp1 HG01255.hp2 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.139-5029T>C | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33706449 | ||||||
| chr6:33706642
|
T | G | 53 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(50): Show | 213 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.138+4907A>C | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33706642 | ||||||
| chr6:33706673
|
G | GGATGAGG others(3): Show |
4 | a0001c0001t0001g0036a0001c0001t0005g0012a0001c0001t0005g0104others(1): Show | 11 | HG00597.hp1 HG01255.hp2 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.138+4866_138+4875d others(12): Show |
UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33706673 | ||||||
| chr6:33706737
|
C | T | 1 | a0001c0001t0001g0051 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.138+4812G>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33706737 | ||||||
| chr6:33706958
|
G | C | 1 | a0001c0001t0001g0064 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.138+4591C>G | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33706958 | ||||||
| chr6:33707352
|
A | C | 1 | a0001c0001t0002g0087 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.138+4197T>G | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33707352 | ||||||
| chr6:33707363
|
G | A | 4 | a0001c0001t0004g0018a0001c0001t0004g0105a0001c0001t0004g0106others(1): Show | 13 | HG00423.hp1 HG00558.hp1 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.138+4186C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33707363 | ||||||
| chr6:33707585
|
C | T | 4 | a0001c0001t0001g0036a0001c0001t0005g0012a0001c0001t0005g0104others(1): Show | 11 | HG00597.hp1 HG01255.hp2 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.138+3964G>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33707585 | ||||||
| chr6:33707637
|
C | T | 5 | a0001c0001t0001g0036a0001c0001t0004g0107a0001c0001t0005g0012others(2): Show | 12 | HG00597.hp1 HG01255.hp2 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.138+3912G>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33707637 | ||||||
| chr6:33707638
|
G | A | 1 | a0001c0001t0008g0108 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.138+3911C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33707638 | ||||||
| chr6:33707658
|
A | G | 1 | a0001c0001t0002g0024 | 3 | HG01361.hp2 HG02257.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.138+3891T>C | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33707658 | ||||||
| chr6:33707669
|
C | T | 1 | a0001c0001t0004g0105 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.138+3880G>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33707669 | ||||||
| chr6:33707812
|
T | G | 1 | a0001c0001t0005g0104 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.138+3737A>C | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33707812 | ||||||
| chr6:33707813
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0065 | 6 | HG00558.hp2 HG00621.hp1 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.138+3736C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33707813 | ||||||
| chr6:33707824
|
G | A | 1 | a0001c0001t0002g0033 | 2 | HG00642.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.138+3725C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33707824 | ||||||
| chr6:33707865
|
A | G | 53 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(50): Show | 213 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.138+3684T>C | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33707865 | ||||||
| chr6:33707956
|
G | A | 1 | a0002c0003t0001g0066 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.138+3593C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33707956 | ||||||
| chr6:33708074
|
A | C | 31 | a0001c0001t0001g0044a0001c0001t0002g0003a0001c0001t0002g0008others(28): Show | 101 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(98): Show |
intron_variant | MODIFIER | c.138+3475T>G | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33708074 | ||||||
| chr6:33708321
|
C | A | 1 | a0001c0001t0011g0101 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.138+3228G>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33708321 | ||||||
| chr6:33708379
|
G | A | 53 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(50): Show | 213 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.138+3170C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33708379 | ||||||
| chr6:33708410
|
A | ATT | 57 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(54): Show | 224 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.138+3138_138+3139i others(4): Show |
UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33708410 | ||||||
| chr6:33708442
|
T | C | 1 | a0001c0001t0002g0033 | 2 | HG00642.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.138+3107A>G | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33708442 | ||||||
| chr6:33708545
|
G | A | 1 | a0001c0001t0001g0022 | 3 | HG02027.hp1 HG02129.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.138+3004C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33708545 | ||||||
| chr6:33708569
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.138+2980G>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33708569 | ||||||
| chr6:33708582
|
G | A | 1 | a0001c0001t0004g0107 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.138+2967C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33708582 | ||||||
| chr6:33708717
|
C | T | 1 | a0001c0001t0004g0109 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.138+2832G>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33708717 | ||||||
| chr6:33708729
|
T | C | 1 | a0001c0001t0002g0092 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.138+2820A>G | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33708729 | ||||||
| chr6:33708779
|
G | A | 7 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0020others(4): Show | 42 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.138+2770C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33708779 | ||||||
| chr6:33708813
|
T | C | 53 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(50): Show | 213 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.138+2736A>G | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33708813 | ||||||
| chr6:33708888
|
G | A | 1 | a0001c0001t0001g0023 | 3 | HG02071.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.138+2661C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33708888 | ||||||
| chr6:33709028
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.138+2521A>G | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33709028 | ||||||
| chr6:33709116
|
A | T | 1 | a0001c0001t0001g0043 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.138+2433T>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33709116 | ||||||
| chr6:33709121
|
G | GAGGTGAA others(4): Show |
1 | a0001c0001t0001g0043 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.138+2427_138+2428i others(13): Show |
UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33709121 | ||||||
| chr6:33709122
|
C | T | 1 | a0001c0001t0001g0043 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.138+2427G>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33709122 | ||||||
| chr6:33709135
|
C | T | 14 | a0001c0001t0004g0018a0001c0001t0004g0037a0001c0001t0004g0038others(11): Show | 28 | HG00423.hp1 HG00558.hp1 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.138+2414G>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33709135 | ||||||
| chr6:33709149
|
C | T | 1 | a0001c0001t0001g0043 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.138+2400G>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33709149 | ||||||
| chr6:33709227
|
C | A | 1 | a0001c0001t0001g0032 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.138+2322G>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33709227 | ||||||
| chr6:33709234
|
TTTCCCAA others(5): Show |
T | 1 | a0001c0001t0001g0043 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.138+2303_138+2314d others(14): Show |
UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33709234 | ||||||
| chr6:33709295
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.138+2254A>G | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33709295 | ||||||
| chr6:33709298
|
T | C | 1 | a0001c0001t0001g0068 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.138+2251A>G | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33709298 | ||||||
| chr6:33709345
|
A | C | 1 | a0001c0001t0003g0095 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.138+2204T>G | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33709345 | ||||||
| chr6:33709356
|
A | C | 1 | a0001c0001t0003g0095 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.138+2193T>G | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33709356 | ||||||
| chr6:33709361
|
T | A | 1 | a0001c0001t0003g0095 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.138+2188A>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33709361 | ||||||
| chr6:33709382
|
T | A | 1 | a0001c0001t0003g0095 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.138+2167A>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33709382 | ||||||
| chr6:33709410
|
T | A | 1 | a0001c0001t0003g0095 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.138+2139A>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33709410 | ||||||
| chr6:33709418
|
T | TTTTCTGG others(85): Show |
1 | a0001c0001t0003g0095 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.138+2130_138+2131i others(94): Show |
UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33709418 | ||||||
| chr6:33709430
|
A | T | 1 | a0001c0001t0003g0095 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.138+2119T>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33709430 | ||||||
| chr6:33709437
|
A | AT | 57 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(54): Show | 224 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.138+2111_138+2112i others(3): Show |
UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33709437 | ||||||
| chr6:33709438
|
G | T | 1 | a0001c0001t0003g0095 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.138+2111C>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33709438 | ||||||
| chr6:33709445
|
A | T | 1 | a0001c0001t0003g0095 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.138+2104T>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33709445 | ||||||
| chr6:33709448
|
C | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(106): Show | 380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.138+2101G>C | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33709448 | ||||||
| chr6:33709458
|
A | G | 57 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(54): Show | 224 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.138+2091T>C | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33709458 | ||||||
| chr6:33709469
|
T | TA | 57 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(54): Show | 224 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.138+2079dupT | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33709469 | ||||||
| chr6:33709499
|
G | A | 4 | a0001c0001t0001g0036a0001c0001t0005g0012a0001c0001t0005g0104others(1): Show | 11 | HG00597.hp1 HG01255.hp2 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.138+2050C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33709499 | ||||||
| chr6:33709545
|
G | C | 2 | a0001c0001t0001g0017a0001c0001t0001g0072 | 6 | HG00733.hp1 HG01074.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.138+2004C>G | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33709545 | ||||||
| chr6:33709623
|
A | G | 57 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(54): Show | 224 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.138+1926T>C | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33709623 | ||||||
| chr6:33709676
|
C | G | 2 | a0001c0001t0002g0098a0001c0002t0002g0015 | 6 | HG00741.hp1 HG01255.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.138+1873G>C | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33709676 | ||||||
| chr6:33709766
|
G | GA | 7 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0002g0020others(4): Show | 14 | HG00741.hp1 HG01255.hp1 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.138+1782dupT | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33709766 | ||||||
| chr6:33709779
|
C | A | 38 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(35): Show | 128 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.138+1770G>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33709779 | ||||||
| chr6:33709793
|
G | T | 3 | a0001c0001t0004g0109a0001c0001t0004g0110a0001c0001t0004g0111 | 3 | HG02258.hp2 HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.138+1756C>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33709793 | ||||||
| chr6:33709799
|
A | G | 1 | a0001c0001t0001g0043 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.138+1750T>C | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33709799 | ||||||
| chr6:33709872
|
G | A | 1 | a0001c0001t0002g0100 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.138+1677C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33709872 | ||||||
| chr6:33709884
|
G | A | 4 | a0001c0001t0001g0017a0001c0001t0001g0070a0001c0001t0001g0071others(1): Show | 8 | HG00733.hp1 HG01074.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.138+1665C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33709884 | ||||||
| chr6:33710017
|
A | G | 1 | a0001c0001t0004g0107 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.138+1532T>C | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33710017 | ||||||
| chr6:33710112
|
T | C | 1 | a0001c0001t0001g0023 | 3 | HG02071.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.138+1437A>G | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33710112 | ||||||
| chr6:33710226
|
C | T | 1 | a0001c0001t0002g0033 | 2 | HG00642.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.138+1323G>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33710226 | ||||||
| chr6:33710227
|
G | A | 14 | a0001c0001t0004g0018a0001c0001t0004g0037a0001c0001t0004g0038others(11): Show | 28 | HG00423.hp1 HG00558.hp1 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.138+1322C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33710227 | ||||||
| chr6:33710249
|
T | A | 1 | a0001c0002t0002g0015 | 5 | HG00741.hp1 HG02055.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.138+1300A>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33710249 | ||||||
| chr6:33710300
|
T | G | 1 | a0001c0001t0001g0073 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.138+1249A>C | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33710300 | ||||||
| chr6:33710346
|
G | A | 1 | a0001c0001t0011g0101 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.138+1203C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33710346 | ||||||
| chr6:33710513
|
C | G | 57 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(54): Show | 224 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.138+1036G>C | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33710513 | ||||||
| chr6:33710545
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.138+1004G>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33710545 | ||||||
| chr6:33710617
|
C | G | 57 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(54): Show | 224 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.138+932G>C | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33710617 | ||||||
| chr6:33710649
|
C | A | 1 | a0001c0001t0002g0102 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.138+900G>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33710649 | ||||||
| chr6:33710651
|
A | G | 5 | a0001c0001t0004g0018a0001c0001t0004g0037a0001c0001t0004g0105others(2): Show | 15 | HG00423.hp1 HG00558.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.138+898T>C | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33710651 | ||||||
| chr6:33710679
|
T | C | 1 | a0001c0001t0001g0075 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.138+870A>G | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33710679 | ||||||
| chr6:33710732
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.138+817A>G | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33710732 | ||||||
| chr6:33711123
|
G | A | 3 | a0001c0001t0004g0109a0001c0001t0004g0110a0001c0001t0004g0111 | 3 | HG02258.hp2 HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.138+426C>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33711123 | ||||||
| chr6:33711284
|
A | G | 58 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(55): Show | 225 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(222): Show |
intron_variant | MODIFIER | c.138+265T>C | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33711284 | ||||||
| chr6:33711289
|
T | C | 4 | a0001c0001t0001g0036a0001c0001t0005g0012a0001c0001t0005g0104others(1): Show | 11 | HG00597.hp1 HG01255.hp2 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.138+260A>G | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33711289 | ||||||
| chr6:33711407
|
G | C | 2 | a0001c0004t0002g0112a0001c0004t0002g0113 | 2 | HG01884.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.138+142C>G | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33711407 | ||||||
| chr6:33711411
|
G | T | 1 | a0001c0002t0002g0015 | 5 | HG00741.hp1 HG02055.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.138+138C>A | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33711411 | ||||||
| chr6:33711452
|
C | A | 1 | a0001c0001t0001g0025 | 3 | NA18939.hp1 NA18942.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.138+97G>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33711452 | ||||||
| chr6:33711462
|
C | A | 13 | a0001c0001t0004g0018a0001c0001t0004g0037a0001c0001t0004g0038others(10): Show | 27 | HG00423.hp1 HG00558.hp1 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.138+87G>T | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33711462 | ||||||
| chr6:33711479
|
G | C | 2 | a0001c0004t0002g0112a0001c0004t0002g0113 | 2 | HG01884.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.138+70C>G | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33711479 | ||||||
| chr6:33711525
|
C | G | 1 | a0001c0001t0003g0041 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.138+24G>C | UQCC2 | ENSG00000137288.10 | transcript | ENST00000607484.6 | protein_coding | 1/3 | chr6 | 33711525 |