Item | Value |
---|---|
geneid | 4704 |
ensemblid | ENSG00000139180.11 |
hgncid | 7693 |
symbol | NDUFA9 |
name | NADH:ubiquinone oxidoreductase subunit A9 |
refseq_nuc | NM_005002.5 |
refseq_prot | NP_004993.1 |
ensembl_nuc | ENST00000266544.10 |
ensembl_prot | ENSP00000266544.5 |
mane_status | MANE Select |
chr | chr12 |
start | 4649114 |
end | 4694317 |
strand | + |
ver | v1.2 |
region | chr12:4649114-4694317 |
region5000 | chr12:4644114-4699317 |
regionname0 | NDUFA9_chr12_4649114_4694317 |
regionname5000 | NDUFA9_chr12_4644114_4699317 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 377 | 349 | 84 | 71 | 144 | 10 | 38 | 118 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | MAAAA others(372): Show |
chr12 | 4644114 | 4699317 |
a0002 | 0/0 | 377 | 4 | 0 | 2 | 0 | 2 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | MAAAA others(372): Show |
chr12 | 4644114 | 4699317 |
a0003 | 0/0 | 377 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | MAAAP others(372): Show |
chr12 | 4644114 | 4699317 |
a0004 | 0/0 | 377 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | MAAAA others(372): Show |
chr12 | 4644114 | 4699317 |
a0005 | 0/0 | 377 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | MAAAA others(372): Show |
chr12 | 4644114 | 4699317 |
a0006 | 0/0 | 377 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | MAAAA others(372): Show |
chr12 | 4644114 | 4699317 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1131 | 347 | 84 | 69 | 144 | 10 | 38 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATGGC others(1126): Show |
chr12 | 4644114 | 4699317 | ||
a0001c0005 | 0/0 | 1131 | 2 | 0 | 2 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATGGC others(1126): Show |
chr12 | 4644114 | 4699317 | ||
a0002c0003 | 0/0 | 1131 | 4 | 0 | 2 | 0 | 2 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATGGC others(1126): Show |
chr12 | 4644114 | 4699317 | ||
a0003c0002 | 0/0 | 1131 | 4 | 4 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATGGC others(1126): Show |
chr12 | 4644114 | 4699317 | ||
a0004c0004 | 0/0 | 1131 | 3 | 3 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATGGC others(1126): Show |
chr12 | 4644114 | 4699317 | ||
a0005c0006 | 0/0 | 1131 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATGGC others(1126): Show |
chr12 | 4644114 | 4699317 | ||
a0006c0007 | 0/0 | 1131 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATGGC others(1126): Show |
chr12 | 4644114 | 4699317 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 8357 | 112 | 14 | 22 | 61 | 2 | 13 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8352): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0002 | 0/0 | 8358 | 86 | 13 | 22 | 41 | 5 | 5 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8353): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0003 | 0/0 | 8357 | 23 | 0 | 6 | 16 | 0 | 1 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8352): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0004 | 0/1 | 8349 | 19 | 5 | 7 | 1 | 1 | 4 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8344): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0005 | 0/0 | 8356 | 18 | 11 | 3 | 1 | 2 | 1 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8351): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0006 | 0/0 | 8357 | 8 | 8 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8352): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0007 | 0/0 | 8356 | 6 | 6 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8351): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0008 | 0/0 | 8358 | 5 | 0 | 0 | 5 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8353): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0010 | 1/0 | 8356 | 3 | 2 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8351): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0011 | 0/0 | 8357 | 3 | 3 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8352): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0012 | 0/0 | 8358 | 3 | 0 | 0 | 0 | 0 | 3 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8353): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0013 | 0/0 | 8357 | 3 | 0 | 1 | 0 | 0 | 2 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8352): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0016 | 0/0 | 8359 | 2 | 0 | 0 | 0 | 0 | 2 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8354): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0017 | 0/0 | 8358 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8353): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0018 | 0/0 | 8356 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8351): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0020 | 0/0 | 8357 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8352): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0021 | 0/0 | 8356 | 2 | 1 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8351): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0022 | 0/0 | 8357 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8352): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0023 | 0/0 | 8349 | 2 | 1 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8344): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0024 | 0/0 | 8350 | 2 | 0 | 0 | 0 | 0 | 2 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8345): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0025 | 0/0 | 8357 | 2 | 0 | 0 | 1 | 0 | 1 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8352): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0026 | 0/0 | 8357 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8352): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0027 | 0/0 | 8358 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8353): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0028 | 0/0 | 8356 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8351): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0029 | 0/0 | 8356 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8351): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0030 | 0/0 | 8358 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8353): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0031 | 0/0 | 8358 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8353): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0032 | 0/0 | 8358 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8353): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0033 | 0/0 | 8358 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8353): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0034 | 0/0 | 8358 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8353): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0035 | 0/0 | 8358 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8353): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0036 | 0/0 | 8356 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8351): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0037 | 0/0 | 8356 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8351): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0038 | 0/0 | 8356 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8351): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0039 | 0/0 | 8356 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8351): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0040 | 0/0 | 8356 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8351): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0041 | 0/0 | 8356 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8351): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0042 | 0/0 | 8357 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8352): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0043 | 0/0 | 8357 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8352): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0044 | 0/0 | 8356 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8351): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0045 | 0/0 | 8357 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8352): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0046 | 0/0 | 8357 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8352): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0047 | 0/0 | 8357 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8352): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0048 | 0/0 | 8357 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8352): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0049 | 0/0 | 11124 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(11119): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0050 | 0/0 | 11124 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(11119): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0051 | 0/0 | 8357 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8352): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0052 | 0/0 | 8357 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8352): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0053 | 0/0 | 8349 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8344): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0054 | 0/0 | 8350 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8345): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0055 | 0/0 | 8349 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8344): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0056 | 0/0 | 8349 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8344): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0057 | 0/0 | 8357 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8352): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0058 | 0/0 | 8356 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8351): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0059 | 0/0 | 8348 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8343): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0063 | 0/0 | 8353 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8348): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0064 | 0/0 | 8357 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8352): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0065 | 0/0 | 8357 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8352): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0066 | 0/0 | 8357 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8352): Show |
chr12 | 4644114 | 4699317 |
a0001c0001t0067 | 0/0 | 8349 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8344): Show |
chr12 | 4644114 | 4699317 |
a0001c0005t0019 | 0/0 | 8356 | 2 | 0 | 2 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8351): Show |
chr12 | 4644114 | 4699317 |
a0002c0003t0009 | 0/0 | 8358 | 4 | 0 | 2 | 0 | 2 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8353): Show |
chr12 | 4644114 | 4699317 |
a0003c0002t0014 | 0/0 | 8356 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8351): Show |
chr12 | 4644114 | 4699317 |
a0003c0002t0015 | 0/0 | 8350 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8345): Show |
chr12 | 4644114 | 4699317 |
a0004c0004t0060 | 0/0 | 8353 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8348): Show |
chr12 | 4644114 | 4699317 |
a0004c0004t0061 | 0/0 | 8353 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8348): Show |
chr12 | 4644114 | 4699317 |
a0004c0004t0062 | 0/0 | 8353 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8348): Show |
chr12 | 4644114 | 4699317 |
a0005c0006t0001 | 0/0 | 8357 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8352): Show |
chr12 | 4644114 | 4699317 |
a0006c0007t0001 | 0/0 | 8357 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | ATTGT others(8352): Show |
chr12 | 4644114 | 4699317 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0003 | 0/0 | 6 | 1 | 5 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0001 | 0/0 | 10 | 1 | 2 | 4 | 1 | 2 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0006 | 0/0 | 4 | 3 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0012 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0023 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0026 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0003g0019 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0003g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0003g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0003g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0003g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0004g0014 | 0/1 | 4 | 0 | 2 | 0 | 1 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0004g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0004g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0004g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0004g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0004g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0004g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0004g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0005g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0005g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0005g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0005g0047 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0005g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0005g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0005g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0005g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0005g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0005g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0005g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0005g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0005g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0006g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0006g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0006g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0006g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0006g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0007g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0007g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0007g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0007g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0007g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0007g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0008g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0008g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0010g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0010g0138 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0010g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0011g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0011g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0012g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0012g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0013g0045 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0013g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0016g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0016g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0017g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0017g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0018g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0018g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0020g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0021g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0021g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0022g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0022g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0023g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0023g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0024g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0024g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0025g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0025g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0026g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0027g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0028g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0029g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0030g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0031g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0032g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0033g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0034g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0035g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0036g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0037g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0038g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0039g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0040g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0041g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0042g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0043g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0044g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0045g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0046g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0047g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0048g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0049g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0050g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0051g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0052g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0053g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0054g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0055g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0056g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0057g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0058g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0059g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0063g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0064g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0065g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0066g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0001t0067g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0001c0005t0019g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0002c0003t0009g0016 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0002c0003t0009g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0003c0002t0014g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0003c0002t0015g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0004c0004t0060g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0004c0004t0061g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0004c0004t0062g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0005c0006t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
a0006c0007t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0002 | g0242 | EUR | GBR | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0230 | EUR | GBR | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0116 | EUR | FIN | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG00438 | hp1 | a0001 | c0001 | t0033 | g0048 | EAS | CHS | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | CHS | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG00544 | hp1 | a0001 | c0001 | t0064 | g0188 | EAS | CHS | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG00558 | hp2 | a0001 | c0001 | t0048 | g0206 | EAS | CHS | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | CHS | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG00639 | hp1 | a0001 | c0001 | t0004 | g0014 | AMR | PUR | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG00642 | hp1 | a0001 | c0001 | t0038 | g0040 | AMR | PUR | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG00733 | hp1 | a0001 | c0001 | t0005 | g0166 | AMR | PUR | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG00733 | hp2 | a0001 | c0001 | t0004 | g0014 | AMR | PUR | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG00735 | hp2 | a0001 | c0001 | t0005 | g0254 | AMR | PUR | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0019 | AMR | PUR | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0198 | AMR | PUR | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01069 | hp1 | a0001 | c0001 | t0004 | g0248 | AMR | PUR | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01070 | hp2 | a0001 | c0001 | t0005 | g0040 | AMR | PUR | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01071 | hp2 | a0001 | c0001 | t0004 | g0249 | AMR | PUR | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01074 | hp1 | a0002 | c0003 | t0009 | g0127 | AMR | PUR | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0180 | AMR | PUR | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0164 | AMR | PUR | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01099 | hp1 | a0001 | c0001 | t0004 | g0091 | AMR | PUR | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0226 | AMR | PUR | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01167 | hp1 | a0001 | c0005 | t0019 | g0030 | AMR | PUR | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01167 | hp2 | a0001 | c0001 | t0065 | g0020 | AMR | PUR | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01168 | hp1 | a0001 | c0001 | t0050 | g0237 | AMR | PUR | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01169 | hp1 | a0001 | c0005 | t0019 | g0030 | AMR | PUR | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01169 | hp2 | a0001 | c0001 | t0049 | g0236 | AMR | PUR | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0170 | AMR | PUR | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01243 | hp2 | a0001 | c0001 | t0004 | g0103 | AMR | PUR | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01255 | hp1 | a0002 | c0003 | t0009 | g0016 | AMR | CLM | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0022 | AMR | CLM | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0177 | AMR | CLM | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01258 | hp2 | a0001 | c0001 | t0013 | g0045 | AMR | CLM | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0227 | AMR | CLM | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | CLM | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0234 | AMR | CLM | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01346 | hp2 | a0001 | c0001 | t0030 | g0125 | AMR | CLM | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0224 | AMR | CLM | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01358 | hp2 | a0001 | c0001 | t0023 | g0152 | AMR | CLM | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | CLM | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01361 | hp2 | a0001 | c0001 | t0004 | g0057 | AMR | CLM | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01433 | hp1 | a0005 | c0006 | t0001 | g0197 | AMR | CLM | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | CLM | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | CLM | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0022 | AMR | CLM | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01515 | hp1 | a0002 | c0003 | t0009 | g0016 | EUR | IBS | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0252 | EUR | IBS | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0179 | EUR | IBS | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01516 | hp2 | a0001 | c0001 | t0005 | g0047 | EUR | IBS | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01517 | hp1 | a0002 | c0003 | t0009 | g0016 | EUR | IBS | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01517 | hp2 | a0001 | c0001 | t0005 | g0047 | EUR | IBS | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01884 | hp1 | a0004 | c0004 | t0062 | g0149 | AFR | ACB | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01884 | hp2 | a0004 | c0004 | t0060 | g0140 | AFR | ACB | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01891 | hp1 | a0001 | c0001 | t0005 | g0146 | AFR | ACB | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01891 | hp2 | a0001 | c0001 | t0063 | g0136 | AFR | ACB | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PEL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01934 | hp1 | a0001 | c0001 | t0067 | g0235 | AMR | PEL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0019 | AMR | PEL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01952 | hp2 | a0001 | c0001 | t0039 | g0162 | AMR | PEL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | KHV | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | KHV | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | KHV | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | KHV | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | KHV | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0184 | EAS | KHV | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | KHV | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02083 | hp1 | a0001 | c0001 | t0025 | g0084 | EAS | KHV | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | KHV | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02129 | hp2 | a0001 | c0001 | t0020 | g0013 | EAS | KHV | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02145 | hp1 | a0001 | c0001 | t0018 | g0054 | AFR | ACB | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02145 | hp2 | a0003 | c0002 | t0014 | g0011 | AFR | ACB | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | CDX | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | CDX | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02257 | hp1 | a0001 | c0001 | t0028 | g0161 | AFR | ACB | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02258 | hp1 | a0001 | c0001 | t0029 | g0079 | AFR | ACB | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02258 | hp2 | a0001 | c0001 | t0006 | g0123 | AFR | ACB | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02280 | hp1 | a0003 | c0002 | t0015 | g0011 | AFR | ACB | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02280 | hp2 | a0001 | c0001 | t0007 | g0070 | AFR | ACB | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02451 | hp1 | a0003 | c0002 | t0014 | g0011 | AFR | ACB | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02451 | hp2 | a0001 | c0001 | t0007 | g0200 | AFR | ACB | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02523 | hp1 | a0001 | c0001 | t0021 | g0115 | EAS | KHV | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | KHV | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02572 | hp1 | a0001 | c0001 | t0054 | g0051 | AFR | GWD | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02622 | hp1 | a0001 | c0001 | t0041 | g0088 | AFR | GWD | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02622 | hp2 | a0001 | c0001 | t0006 | g0122 | AFR | GWD | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02630 | hp1 | a0001 | c0001 | t0007 | g0139 | AFR | GWD | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02647 | hp1 | a0001 | c0001 | t0004 | g0033 | AFR | GWD | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02647 | hp2 | a0001 | c0001 | t0017 | g0154 | AFR | GWD | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02683 | hp1 | a0001 | c0001 | t0004 | g0172 | SAS | PJL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02698 | hp1 | a0001 | c0001 | t0012 | g0130 | SAS | PJL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02717 | hp1 | a0001 | c0001 | t0005 | g0137 | AFR | GWD | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02717 | hp2 | a0001 | c0001 | t0010 | g0141 | AFR | GWD | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02723 | hp1 | a0001 | c0001 | t0011 | g0029 | AFR | GWD | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02735 | hp1 | a0001 | c0001 | t0024 | g0024 | SAS | PJL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02738 | hp1 | a0001 | c0001 | t0004 | g0024 | SAS | PJL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02738 | hp2 | a0001 | c0001 | t0042 | g0238 | SAS | PJL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02809 | hp1 | a0001 | c0001 | t0053 | g0033 | AFR | GWD | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0142 | AFR | GWD | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0155 | AFR | GWD | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0134 | AFR | GWD | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0148 | AFR | GWD | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02895 | hp2 | a0001 | c0001 | t0021 | g0002 | AFR | GWD | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02896 | hp1 | a0001 | c0001 | t0005 | g0192 | AFR | GWD | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02896 | hp2 | a0006 | c0007 | t0001 | g0150 | AFR | GWD | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | GWD | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02897 | hp2 | a0001 | c0001 | t0005 | g0042 | AFR | GWD | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02922 | hp1 | a0001 | c0001 | t0007 | g0080 | AFR | ESN | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02965 | hp1 | a0001 | c0001 | t0037 | g0066 | AFR | ESN | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02965 | hp2 | a0001 | c0001 | t0045 | g0199 | AFR | ESN | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0094 | AFR | ESN | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02976 | hp1 | a0001 | c0001 | t0044 | g0195 | AFR | ESN | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02976 | hp2 | a0001 | c0001 | t0026 | g0050 | AFR | ESN | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG03041 | hp1 | a0001 | c0001 | t0023 | g0153 | AFR | GWD | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG03041 | hp2 | a0001 | c0001 | t0010 | g0128 | AFR | GWD | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG03098 | hp2 | a0001 | c0001 | t0040 | g0163 | AFR | MSL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG03130 | hp1 | a0001 | c0001 | t0004 | g0069 | AFR | ESN | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG03130 | hp2 | a0001 | c0001 | t0066 | g0193 | AFR | ESN | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG03139 | hp1 | a0001 | c0001 | t0005 | g0042 | AFR | ESN | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG03139 | hp2 | a0001 | c0001 | t0005 | g0018 | AFR | ESN | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG03195 | hp1 | a0001 | c0001 | t0005 | g0018 | AFR | ESN | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG03195 | hp2 | a0001 | c0001 | t0026 | g0050 | AFR | ESN | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | MSL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | MSL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0231 | SAS | PJL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG03239 | hp2 | a0001 | c0001 | t0013 | g0212 | SAS | PJL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG03453 | hp1 | a0001 | c0001 | t0006 | g0036 | AFR | MSL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG03453 | hp2 | a0001 | c0001 | t0005 | g0144 | AFR | MSL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG03486 | hp2 | a0001 | c0001 | t0006 | g0151 | AFR | MSL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG03491 | hp1 | a0001 | c0001 | t0035 | g0001 | SAS | PJL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG03491 | hp2 | a0001 | c0001 | t0004 | g0044 | SAS | PJL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG03492 | hp1 | a0001 | c0001 | t0004 | g0044 | SAS | PJL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG03540 | hp1 | a0001 | c0001 | t0017 | g0052 | AFR | GWD | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG03540 | hp2 | a0001 | c0001 | t0005 | g0065 | AFR | GWD | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0087 | AFR | MSL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG03654 | hp1 | a0001 | c0001 | t0016 | g0219 | SAS | PJL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG03654 | hp2 | a0001 | c0001 | t0046 | g0183 | SAS | PJL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG03669 | hp2 | a0001 | c0001 | t0016 | g0058 | SAS | PJL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0232 | SAS | PJL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0215 | SAS | BEB | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG03834 | hp2 | a0001 | c0001 | t0024 | g0131 | SAS | BEB | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG03927 | hp1 | a0001 | c0001 | t0012 | g0010 | SAS | BEB | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG04184 | hp2 | a0001 | c0001 | t0025 | g0002 | SAS | BEB | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0207 | SAS | STU | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG04199 | hp2 | a0001 | c0001 | t0012 | g0010 | SAS | STU | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG04204 | hp1 | a0001 | c0001 | t0013 | g0045 | SAS | STU | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | STU | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG04228 | hp1 | a0001 | c0001 | t0005 | g0124 | SAS | STU | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | STU | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18522 | hp1 | a0001 | c0001 | t0011 | g0029 | AFR | YRI | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18522 | hp2 | a0001 | c0001 | t0006 | g0036 | AFR | YRI | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0145 | AFR | YRI | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18906 | hp2 | a0001 | c0001 | t0006 | g0159 | AFR | YRI | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18944 | hp2 | a0001 | c0001 | t0034 | g0178 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18949 | hp2 | a0001 | c0001 | t0058 | g0059 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18961 | hp2 | a0001 | c0001 | t0022 | g0005 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18962 | hp2 | a0001 | c0001 | t0031 | g0006 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18965 | hp1 | a0001 | c0001 | t0005 | g0165 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18968 | hp2 | a0001 | c0001 | t0008 | g0007 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18970 | hp2 | a0001 | c0001 | t0022 | g0004 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18971 | hp1 | a0001 | c0001 | t0057 | g0015 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18972 | hp1 | a0001 | c0001 | t0008 | g0007 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18972 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18979 | hp2 | a0001 | c0001 | t0008 | g0007 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18982 | hp1 | a0001 | c0001 | t0020 | g0013 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18983 | hp1 | a0001 | c0001 | t0008 | g0182 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18983 | hp2 | a0001 | c0001 | t0056 | g0171 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18990 | hp1 | a0001 | c0001 | t0051 | g0025 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19001 | hp2 | a0001 | c0001 | t0032 | g0106 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19005 | hp1 | a0001 | c0001 | t0047 | g0062 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19030 | hp1 | a0001 | c0001 | t0005 | g0055 | AFR | LWK | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19030 | hp2 | a0001 | c0001 | t0007 | g0078 | AFR | LWK | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19043 | hp1 | a0001 | c0001 | t0007 | g0071 | AFR | LWK | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19043 | hp2 | a0001 | c0001 | t0027 | g0089 | AFR | LWK | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19055 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19057 | hp2 | a0001 | c0001 | t0004 | g0102 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19064 | hp2 | a0001 | c0001 | t0055 | g0024 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19072 | hp2 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19078 | hp1 | a0001 | c0001 | t0008 | g0007 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19078 | hp2 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19085 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19086 | hp2 | a0001 | c0001 | t0043 | g0216 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19240 | hp1 | a0001 | c0001 | t0005 | g0018 | AFR | YRI | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | YRI | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA20129 | hp1 | a0001 | c0001 | t0011 | g0076 | AFR | ASW | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA20129 | hp2 | a0004 | c0004 | t0061 | g0251 | AFR | ASW | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA20752 | hp1 | a0001 | c0001 | t0004 | g0014 | EUR | TSI | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0245 | EUR | TSI | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA20905 | hp1 | a0001 | c0001 | t0052 | g0176 | SAS | GIH | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | GIH | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0239 | AMR | CLM | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02109 | hp2 | a0001 | c0001 | t0018 | g0064 | AFR | ACB | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02486 | hp2 | a0001 | c0001 | t0059 | g0194 | AFR | ACB | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG03471 | hp1 | a0001 | c0001 | t0006 | g0034 | AFR | MSL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG06807 | hp1 | a0001 | c0001 | t0006 | g0034 | AFR | USA | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0253 | AFR | USA | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA20300 | hp1 | a0003 | c0002 | t0015 | g0011 | AFR | USA | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | USA | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA21309 | hp1 | a0001 | c0001 | t0036 | g0072 | AFR | LWK | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0191 | AFR | LWK | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0014 | REF | REF | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
homoSapiens | grch38p0 | a0001 | c0001 | t0010 | g0138 | REF | REF | NDUFA9_chr12_4644114_4699317 | NDUFA9 | chr12 | 4644114 | 4699317 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:4649139 | G | C | 1 | a0003 | 4 | HG02145.hp2 HG02280.hp1 HG02451.hp1 others(1): Show |
missense_variant | MODERATE | c.13G>C | p.Ala5Pro | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/11 | 26/8356 | 13/1134 | 5/377 | chr12 | 4649139 | |||
chr12:4654300 | A | G | 1 | a0006 | 1 | HG02896.hp2 | missense_variant | MODERATE | c.58A>G | p.Ile20Val | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 2/11 | 71/8356 | 58/1134 | 20/377 | chr12 | 4654300 | |||
chr12:4654828 | G | A | 1 | a0005 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.224G>A | p.Arg75His | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/11 | 237/8356 | 224/1134 | 75/377 | chr12 | 4654828 | |||
chr12:4654830 | A | C | 1 | a0005 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.226A>C | p.Met76Leu | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/11 | 239/8356 | 226/1134 | 76/377 | chr12 | 4654830 | |||
chr12:4654831 | T | A | 1 | a0005 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.227T>A | p.Met76Lys | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/11 | 240/8356 | 227/1134 | 76/377 | chr12 | 4654831 | |||
chr12:4654832 | G | A | 1 | a0005 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.228G>A | p.Met76Ile | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/11 | 241/8356 | 228/1134 | 76/377 | chr12 | 4654832 | |||
chr12:4654833 | G | T | 1 | a0005 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.229G>T | p.Gly77Trp | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/11 | 242/8356 | 229/1134 | 77/377 | chr12 | 4654833 | |||
chr12:4654863 | G | A | 1 | a0005 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.259G>A | p.Asp87Asn | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/11 | 272/8356 | 259/1134 | 87/377 | chr12 | 4654863 | |||
chr12:4654878 | A | C | 1 | a0005 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.274A>C | p.Met92Leu | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/11 | 287/8356 | 274/1134 | 92/377 | chr12 | 4654878 | |||
chr12:4654880 | G | T | 1 | a0005 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.276G>T | p.Met92Ile | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/11 | 289/8356 | 276/1134 | 92/377 | chr12 | 4654880 | |||
chr12:4654881 | C | T | 1 | a0005 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.277C>T | p.His93Tyr | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/11 | 290/8356 | 277/1134 | 93/377 | chr12 | 4654881 | |||
chr12:4654882 | A | C | 1 | a0005 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.278A>C | p.His93Pro | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/11 | 291/8356 | 278/1134 | 93/377 | chr12 | 4654882 | |||
chr12:4654887 | C | T | 1 | a0005 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.283C>T | p.Arg95Cys | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/11 | 296/8356 | 283/1134 | 95/377 | chr12 | 4654887 | |||
chr12:4654888 | G | A | 1 | a0005 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.284G>A | p.Arg95His | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/11 | 297/8356 | 284/1134 | 95/377 | chr12 | 4654888 | |||
chr12:4654890 | C | A | 1 | a0005 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.286C>A | p.Pro96Thr | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/11 | 299/8356 | 286/1134 | 96/377 | chr12 | 4654890 | |||
chr12:4654899 | G | C | 1 | a0005 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.295G>C | p.Asp99His | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/11 | 308/8356 | 295/1134 | 99/377 | chr12 | 4654899 | |||
chr12:4654905 | G | T | 1 | a0005 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.301G>T | p.Gly101Cys | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/11 | 314/8356 | 301/1134 | 101/377 | chr12 | 4654905 | |||
chr12:4654906 | G | C | 1 | a0005 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.302G>C | p.Gly101Ala | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/11 | 315/8356 | 302/1134 | 101/377 | chr12 | 4654906 | |||
chr12:4654910 | G | T | 1 | a0005 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.306G>T | p.Gln102His | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/11 | 319/8356 | 306/1134 | 102/377 | chr12 | 4654910 | |||
chr12:4682285 | C | T | 1 | a0002 | 4 | HG01074.hp1 HG01255.hp1 HG01515.hp1 others(1): Show |
missense_variant | MODERATE | c.881C>T | p.Pro294Leu | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 9/11 | 894/8356 | 881/1134 | 294/377 | chr12 | 4682285 | |||
chr12:4687105 | T | G | 1 | a0004 | 3 | HG01884.hp1 HG01884.hp2 NA20129.hp2 |
missense_variant | MODERATE | c.1131T>G | p.Ile377Met | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 1144/8356 | 1131/1134 | 377/377 | chr12 | 4687105 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:4654826 | A | T | 1 | a0005c0006 | 1 | HG01433.hp1 | splice_region_variant&synonymous_variant | LOW | c.222A>T | p.Gly74Gly | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/11 | 235/8356 | 222/1134 | 74/377 | chr12 | 4654826 | |||
chr12:4654835 | G | C | 1 | a0005c0006 | 1 | HG01433.hp1 | synonymous_variant | LOW | c.231G>C | p.Gly77Gly | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/11 | 244/8356 | 231/1134 | 77/377 | chr12 | 4654835 | |||
chr12:4654859 | G | C | 1 | a0005c0006 | 1 | HG01433.hp1 | synonymous_variant | LOW | c.255G>C | p.Arg85Arg | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/11 | 268/8356 | 255/1134 | 85/377 | chr12 | 4654859 | |||
chr12:4654865 | T | C | 1 | a0005c0006 | 1 | HG01433.hp1 | synonymous_variant | LOW | c.261T>C | p.Asp87Asp | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/11 | 274/8356 | 261/1134 | 87/377 | chr12 | 4654865 | |||
chr12:4654886 | T | C | 1 | a0005c0006 | 1 | HG01433.hp1 | synonymous_variant | LOW | c.282T>C | p.Leu94Leu | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/11 | 295/8356 | 282/1134 | 94/377 | chr12 | 4654886 | |||
chr12:4654898 | T | C | 1 | a0005c0006 | 1 | HG01433.hp1 | synonymous_variant | LOW | c.294T>C | p.Gly98Gly | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/11 | 307/8356 | 294/1134 | 98/377 | chr12 | 4654898 | |||
chr12:4657759 | G | T | 1 | a0001c0005 | 2 | HG01167.hp1 HG01169.hp1 |
synonymous_variant | LOW | c.330G>T | p.Ala110Ala | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 4/11 | 343/8356 | 330/1134 | 110/377 | chr12 | 4657759 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:4687149 | G | A | 1 | a0001c0001t0027 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*41G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 41 | chr12 | 4687149 | ||||||
chr12:4687444 | C | A | 3 | a0001c0001t0006 a0003c0002t0014 a0003c0002t0015 |
12 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*336C>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 336 | chr12 | 4687444 | ||||||
chr12:4687701 | C | G | 1 | a0001c0001t0067 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*593C>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 593 | chr12 | 4687701 | ||||||
chr12:4687731 | A | C | 67 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(64): Show |
357 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(354): Show |
3_prime_UTR_variant | MODIFIER | c.*623A>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 623 | chr12 | 4687731 | ||||||
chr12:4687787 | T | G | 27 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(24): Show |
149 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*679T>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 679 | chr12 | 4687787 | ||||||
chr12:4687802 | G | T | 2 | a0001c0001t0026 a0001c0001t0066 |
3 | HG02976.hp2 HG03130.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*694G>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 694 | chr12 | 4687802 | ||||||
chr12:4687836 | T | A | 67 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(64): Show |
357 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(354): Show |
3_prime_UTR_variant | MODIFIER | c.*728T>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 728 | chr12 | 4687836 | ||||||
chr12:4687926 | A | G | 1 | a0001c0001t0025 | 2 | HG02083.hp1 HG04184.hp2 |
3_prime_UTR_variant | MODIFIER | c.*818A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 818 | chr12 | 4687926 | ||||||
chr12:4688001 | C | T | 24 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(21): Show |
143 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*893C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 893 | chr12 | 4688001 | ||||||
chr12:4688023 | C | T | 4 | a0001c0001t0003 a0001c0001t0013 a0001c0001t0064 others(1): Show |
28 | HG00544.hp1 HG00738.hp2 HG01081.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*915C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 915 | chr12 | 4688023 | ||||||
chr12:4688239 | T | C | 1 | a0001c0001t0030 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1131T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 1131 | chr12 | 4688239 | ||||||
chr12:4688262 | G | A | 1 | a0001c0001t0031 | 1 | NA18962.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1154G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 1154 | chr12 | 4688262 | ||||||
chr12:4688391 | A | G | 2 | a0001c0001t0013 a0001c0001t0065 |
4 | HG01167.hp2 HG01258.hp2 HG03239.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1283A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 1283 | chr12 | 4688391 | ||||||
chr12:4688480 | G | GA | 58 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(55): Show |
348 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(345): Show |
3_prime_UTR_variant | MODIFIER | c.*1389dupA | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 1390 | INFO_REALIGN_3_PRIME | chr12 | 4688480 | |||||
chr12:4688497 | A | G | 5 | a0001c0001t0029 a0001c0001t0063 a0004c0004t0060 others(2): Show |
5 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1389A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 1389 | chr12 | 4688497 | ||||||
chr12:4688678 | T | C | 25 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(22): Show |
146 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*1570T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 1570 | chr12 | 4688678 | ||||||
chr12:4688757 | G | GTA | 15 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0012 others(12): Show |
111 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*1651_*1652dupAT | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 1653 | INFO_REALIGN_3_PRIME | chr12 | 4688757 | |||||
chr12:4688829 | T | A | 1 | a0004c0004t0060 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1721T>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 1721 | chr12 | 4688829 | ||||||
chr12:4689174 | T | G | 1 | a0002c0003t0009 | 4 | HG01074.hp1 HG01255.hp1 HG01515.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2066T>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 2066 | chr12 | 4689174 | ||||||
chr12:4689189 | C | T | 1 | a0001c0001t0057 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2081C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 2081 | chr12 | 4689189 | ||||||
chr12:4689287 | CTTTTATT | C | 10 | a0001c0001t0004 a0001c0001t0023 a0001c0001t0024 others(7): Show |
30 | HG00639.hp1 HG00733.hp2 HG01069.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2198_*2204delATTT others(3): Show |
NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 2198 | INFO_REALIGN_3_PRIME | chr12 | 4689287 | |||||
chr12:4689344 | G | A | 20 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0008 others(17): Show |
135 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*2236G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 2236 | chr12 | 4689344 | ||||||
chr12:4689367 | A | G | 1 | a0001c0001t0035 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2259A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 2259 | chr12 | 4689367 | ||||||
chr12:4689453 | C | T | 1 | a0001c0001t0038 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2345C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 2345 | chr12 | 4689453 | ||||||
chr12:4689454 | G | A | 9 | a0001c0001t0004 a0001c0001t0023 a0001c0001t0024 others(6): Show |
28 | HG00639.hp1 HG00733.hp2 HG01069.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*2346G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 2346 | chr12 | 4689454 | ||||||
chr12:4689575 | T | G | 9 | a0001c0001t0004 a0001c0001t0023 a0001c0001t0024 others(6): Show |
28 | HG00639.hp1 HG00733.hp2 HG01069.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*2467T>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 2467 | chr12 | 4689575 | ||||||
chr12:4689605 | A | G | 16 | a0001c0001t0001 a0001c0001t0016 a0001c0001t0020 others(13): Show |
132 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*2497A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 2497 | chr12 | 4689605 | ||||||
chr12:4689829 | T | G | 1 | a0001c0001t0053 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2721T>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 2721 | chr12 | 4689829 | ||||||
chr12:4689858 | C | T | 2 | a0001c0001t0041 a0001c0005t0019 |
3 | HG01167.hp1 HG01169.hp1 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2750C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 2750 | chr12 | 4689858 | ||||||
chr12:4689884 | A | G | 59 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(56): Show |
316 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(313): Show |
3_prime_UTR_variant | MODIFIER | c.*2776A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 2776 | chr12 | 4689884 | ||||||
chr12:4689900 | C | T | 9 | a0001c0001t0004 a0001c0001t0023 a0001c0001t0024 others(6): Show |
28 | HG00639.hp1 HG00733.hp2 HG01069.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*2792C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 2792 | chr12 | 4689900 | ||||||
chr12:4689922 | G | A | 9 | a0001c0001t0004 a0001c0001t0023 a0001c0001t0024 others(6): Show |
28 | HG00639.hp1 HG00733.hp2 HG01069.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*2814G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 2814 | chr12 | 4689922 | ||||||
chr12:4689937 | A | G | 2 | a0001c0001t0034 a0001c0001t0043 |
2 | NA18944.hp2 NA19086.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2829A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 2829 | chr12 | 4689937 | ||||||
chr12:4689949 | G | C | 1 | a0001c0001t0066 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2841G>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 2841 | chr12 | 4689949 | ||||||
chr12:4689975 | T | G | 2 | a0001c0001t0041 a0001c0005t0019 |
3 | HG01167.hp1 HG01169.hp1 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2867T>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 2867 | chr12 | 4689975 | ||||||
chr12:4690248 | C | T | 1 | a0001c0001t0037 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3140C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 3140 | chr12 | 4690248 | ||||||
chr12:4690342 | C | T | 1 | a0001c0001t0022 | 2 | NA18961.hp2 NA18970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3234C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 3234 | chr12 | 4690342 | ||||||
chr12:4690507 | A | G | 2 | a0001c0001t0041 a0001c0005t0019 |
3 | HG01167.hp1 HG01169.hp1 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3399A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 3399 | chr12 | 4690507 | ||||||
chr12:4690516 | A | C | 2 | a0001c0001t0039 a0001c0001t0040 |
2 | HG01952.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3408A>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 3408 | chr12 | 4690516 | ||||||
chr12:4690579 | C | T | 1 | a0001c0001t0033 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3471C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 3471 | chr12 | 4690579 | ||||||
chr12:4690645 | G | T | 1 | a0001c0001t0032 | 1 | NA19001.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3537G>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 3537 | chr12 | 4690645 | ||||||
chr12:4690806 | G | C | 1 | a0001c0001t0029 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3698G>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 3698 | chr12 | 4690806 | ||||||
chr12:4690945 | A | G | 1 | a0001c0001t0036 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3837A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 3837 | chr12 | 4690945 | ||||||
chr12:4691104 | A | T | 1 | a0001c0001t0052 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3996A>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 3996 | chr12 | 4691104 | ||||||
chr12:4691264 | G | A | 1 | a0001c0001t0047 | 1 | NA19005.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4156G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 4156 | chr12 | 4691264 | ||||||
chr12:4691474 | C | G | 1 | a0001c0001t0064 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4366C>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 4366 | chr12 | 4691474 | ||||||
chr12:4691770 | G | A | 1 | a0001c0001t0008 | 5 | NA18968.hp2 NA18972.hp1 NA18979.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4662G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 4662 | chr12 | 4691770 | ||||||
chr12:4691813 | TG | T | 34 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(31): Show |
173 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*4716delG | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 4716 | INFO_REALIGN_3_PRIME | chr12 | 4691813 | |||||
chr12:4691816 | G | A | 1 | a0001c0001t0054 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4708G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 4708 | chr12 | 4691816 | ||||||
chr12:4691817 | G | C | 1 | a0001c0001t0023 | 2 | HG01358.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4709G>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 4709 | chr12 | 4691817 | ||||||
chr12:4691822 | G | C | 3 | a0004c0004t0060 a0004c0004t0061 a0004c0004t0062 |
3 | HG01884.hp1 HG01884.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4714G>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 4714 | chr12 | 4691822 | ||||||
chr12:4691901 | T | G | 1 | a0001c0001t0048 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4793T>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 4793 | chr12 | 4691901 | ||||||
chr12:4692152 | G | A | 3 | a0001c0001t0026 a0001c0001t0045 a0001c0001t0066 |
4 | HG02965.hp2 HG02976.hp2 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5044G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 5044 | chr12 | 4692152 | ||||||
chr12:4692170 | C | T | 5 | a0001c0001t0007 a0001c0001t0039 a0001c0001t0040 others(2): Show |
11 | HG01167.hp1 HG01169.hp1 HG01952.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5062C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 5062 | chr12 | 4692170 | ||||||
chr12:4692227 | C | T | 17 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0020 others(14): Show |
134 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*5119C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 5119 | chr12 | 4692227 | ||||||
chr12:4692466 | T | G | 19 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0016 others(16): Show |
137 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*5358T>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 5358 | chr12 | 4692466 | ||||||
chr12:4692597 | G | A | 1 | a0001c0001t0012 | 3 | HG02698.hp1 HG03927.hp1 HG04199.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5489G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 5489 | chr12 | 4692597 | ||||||
chr12:4692619 | G | A | 1 | a0001c0001t0041 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5511G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 5511 | chr12 | 4692619 | ||||||
chr12:4692625 | A | G | 9 | a0001c0001t0004 a0001c0001t0023 a0001c0001t0024 others(6): Show |
28 | HG00639.hp1 HG00733.hp2 HG01069.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*5517A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 5517 | chr12 | 4692625 | ||||||
chr12:4692627 | C | G | 1 | a0001c0001t0045 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5519C>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 5519 | chr12 | 4692627 | ||||||
chr12:4692638 | C | G | 1 | a0001c0001t0020 | 2 | HG02129.hp2 NA18982.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5530C>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 5530 | chr12 | 4692638 | ||||||
chr12:4692801 | C | T | 1 | a0001c0001t0040 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5693C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 5693 | chr12 | 4692801 | ||||||
chr12:4692935 | A | G | 1 | a0001c0001t0017 | 2 | HG02647.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5827A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 5827 | chr12 | 4692935 | ||||||
chr12:4692944 | C | G | 1 | a0001c0001t0056 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5836C>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 5836 | chr12 | 4692944 | ||||||
chr12:4692947 | A | G | 61 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(58): Show |
319 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(316): Show |
3_prime_UTR_variant | MODIFIER | c.*5839A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 5839 | chr12 | 4692947 | ||||||
chr12:4693003 | G | A | 1 | a0001c0001t0029 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5895G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 5895 | chr12 | 4693003 | ||||||
chr12:4693154 | A | G | 1 | a0004c0004t0062 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6046A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 6046 | chr12 | 4693154 | ||||||
chr12:4693173 | A | G | 1 | a0001c0001t0051 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6065A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 6065 | chr12 | 4693173 | ||||||
chr12:4693297 | G | GTAATAAT others(2760): Show |
1 | a0001c0001t0049 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6205_*6206insTTTT others(2763): Show |
NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 6206 | INFO_REALIGN_3_PRIME | chr12 | 4693297 | |||||
chr12:4693297 | G | GTAATAAT others(2760): Show |
1 | a0001c0001t0050 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6205_*6206insTTTT others(2763): Show |
NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 6206 | INFO_REALIGN_3_PRIME | chr12 | 4693297 | |||||
chr12:4693406 | C | T | 1 | a0001c0001t0065 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6298C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 6298 | chr12 | 4693406 | ||||||
chr12:4693786 | G | A | 27 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(24): Show |
149 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*6678G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 6678 | chr12 | 4693786 | ||||||
chr12:4693791 | A | G | 1 | a0001c0001t0018 | 2 | HG02109.hp2 HG02145.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6683A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 6683 | chr12 | 4693791 | ||||||
chr12:4693863 | C | T | 5 | a0001c0001t0007 a0001c0001t0039 a0001c0001t0040 others(2): Show |
11 | HG01167.hp1 HG01169.hp1 HG01952.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*6755C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 6755 | chr12 | 4693863 | ||||||
chr12:4693882 | AAAC | A | 4 | a0001c0001t0063 a0004c0004t0060 a0004c0004t0061 others(1): Show |
4 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6777_*6779delCAA | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 6777 | INFO_REALIGN_3_PRIME | chr12 | 4693882 | |||||
chr12:4694107 | A | G | 1 | a0001c0001t0055 | 1 | NA19064.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6999A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 11/11 | 6999 | chr12 | 4694107 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:4649270 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.49+95C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4649270 | |||||||
chr12:4649622 | A | G | 84 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0043 others(81): Show |
117 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.49+447A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4649622 | |||||||
chr12:4650214 | G | A | 115 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(112): Show |
159 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.49+1039G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4650214 | |||||||
chr12:4650258 | C | T | 1 | a0001c0001t0001g0255 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.49+1083C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4650258 | |||||||
chr12:4650389 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.49+1214C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4650389 | |||||||
chr12:4650443 | A | G | 2 | a0001c0001t0044g0195 a0001c0001t0059g0194 |
2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.49+1268A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4650443 | |||||||
chr12:4650511 | C | T | 3 | a0001c0001t0005g0042 a0001c0001t0005g0192 a0001c0001t0066g0193 |
4 | HG02896.hp1 HG02897.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+1336C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4650511 | |||||||
chr12:4650533 | G | A | 1 | a0001c0001t0007g0080 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.49+1358G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4650533 | |||||||
chr12:4650802 | C | A | 6 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0001g0086 others(3): Show |
6 | HG02083.hp1 NA18972.hp2 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+1627C>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4650802 | |||||||
chr12:4650928 | C | T | 3 | a0001c0001t0002g0026 a0001c0001t0004g0248 a0001c0001t0004g0249 |
5 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+1753C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4650928 | |||||||
chr12:4651063 | A | G | 66 | a0001c0001t0001g0035 a0001c0001t0001g0039 a0001c0001t0001g0041 others(63): Show |
80 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.49+1888A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4651063 | |||||||
chr12:4651151 | A | G | 38 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0173 others(35): Show |
47 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.49+1976A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4651151 | |||||||
chr12:4651271 | A | G | 2 | a0001c0001t0044g0195 a0001c0001t0059g0194 |
2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.49+2096A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4651271 | |||||||
chr12:4651278 | A | G | 1 | a0001c0001t0066g0193 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.49+2103A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4651278 | |||||||
chr12:4651364 | C | T | 2 | a0001c0001t0001g0246 a0001c0001t0002g0247 |
2 | NA19005.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.49+2189C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4651364 | |||||||
chr12:4651419 | C | A | 2 | a0001c0001t0044g0195 a0001c0001t0059g0194 |
2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.49+2244C>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4651419 | |||||||
chr12:4651496 | G | T | 4 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0010g0141 others(1): Show |
5 | HG01515.hp2 HG02717.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+2321G>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4651496 | |||||||
chr12:4651559 | A | G | 116 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(113): Show |
160 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.49+2384A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4651559 | |||||||
chr12:4651582 | A | G | 2 | a0001c0001t0044g0195 a0001c0001t0059g0194 |
2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.49+2407A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4651582 | |||||||
chr12:4651624 | G | A | 262 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(259): Show |
346 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(343): Show |
intron_variant | MODIFIER | c.49+2449G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4651624 | |||||||
chr12:4651812 | G | A | 65 | a0001c0001t0001g0035 a0001c0001t0001g0039 a0001c0001t0001g0041 others(62): Show |
78 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.50-2480G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4651812 | |||||||
chr12:4651845 | T | C | 48 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0143 others(45): Show |
60 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.50-2447T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4651845 | |||||||
chr12:4651882 | A | G | 1 | a0001c0001t0002g0191 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.50-2410A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4651882 | |||||||
chr12:4652047 | G | A | 17 | a0001c0001t0001g0035 a0001c0001t0001g0157 a0001c0001t0001g0158 others(14): Show |
18 | HG01192.hp2 HG01358.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.50-2245G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4652047 | |||||||
chr12:4652289 | A | G | 1 | a0001c0001t0002g0245 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.50-2003A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4652289 | |||||||
chr12:4652353 | T | C | 1 | a0001c0001t0002g0164 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.50-1939T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4652353 | |||||||
chr12:4652388 | G | A | 1 | a0001c0001t0054g0051 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.50-1904G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4652388 | |||||||
chr12:4652394 | G | C | 191 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(188): Show |
251 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.50-1898G>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4652394 | |||||||
chr12:4652485 | T | C | 2 | a0001c0001t0044g0195 a0001c0001t0059g0194 |
2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.50-1807T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4652485 | |||||||
chr12:4652541 | C | T | 65 | a0001c0001t0001g0035 a0001c0001t0001g0039 a0001c0001t0001g0041 others(62): Show |
78 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.50-1751C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4652541 | |||||||
chr12:4652922 | A | G | 2 | a0001c0001t0044g0195 a0001c0001t0059g0194 |
2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.50-1370A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4652922 | |||||||
chr12:4652979 | A | C | 2 | a0001c0001t0044g0195 a0001c0001t0059g0194 |
2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.50-1313A>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4652979 | |||||||
chr12:4652996 | G | A | 1 | a0001c0001t0001g0032 | 2 | HG03098.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.50-1296G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4652996 | |||||||
chr12:4653023 | G | A | 1 | a0001c0001t0017g0052 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.50-1269G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4653023 | |||||||
chr12:4653040 | C | T | 1 | a0001c0001t0029g0079 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.50-1252C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4653040 | |||||||
chr12:4653185 | T | G | 71 | a0001c0001t0001g0035 a0001c0001t0001g0039 a0001c0001t0001g0041 others(68): Show |
86 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.50-1107T>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4653185 | |||||||
chr12:4653272 | C | T | 2 | a0001c0001t0044g0195 a0001c0001t0059g0194 |
2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.50-1020C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4653272 | |||||||
chr12:4653288 | G | A | 4 | a0001c0001t0002g0012 a0001c0001t0002g0198 a0001c0001t0003g0022 others(1): Show |
9 | HG00741.hp1 HG01255.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.50-1004G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4653288 | |||||||
chr12:4653357 | T | A | 2 | a0001c0001t0002g0087 a0001c0001t0041g0088 |
2 | HG02622.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.50-935T>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4653357 | |||||||
chr12:4653505 | T | C | 2 | a0001c0001t0044g0195 a0001c0001t0059g0194 |
2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.50-787T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4653505 | |||||||
chr12:4653559 | A | G | 3 | a0001c0001t0006g0036 a0001c0001t0039g0162 a0001c0001t0040g0163 |
4 | HG01952.hp2 HG03098.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-733A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4653559 | |||||||
chr12:4653603 | C | T | 2 | a0001c0001t0044g0195 a0001c0001t0059g0194 |
2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.50-689C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4653603 | |||||||
chr12:4653615 | A | C | 1 | a0001c0001t0001g0086 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.50-677A>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4653615 | |||||||
chr12:4653705 | CT | C | 8 | a0001c0001t0001g0053 a0001c0001t0001g0246 a0001c0001t0002g0007 others(5): Show |
11 | HG02895.hp1 NA18955.hp2 NA18968.hp2 others(8): Show |
intron_variant | MODIFIER | c.50-572delT | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 4653705 | ||||||
chr12:4653886 | G | A | 2 | a0004c0004t0062g0149 a0006c0007t0001g0150 |
2 | HG01884.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.50-406G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4653886 | |||||||
chr12:4653903 | T | C | 68 | a0001c0001t0001g0035 a0001c0001t0001g0039 a0001c0001t0001g0041 others(65): Show |
82 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.50-389T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4653903 | |||||||
chr12:4653991 | A | G | 8 | a0001c0001t0001g0035 a0001c0001t0001g0157 a0001c0001t0001g0158 others(5): Show |
9 | HG01192.hp2 HG02257.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.50-301A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4653991 | |||||||
chr12:4654031 | G | C | 3 | a0001c0001t0005g0042 a0001c0001t0005g0192 a0001c0001t0066g0193 |
4 | HG02896.hp1 HG02897.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-261G>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4654031 | |||||||
chr12:4654042 | A | G | 2 | a0001c0001t0044g0195 a0001c0001t0059g0194 |
2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.50-250A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4654042 | |||||||
chr12:4654183 | C | T | 115 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(112): Show |
159 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.50-109C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4654183 | |||||||
chr12:4654234 | G | C | 67 | a0001c0001t0001g0035 a0001c0001t0001g0039 a0001c0001t0001g0041 others(64): Show |
80 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.50-58G>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4654234 | |||||||
chr12:4654238 | G | C | 6 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0005g0042 others(3): Show |
8 | HG01515.hp2 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.50-54G>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 1/10 | chr12 | 4654238 | |||||||
chr12:4654513 | G | C | 1 | a0005c0006t0001g0197 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.220+51G>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 2/10 | chr12 | 4654513 | |||||||
chr12:4654516 | T | C | 1 | a0005c0006t0001g0197 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.220+54T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 2/10 | chr12 | 4654516 | |||||||
chr12:4654517 | G | A | 1 | a0005c0006t0001g0197 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.220+55G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 2/10 | chr12 | 4654517 | |||||||
chr12:4654519 | T | G | 1 | a0005c0006t0001g0197 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.220+57T>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 2/10 | chr12 | 4654519 | |||||||
chr12:4654520 | G | A | 1 | a0005c0006t0001g0197 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.220+58G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 2/10 | chr12 | 4654520 | |||||||
chr12:4654522 | G | A | 1 | a0005c0006t0001g0197 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.220+60G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 2/10 | chr12 | 4654522 | |||||||
chr12:4654525 | G | A | 1 | a0005c0006t0001g0197 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.220+63G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 2/10 | chr12 | 4654525 | |||||||
chr12:4654528 | T | C | 1 | a0005c0006t0001g0197 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.220+66T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 2/10 | chr12 | 4654528 | |||||||
chr12:4654529 | G | A | 1 | a0005c0006t0001g0197 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.220+67G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 2/10 | chr12 | 4654529 | |||||||
chr12:4654614 | GCA | G | 114 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(111): Show |
158 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.220+156_220+157del others(2): Show |
NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 4654614 | ||||||
chr12:4654626 | T | A | 1 | a0005c0006t0001g0197 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.220+164T>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 2/10 | chr12 | 4654626 | |||||||
chr12:4654627 | C | A | 1 | a0005c0006t0001g0197 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.220+165C>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 2/10 | chr12 | 4654627 | |||||||
chr12:4654632 | A | G | 1 | a0001c0001t0002g0190 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.220+170A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 2/10 | chr12 | 4654632 | |||||||
chr12:4654722 | A | T | 1 | a0005c0006t0001g0197 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.221-103A>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 2/10 | chr12 | 4654722 | |||||||
chr12:4654741 | A | G | 3 | a0001c0001t0006g0036 a0001c0001t0039g0162 a0001c0001t0040g0163 |
4 | HG01952.hp2 HG03098.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.221-84A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 2/10 | chr12 | 4654741 | |||||||
chr12:4654744 | T | C | 1 | a0005c0006t0001g0197 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.221-81T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 2/10 | chr12 | 4654744 | |||||||
chr12:4654748 | T | C | 1 | a0005c0006t0001g0197 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.221-77T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 2/10 | chr12 | 4654748 | |||||||
chr12:4654762 | C | A | 1 | a0005c0006t0001g0197 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.221-63C>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 2/10 | chr12 | 4654762 | |||||||
chr12:4654971 | G | A | 68 | a0001c0001t0001g0035 a0001c0001t0001g0039 a0001c0001t0001g0041 others(65): Show |
82 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.318+49G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/10 | chr12 | 4654971 | |||||||
chr12:4654992 | C | G | 1 | a0001c0001t0007g0078 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.318+70C>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/10 | chr12 | 4654992 | |||||||
chr12:4655029 | C | T | 66 | a0001c0001t0001g0035 a0001c0001t0001g0039 a0001c0001t0001g0041 others(63): Show |
80 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.318+107C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/10 | chr12 | 4655029 | |||||||
chr12:4655033 | G | A | 2 | a0001c0001t0001g0081 a0001c0001t0001g0086 |
2 | NA18982.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.318+111G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/10 | chr12 | 4655033 | |||||||
chr12:4655239 | G | T | 8 | a0001c0001t0001g0035 a0001c0001t0001g0157 a0001c0001t0001g0158 others(5): Show |
9 | HG01192.hp2 HG02257.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.318+317G>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/10 | chr12 | 4655239 | |||||||
chr12:4655727 | C | T | 1 | a0001c0001t0001g0244 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.318+805C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/10 | chr12 | 4655727 | |||||||
chr12:4655966 | G | A | 4 | a0001c0001t0006g0034 a0001c0001t0006g0036 a0001c0001t0039g0162 others(1): Show |
6 | HG01952.hp2 HG03098.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.318+1044G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/10 | chr12 | 4655966 | |||||||
chr12:4656015 | T | C | 1 | a0001c0005t0019g0030 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.318+1093T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/10 | chr12 | 4656015 | |||||||
chr12:4656053 | CT | C | 3 | a0001c0001t0001g0143 a0001c0001t0002g0142 a0001c0001t0007g0080 |
3 | HG02809.hp2 HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.318+1135delT | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 4656053 | ||||||
chr12:4656105 | A | G | 94 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0035 others(91): Show |
129 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.318+1183A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/10 | chr12 | 4656105 | |||||||
chr12:4656317 | C | T | 145 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0035 others(142): Show |
193 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.318+1395C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/10 | chr12 | 4656317 | |||||||
chr12:4656452 | TC | T | 2 | a0001c0001t0011g0029 a0001c0001t0011g0076 |
3 | HG02723.hp1 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.319-1295delC | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/10 | chr12 | 4656452 | |||||||
chr12:4656487 | G | A | 1 | a0001c0001t0018g0054 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.319-1261G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/10 | chr12 | 4656487 | |||||||
chr12:4656496 | C | T | 2 | a0001c0001t0002g0087 a0001c0001t0041g0088 |
2 | HG02622.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.319-1252C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/10 | chr12 | 4656496 | |||||||
chr12:4657285 | C | T | 47 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0143 others(44): Show |
58 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.319-463C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/10 | chr12 | 4657285 | |||||||
chr12:4657530 | A | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0053 a0001c0001t0001g0073 others(2): Show |
8 | NA18942.hp2 NA18984.hp1 NA18997.hp2 others(5): Show |
intron_variant | MODIFIER | c.319-218A>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/10 | chr12 | 4657530 | |||||||
chr12:4657581 | G | A | 1 | a0001c0001t0045g0199 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.319-167G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/10 | chr12 | 4657581 | |||||||
chr12:4657597 | C | T | 50 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0143 others(47): Show |
61 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.319-151C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/10 | chr12 | 4657597 | |||||||
chr12:4657619 | G | A | 1 | a0001c0001t0011g0076 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.319-129G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/10 | chr12 | 4657619 | |||||||
chr12:4657632 | T | C | 250 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(247): Show |
333 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.319-116T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/10 | chr12 | 4657632 | |||||||
chr12:4657677 | G | A | 8 | a0001c0001t0001g0035 a0001c0001t0001g0157 a0001c0001t0001g0158 others(5): Show |
9 | HG01192.hp2 HG02257.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.319-71G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 3/10 | chr12 | 4657677 | |||||||
chr12:4657983 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.410+144C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 4/10 | chr12 | 4657983 | |||||||
chr12:4658121 | T | G | 1 | a0001c0001t0004g0134 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.410+282T>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 4/10 | chr12 | 4658121 | |||||||
chr12:4658330 | A | T | 50 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0143 others(47): Show |
61 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.410+491A>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 4/10 | chr12 | 4658330 | |||||||
chr12:4658400 | A | C | 50 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0143 others(47): Show |
61 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.410+561A>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 4/10 | chr12 | 4658400 | |||||||
chr12:4658432 | CT | C | 50 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0143 others(47): Show |
61 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.410+594delT | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 4/10 | chr12 | 4658432 | |||||||
chr12:4658477 | C | T | 1 | a0001c0001t0003g0085 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.411-559C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 4/10 | chr12 | 4658477 | |||||||
chr12:4658486 | A | C | 50 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0143 others(47): Show |
61 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.411-550A>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 4/10 | chr12 | 4658486 | |||||||
chr12:4658587 | G | A | 1 | a0001c0001t0004g0091 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.411-449G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 4/10 | chr12 | 4658587 | |||||||
chr12:4658699 | C | T | 47 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0143 others(44): Show |
58 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.411-337C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 4/10 | chr12 | 4658699 | |||||||
chr12:4658718 | A | T | 54 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0143 others(51): Show |
67 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.411-318A>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 4/10 | chr12 | 4658718 | |||||||
chr12:4658732 | A | G | 54 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0143 others(51): Show |
67 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.411-304A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 4/10 | chr12 | 4658732 | |||||||
chr12:4658750 | A | T | 1 | a0001c0001t0002g0189 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.411-286A>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 4/10 | chr12 | 4658750 | |||||||
chr12:4658805 | G | A | 1 | a0001c0001t0005g0166 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.411-231G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 4/10 | chr12 | 4658805 | |||||||
chr12:4658817 | T | G | 1 | a0001c0001t0001g0092 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.411-219T>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 4/10 | chr12 | 4658817 | |||||||
chr12:4658929 | T | C | 116 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(113): Show |
161 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.411-107T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 4/10 | chr12 | 4658929 | |||||||
chr12:4658937 | G | A | 262 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(259): Show |
346 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(343): Show |
intron_variant | MODIFIER | c.411-99G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 4/10 | chr12 | 4658937 | |||||||
chr12:4659027 | A | T | 54 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0143 others(51): Show |
67 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.411-9A>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 4/10 | chr12 | 4659027 | |||||||
chr12:4659188 | A | C | 192 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(189): Show |
260 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.552+11A>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4659188 | |||||||
chr12:4659271 | C | T | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
267 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.552+94C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4659271 | |||||||
chr12:4659338 | C | T | 70 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(67): Show |
93 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.552+161C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4659338 | |||||||
chr12:4659345 | A | G | 50 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0143 others(47): Show |
61 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.552+168A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4659345 | |||||||
chr12:4659355 | TTC | T | 50 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0143 others(47): Show |
61 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.552+180_552+181del others(2): Show |
NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 4659355 | ||||||
chr12:4659411 | G | A | 262 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(259): Show |
346 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(343): Show |
intron_variant | MODIFIER | c.552+234G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4659411 | |||||||
chr12:4659421 | A | C | 1 | a0006c0007t0001g0150 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.552+244A>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4659421 | |||||||
chr12:4659453 | A | G | 198 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(195): Show |
268 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.552+276A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4659453 | |||||||
chr12:4659469 | C | G | 8 | a0001c0001t0001g0035 a0001c0001t0001g0157 a0001c0001t0001g0158 others(5): Show |
9 | HG01192.hp2 HG02257.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.552+292C>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4659469 | |||||||
chr12:4659550 | C | T | 50 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0143 others(47): Show |
61 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.552+373C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4659550 | |||||||
chr12:4659634 | A | C | 55 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0143 others(52): Show |
69 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.552+457A>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4659634 | |||||||
chr12:4659802 | C | A | 2 | a0001c0001t0044g0195 a0001c0001t0059g0194 |
2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.552+625C>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4659802 | |||||||
chr12:4659820 | G | A | 2 | a0001c0001t0005g0018 a0001c0001t0005g0144 |
4 | HG03139.hp2 HG03195.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.552+643G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4659820 | |||||||
chr12:4660073 | C | CA | 3 | a0001c0001t0005g0042 a0001c0001t0005g0192 a0001c0001t0066g0193 |
4 | HG02896.hp1 HG02897.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.552+899dupA | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 4660073 | ||||||
chr12:4660113 | G | C | 2 | a0001c0001t0044g0195 a0001c0001t0059g0194 |
2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.552+936G>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4660113 | |||||||
chr12:4660185 | T | C | 2 | a0003c0002t0014g0011 a0003c0002t0015g0011 |
4 | HG02145.hp2 HG02280.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.552+1008T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4660185 | |||||||
chr12:4660236 | G | A | 1 | a0001c0001t0007g0200 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.552+1059G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4660236 | |||||||
chr12:4660261 | T | C | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | NA19006.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.552+1084T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4660261 | |||||||
chr12:4660382 | C | A | 1 | a0001c0005t0019g0030 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.552+1205C>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4660382 | |||||||
chr12:4660411 | A | G | 1 | a0001c0001t0001g0049 | 2 | HG02074.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.552+1234A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4660411 | |||||||
chr12:4660452 | G | A | 2 | a0004c0004t0062g0149 a0006c0007t0001g0150 |
2 | HG01884.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.552+1275G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4660452 | |||||||
chr12:4660550 | G | C | 2 | a0001c0001t0044g0195 a0001c0001t0059g0194 |
2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.552+1373G>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4660550 | |||||||
chr12:4660572 | C | T | 3 | a0001c0001t0005g0042 a0001c0001t0005g0192 a0001c0001t0066g0193 |
4 | HG02896.hp1 HG02897.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.552+1395C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4660572 | |||||||
chr12:4660635 | C | A | 50 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0143 others(47): Show |
62 | HG00438.hp2 HG00642.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.552+1458C>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4660635 | |||||||
chr12:4660692 | T | G | 5 | a0001c0001t0006g0034 a0001c0001t0006g0036 a0001c0001t0010g0141 others(2): Show |
7 | HG01952.hp2 HG02717.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.552+1515T>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4660692 | |||||||
chr12:4660710 | C | A | 53 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0143 others(50): Show |
67 | HG00438.hp2 HG00642.hp1 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.552+1533C>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4660710 | |||||||
chr12:4660731 | G | A | 7 | a0001c0001t0006g0034 a0001c0001t0006g0036 a0001c0001t0010g0141 others(4): Show |
9 | HG01952.hp2 HG02486.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.552+1554G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4660731 | |||||||
chr12:4660784 | T | A | 57 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0143 others(54): Show |
71 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.552+1607T>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4660784 | |||||||
chr12:4661002 | G | GT | 57 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0143 others(54): Show |
71 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.553-1522dupT | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 4661002 | ||||||
chr12:4661034 | T | G | 4 | a0001c0001t0006g0034 a0001c0001t0006g0036 a0001c0001t0039g0162 others(1): Show |
6 | HG01952.hp2 HG03098.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.553-1499T>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4661034 | |||||||
chr12:4661127 | A | G | 57 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0143 others(54): Show |
71 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.553-1406A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4661127 | |||||||
chr12:4661145 | A | G | 2 | a0001c0001t0039g0162 a0001c0001t0040g0163 |
2 | HG01952.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.553-1388A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4661145 | |||||||
chr12:4661172 | A | G | 2 | a0001c0001t0002g0048 a0001c0001t0033g0048 |
2 | HG00438.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.553-1361A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4661172 | |||||||
chr12:4661405 | A | G | 1 | a0001c0001t0002g0243 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.553-1128A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4661405 | |||||||
chr12:4661503 | G | T | 3 | a0001c0001t0001g0241 a0001c0001t0002g0242 a0001c0001t0004g0014 |
5 | HG00140.hp1 HG00639.hp1 HG00733.hp2 others(2): Show |
intron_variant | MODIFIER | c.553-1030G>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4661503 | |||||||
chr12:4661533 | GTTC | G | 5 | a0001c0001t0002g0168 a0001c0001t0003g0037 a0001c0001t0003g0167 others(2): Show |
6 | HG02080.hp1 NA18953.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.553-995_553-993del others(3): Show |
NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 4661533 | ||||||
chr12:4661582 | G | C | 13 | a0001c0001t0001g0043 a0001c0001t0001g0205 a0001c0001t0001g0246 others(10): Show |
19 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(16): Show |
intron_variant | MODIFIER | c.553-951G>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4661582 | |||||||
chr12:4661688 | A | G | 3 | a0001c0001t0005g0042 a0001c0001t0005g0192 a0001c0001t0066g0193 |
4 | HG02896.hp1 HG02897.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.553-845A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4661688 | |||||||
chr12:4661690 | G | T | 71 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(68): Show |
94 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.553-843G>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4661690 | |||||||
chr12:4661692 | G | A | 2 | a0001c0001t0006g0034 a0001c0001t0006g0036 |
4 | HG03453.hp1 HG03471.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.553-841G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4661692 | |||||||
chr12:4661708 | A | ACTAGAGT others(292): Show |
1 | a0001c0001t0003g0169 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.553-814_553-813ins others(299): Show |
NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 4661708 | ||||||
chr12:4661708 | A | ACTAGAGT others(303): Show |
3 | a0001c0001t0002g0164 a0001c0001t0002g0170 a0001c0001t0002g0191 |
3 | HG01081.hp2 HG01192.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.553-814_553-813ins others(310): Show |
NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 4661708 | ||||||
chr12:4661708 | A | ACTAGAGT others(304): Show |
45 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0143 others(42): Show |
57 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.553-814_553-813ins others(311): Show |
NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 4661708 | ||||||
chr12:4661708 | A | ACTAGAGT others(305): Show |
1 | a0001c0001t0002g0181 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.553-814_553-813ins others(312): Show |
NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 4661708 | ||||||
chr12:4661708 | A | ACTAGAGT others(306): Show |
3 | a0001c0001t0006g0034 a0001c0001t0006g0036 a0001c0001t0010g0141 |
5 | HG02717.hp2 HG03453.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.553-814_553-813ins others(313): Show |
NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 4661708 | ||||||
chr12:4661708 | A | ACTAGAGT others(307): Show |
1 | a0001c0001t0039g0162 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.553-814_553-813ins others(314): Show |
NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 4661708 | ||||||
chr12:4661708 | A | ACTAGAGT others(308): Show |
2 | a0001c0001t0044g0195 a0001c0001t0059g0194 |
2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.553-814_553-813ins others(315): Show |
NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 4661708 | ||||||
chr12:4661708 | A | ACTAGAGT others(308): Show |
1 | a0001c0001t0040g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.553-814_553-813ins others(315): Show |
NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 4661708 | ||||||
chr12:4661836 | A | C | 1 | a0001c0001t0001g0028 | 2 | HG02735.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.553-697A>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4661836 | |||||||
chr12:4661875 | G | T | 7 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0004g0069 others(4): Show |
7 | HG02055.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.553-658G>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4661875 | |||||||
chr12:4661933 | C | G | 36 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0015 others(33): Show |
46 | HG00558.hp1 HG00621.hp2 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.553-600C>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4661933 | |||||||
chr12:4661952 | C | G | 1 | a0001c0001t0002g0132 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.553-581C>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4661952 | |||||||
chr12:4662016 | A | C | 1 | a0001c0001t0001g0143 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.553-517A>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4662016 | |||||||
chr12:4662169 | G | A | 1 | a0001c0001t0003g0022 | 3 | HG01255.hp2 HG01361.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.553-364G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4662169 | |||||||
chr12:4662223 | G | A | 1 | a0001c0001t0002g0207 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.553-310G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4662223 | |||||||
chr12:4662265 | A | G | 227 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(224): Show |
304 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.553-268A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4662265 | |||||||
chr12:4662266 | C | T | 1 | a0001c0001t0024g0131 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.553-267C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4662266 | |||||||
chr12:4662290 | G | A | 40 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0093 others(37): Show |
49 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.553-243G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4662290 | |||||||
chr12:4662516 | G | A | 81 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0043 others(78): Show |
117 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.553-17G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 5/10 | chr12 | 4662516 | |||||||
chr12:4662796 | C | T | 1 | a0001c0001t0012g0130 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.655+161C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4662796 | |||||||
chr12:4662853 | T | G | 1 | a0001c0001t0029g0079 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.655+218T>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4662853 | |||||||
chr12:4662863 | A | G | 1 | a0004c0004t0062g0149 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.655+228A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4662863 | |||||||
chr12:4663049 | G | C | 45 | a0001c0001t0001g0005 a0001c0001t0001g0053 a0001c0001t0001g0098 others(42): Show |
59 | HG00438.hp2 HG00621.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.655+414G>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4663049 | |||||||
chr12:4663153 | T | C | 22 | a0001c0001t0001g0196 a0001c0001t0001g0214 a0001c0001t0001g0217 others(19): Show |
24 | HG00639.hp1 HG00733.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.655+518T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4663153 | |||||||
chr12:4663326 | T | G | 1 | a0001c0001t0002g0142 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.655+691T>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4663326 | |||||||
chr12:4663363 | G | GC | 6 | a0001c0001t0002g0148 a0001c0001t0002g0156 a0001c0001t0004g0094 others(3): Show |
6 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.655+733dupC | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 4663363 | ||||||
chr12:4663378 | G | A | 1 | a0001c0001t0002g0187 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.655+743G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4663378 | |||||||
chr12:4663383 | T | C | 96 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(93): Show |
133 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.655+748T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4663383 | |||||||
chr12:4663455 | A | G | 30 | a0001c0001t0001g0129 a0001c0001t0001g0201 a0001c0001t0001g0202 others(27): Show |
41 | HG00544.hp1 HG00738.hp2 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.655+820A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4663455 | |||||||
chr12:4663505 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.655+870C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4663505 | |||||||
chr12:4663516 | A | G | 1 | a0001c0001t0001g0233 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.655+881A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4663516 | |||||||
chr12:4663522 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.655+887C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4663522 | |||||||
chr12:4663543 | G | A | 9 | a0001c0001t0006g0034 a0001c0001t0006g0036 a0001c0001t0006g0122 others(6): Show |
13 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.655+908G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4663543 | |||||||
chr12:4663891 | T | C | 1 | a0001c0001t0002g0240 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.655+1256T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4663891 | |||||||
chr12:4663969 | G | A | 1 | a0004c0004t0060g0140 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.655+1334G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4663969 | |||||||
chr12:4664073 | G | A | 1 | a0001c0001t0005g0137 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.655+1438G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4664073 | |||||||
chr12:4664076 | T | C | 28 | a0001c0001t0002g0215 a0001c0001t0004g0014 a0001c0001t0004g0024 others(25): Show |
31 | HG00639.hp1 HG00733.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.655+1441T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4664076 | |||||||
chr12:4664107 | A | T | 34 | a0001c0001t0004g0014 a0001c0001t0004g0024 a0001c0001t0004g0033 others(31): Show |
38 | HG00639.hp1 HG00733.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.655+1472A>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4664107 | |||||||
chr12:4664139 | G | A | 24 | a0001c0001t0004g0014 a0001c0001t0004g0024 a0001c0001t0004g0033 others(21): Show |
27 | HG00639.hp1 HG00733.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.655+1504G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4664139 | |||||||
chr12:4664144 | G | A | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(233): Show |
309 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(306): Show |
intron_variant | MODIFIER | c.655+1509G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4664144 | |||||||
chr12:4664187 | A | G | 106 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(103): Show |
142 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.655+1552A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4664187 | |||||||
chr12:4664322 | A | C | 2 | a0001c0001t0026g0050 a0001c0001t0066g0193 |
3 | HG02976.hp2 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.655+1687A>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4664322 | |||||||
chr12:4664323 | G | C | 2 | a0001c0001t0026g0050 a0001c0001t0066g0193 |
3 | HG02976.hp2 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.655+1688G>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4664323 | |||||||
chr12:4664619 | C | T | 1 | a0001c0001t0026g0050 | 2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.655+1984C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4664619 | |||||||
chr12:4664964 | A | G | 1 | a0001c0001t0001g0223 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.655+2329A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4664964 | |||||||
chr12:4665071 | T | G | 1 | a0001c0001t0029g0079 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.655+2436T>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4665071 | |||||||
chr12:4665241 | T | C | 17 | a0001c0001t0005g0018 a0001c0001t0005g0040 a0001c0001t0005g0047 others(14): Show |
20 | HG00642.hp1 HG00733.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.655+2606T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4665241 | |||||||
chr12:4665387 | A | T | 8 | a0001c0001t0006g0034 a0001c0001t0006g0036 a0001c0001t0006g0122 others(5): Show |
12 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.655+2752A>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4665387 | |||||||
chr12:4665543 | A | G | 1 | a0001c0001t0004g0172 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.655+2908A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4665543 | |||||||
chr12:4665746 | G | GT | 107 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(104): Show |
143 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.656-2696dupT | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 4665746 | ||||||
chr12:4665746 | G | GTT | 5 | a0001c0001t0002g0245 a0001c0001t0005g0047 a0001c0001t0005g0137 others(2): Show |
6 | HG01516.hp2 HG01517.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.656-2697_656-2696d others(4): Show |
NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 4665746 | ||||||
chr12:4665746 | G | GTTT | 12 | a0001c0001t0005g0018 a0001c0001t0005g0040 a0001c0001t0005g0055 others(9): Show |
14 | HG00642.hp1 HG00733.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.656-2698_656-2696d others(5): Show |
NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 4665746 | ||||||
chr12:4665746 | GT | G | 72 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(69): Show |
101 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.656-2696delT | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 4665746 | ||||||
chr12:4665750 | T | TG | 2 | a0001c0001t0011g0029 a0001c0001t0011g0076 |
3 | HG02723.hp1 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.656-2707_656-2706i others(3): Show |
NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4665750 | |||||||
chr12:4665812 | T | C | 2 | a0001c0001t0041g0088 a0001c0005t0019g0030 |
3 | HG01167.hp1 HG01169.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.656-2645T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4665812 | |||||||
chr12:4665946 | T | G | 1 | a0001c0001t0063g0136 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.656-2511T>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4665946 | |||||||
chr12:4666065 | A | G | 1 | a0001c0001t0005g0144 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.656-2392A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4666065 | |||||||
chr12:4666185 | T | C | 1 | a0001c0001t0003g0184 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.656-2272T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4666185 | |||||||
chr12:4666295 | T | C | 1 | a0001c0001t0005g0124 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.656-2162T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4666295 | |||||||
chr12:4666388 | G | C | 3 | a0001c0001t0026g0050 a0001c0001t0045g0199 a0001c0001t0066g0193 |
4 | HG02965.hp2 HG02976.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.656-2069G>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4666388 | |||||||
chr12:4666389 | A | T | 1 | a0001c0001t0001g0120 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.656-2068A>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4666389 | |||||||
chr12:4666619 | TGAAA | T | 15 | a0001c0001t0004g0014 a0001c0001t0004g0024 a0001c0001t0004g0044 others(12): Show |
18 | HG00639.hp1 HG00733.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.656-1837_656-1834d others(6): Show |
NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4666619 | |||||||
chr12:4666625 | GA | G | 15 | a0001c0001t0004g0014 a0001c0001t0004g0024 a0001c0001t0004g0044 others(12): Show |
18 | HG00639.hp1 HG00733.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.656-1831delA | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4666625 | |||||||
chr12:4666678 | C | A | 1 | a0001c0001t0006g0122 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.656-1779C>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4666678 | |||||||
chr12:4666680 | T | C | 1 | a0001c0001t0030g0125 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.656-1777T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4666680 | |||||||
chr12:4666732 | C | T | 15 | a0001c0001t0005g0018 a0001c0001t0005g0040 a0001c0001t0005g0047 others(12): Show |
18 | HG00642.hp1 HG00733.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.656-1725C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4666732 | |||||||
chr12:4666896 | C | T | 1 | a0001c0001t0002g0097 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.656-1561C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4666896 | |||||||
chr12:4667018 | A | G | 1 | a0001c0001t0002g0107 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.656-1439A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4667018 | |||||||
chr12:4667053 | C | G | 2 | a0001c0001t0004g0248 a0001c0001t0004g0249 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.656-1404C>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4667053 | |||||||
chr12:4667118 | A | C | 3 | a0001c0001t0001g0015 a0001c0001t0001g0063 a0001c0001t0057g0015 |
4 | NA18971.hp1 NA18988.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.656-1339A>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4667118 | |||||||
chr12:4667231 | A | T | 1 | a0001c0001t0001g0119 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.656-1226A>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4667231 | |||||||
chr12:4667278 | C | G | 1 | a0001c0001t0005g0124 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.656-1179C>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4667278 | |||||||
chr12:4667430 | G | T | 1 | a0001c0001t0001g0158 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.656-1027G>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4667430 | |||||||
chr12:4667505 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.656-952T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4667505 | |||||||
chr12:4667512 | CT | C | 128 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(125): Show |
163 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.656-928delT | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 4667512 | ||||||
chr12:4667512 | CTT | C | 7 | a0001c0001t0002g0017 a0001c0001t0002g0090 a0001c0001t0002g0104 others(4): Show |
9 | HG02080.hp2 HG02165.hp2 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.656-929_656-928del others(2): Show |
NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 4667512 | ||||||
chr12:4667515 | T | G | 1 | a0001c0001t0004g0069 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.656-942T>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4667515 | |||||||
chr12:4667517 | T | G | 4 | a0001c0001t0005g0055 a0001c0001t0005g0137 a0001c0001t0018g0054 others(1): Show |
4 | HG02109.hp2 HG02145.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.656-940T>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4667517 | |||||||
chr12:4667541 | G | A | 1 | a0004c0004t0061g0251 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.656-916G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4667541 | |||||||
chr12:4667567 | G | A | 1 | a0001c0001t0029g0079 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.656-890G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4667567 | |||||||
chr12:4667631 | C | T | 1 | a0001c0001t0066g0193 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.656-826C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4667631 | |||||||
chr12:4667721 | A | G | 1 | a0001c0005t0019g0030 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.656-736A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4667721 | |||||||
chr12:4667752 | C | T | 16 | a0001c0001t0005g0018 a0001c0001t0005g0040 a0001c0001t0005g0047 others(13): Show |
19 | HG00642.hp1 HG00733.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.656-705C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4667752 | |||||||
chr12:4667832 | T | TA | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(120): Show |
162 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(159): Show |
intron_variant | MODIFIER | c.656-615dupA | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 4667832 | ||||||
chr12:4667862 | C | CA | 4 | a0001c0001t0026g0050 a0001c0001t0045g0199 a0001c0001t0063g0136 others(1): Show |
5 | HG01891.hp2 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.656-587dupA | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 4667862 | ||||||
chr12:4668064 | T | C | 3 | a0001c0001t0004g0094 a0001c0001t0004g0145 a0001c0001t0059g0194 |
3 | HG02486.hp2 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.656-393T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4668064 | |||||||
chr12:4668088 | C | T | 2 | a0001c0001t0003g0180 a0001c0001t0003g0232 |
2 | HG01081.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.656-369C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4668088 | |||||||
chr12:4668183 | C | T | 15 | a0001c0001t0005g0018 a0001c0001t0005g0040 a0001c0001t0005g0047 others(12): Show |
18 | HG00642.hp1 HG00733.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.656-274C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4668183 | |||||||
chr12:4668227 | G | A | 2 | a0001c0001t0026g0050 a0001c0001t0066g0193 |
3 | HG02976.hp2 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.656-230G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4668227 | |||||||
chr12:4668279 | C | T | 1 | a0004c0004t0062g0149 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.656-178C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4668279 | |||||||
chr12:4668308 | G | A | 10 | a0001c0001t0005g0018 a0001c0001t0005g0040 a0001c0001t0005g0047 others(7): Show |
13 | HG00642.hp1 HG00733.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.656-149G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4668308 | |||||||
chr12:4668446 | T | C | 1 | a0001c0001t0001g0209 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.656-11T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4668446 | |||||||
chr12:4668451 | C | T | 1 | a0001c0001t0002g0142 | 1 | HG02809.hp2 | splice_region_variant&intron_variant | LOW | c.656-6C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 6/10 | chr12 | 4668451 | |||||||
chr12:4668676 | C | T | 1 | a0001c0001t0036g0072 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.723+152C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 7/10 | chr12 | 4668676 | |||||||
chr12:4668696 | A | G | 4 | a0001c0001t0026g0050 a0001c0001t0045g0199 a0001c0001t0063g0136 others(1): Show |
5 | HG01891.hp2 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.723+172A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 7/10 | chr12 | 4668696 | |||||||
chr12:4668731 | A | G | 1 | a0001c0001t0002g0170 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.723+207A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 7/10 | chr12 | 4668731 | |||||||
chr12:4668844 | C | G | 1 | a0001c0001t0047g0062 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.723+320C>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 7/10 | chr12 | 4668844 | |||||||
chr12:4669135 | G | A | 1 | a0001c0001t0001g0031 | 2 | HG02683.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.724-606G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 7/10 | chr12 | 4669135 | |||||||
chr12:4669297 | C | G | 120 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(117): Show |
159 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(156): Show |
intron_variant | MODIFIER | c.724-444C>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 7/10 | chr12 | 4669297 | |||||||
chr12:4669461 | A | G | 120 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(117): Show |
154 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.724-280A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 7/10 | chr12 | 4669461 | |||||||
chr12:4669872 | A | G | 1 | a0001c0001t0005g0165 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.800+55A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4669872 | |||||||
chr12:4669921 | A | G | 118 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(115): Show |
152 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.800+104A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4669921 | |||||||
chr12:4669962 | C | T | 15 | a0001c0001t0004g0014 a0001c0001t0004g0024 a0001c0001t0004g0044 others(12): Show |
18 | HG00639.hp1 HG00733.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.800+145C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4669962 | |||||||
chr12:4670147 | A | G | 239 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(236): Show |
312 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(309): Show |
intron_variant | MODIFIER | c.800+330A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4670147 | |||||||
chr12:4670185 | T | G | 120 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(117): Show |
159 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(156): Show |
intron_variant | MODIFIER | c.800+368T>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4670185 | |||||||
chr12:4670244 | C | T | 8 | a0001c0001t0001g0008 a0001c0001t0001g0043 a0001c0001t0001g0053 others(5): Show |
14 | HG02145.hp2 HG02280.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.800+427C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4670244 | |||||||
chr12:4670323 | C | T | 2 | a0001c0001t0002g0252 a0001c0001t0002g0253 |
2 | HG01515.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.800+506C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4670323 | |||||||
chr12:4670658 | A | G | 1 | a0001c0001t0001g0202 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.800+841A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4670658 | |||||||
chr12:4670710 | A | G | 1 | a0001c0001t0045g0199 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.800+893A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4670710 | |||||||
chr12:4670771 | T | C | 122 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(119): Show |
161 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(158): Show |
intron_variant | MODIFIER | c.800+954T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4670771 | |||||||
chr12:4671008 | C | T | 2 | a0001c0001t0016g0058 a0001c0001t0016g0219 |
2 | HG03654.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.800+1191C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4671008 | |||||||
chr12:4671070 | G | T | 133 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(130): Show |
171 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.800+1253G>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4671070 | |||||||
chr12:4671074 | T | G | 1 | a0001c0001t0045g0199 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.800+1257T>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4671074 | |||||||
chr12:4671308 | C | T | 114 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(111): Show |
148 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.800+1491C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4671308 | |||||||
chr12:4671537 | A | G | 1 | a0001c0001t0001g0075 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.800+1720A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4671537 | |||||||
chr12:4671596 | T | C | 1 | a0001c0001t0002g0126 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.800+1779T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4671596 | |||||||
chr12:4671638 | A | C | 1 | a0001c0001t0002g0204 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.800+1821A>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4671638 | |||||||
chr12:4671644 | A | G | 2 | a0001c0001t0007g0078 a0001c0001t0007g0200 |
2 | HG02451.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.800+1827A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4671644 | |||||||
chr12:4671981 | G | A | 101 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(98): Show |
136 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(133): Show |
intron_variant | MODIFIER | c.800+2164G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4671981 | |||||||
chr12:4672054 | T | C | 3 | a0001c0001t0005g0018 a0001c0001t0005g0065 a0001c0001t0005g0144 |
5 | HG03139.hp2 HG03195.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.800+2237T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4672054 | |||||||
chr12:4672075 | G | A | 2 | a0001c0001t0001g0108 a0001c0001t0001g0120 |
2 | HG00639.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.800+2258G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4672075 | |||||||
chr12:4672115 | C | T | 2 | a0001c0001t0001g0117 a0001c0001t0001g0230 |
2 | HG00140.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.800+2298C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4672115 | |||||||
chr12:4672125 | G | A | 4 | a0001c0001t0002g0164 a0001c0001t0002g0177 a0001c0001t0002g0191 others(1): Show |
4 | HG00140.hp1 HG01081.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.800+2308G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4672125 | |||||||
chr12:4672141 | C | T | 2 | a0001c0001t0017g0052 a0001c0001t0017g0154 |
2 | HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.800+2324C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4672141 | |||||||
chr12:4672282 | T | G | 239 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(236): Show |
312 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(309): Show |
intron_variant | MODIFIER | c.800+2465T>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4672282 | |||||||
chr12:4672454 | C | G | 1 | a0001c0001t0001g0061 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.800+2637C>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4672454 | |||||||
chr12:4672479 | A | G | 1 | a0001c0001t0029g0079 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.800+2662A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4672479 | |||||||
chr12:4672661 | G | T | 1 | a0001c0001t0001g0186 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.800+2844G>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4672661 | |||||||
chr12:4672741 | T | C | 3 | a0004c0004t0060g0140 a0004c0004t0061g0251 a0004c0004t0062g0149 |
3 | HG01884.hp1 HG01884.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.800+2924T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4672741 | |||||||
chr12:4673023 | C | T | 1 | a0001c0001t0044g0195 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.800+3206C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4673023 | |||||||
chr12:4673151 | A | G | 101 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(98): Show |
136 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(133): Show |
intron_variant | MODIFIER | c.800+3334A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4673151 | |||||||
chr12:4673346 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.800+3529A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4673346 | |||||||
chr12:4673508 | A | T | 1 | a0001c0001t0001g0221 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.800+3691A>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4673508 | |||||||
chr12:4673512 | C | T | 1 | a0001c0001t0030g0125 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.800+3695C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4673512 | |||||||
chr12:4673521 | T | C | 83 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(80): Show |
113 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.800+3704T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4673521 | |||||||
chr12:4673549 | G | A | 1 | a0001c0001t0002g0234 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.800+3732G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4673549 | |||||||
chr12:4673598 | C | T | 8 | a0001c0001t0006g0034 a0001c0001t0006g0036 a0001c0001t0006g0122 others(5): Show |
12 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.800+3781C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4673598 | |||||||
chr12:4673616 | CAAGAT | C | 90 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(87): Show |
121 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.800+3804_800+3808d others(7): Show |
NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 4673616 | ||||||
chr12:4673815 | G | T | 2 | a0001c0001t0002g0100 a0001c0001t0002g0203 |
2 | NA18960.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.800+3998G>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4673815 | |||||||
chr12:4673836 | C | T | 4 | a0001c0001t0005g0042 a0001c0001t0005g0146 a0001c0001t0005g0192 others(1): Show |
5 | HG01891.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.800+4019C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4673836 | |||||||
chr12:4673854 | G | A | 1 | a0001c0001t0042g0238 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.800+4037G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4673854 | |||||||
chr12:4673933 | C | T | 1 | a0001c0001t0002g0105 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.800+4116C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4673933 | |||||||
chr12:4674103 | C | G | 1 | a0001c0001t0023g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.800+4286C>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4674103 | |||||||
chr12:4674238 | C | T | 1 | a0001c0001t0002g0160 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.800+4421C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4674238 | |||||||
chr12:4674475 | A | C | 1 | a0001c0001t0002g0231 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.800+4658A>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4674475 | |||||||
chr12:4674524 | T | C | 1 | a0001c0001t0002g0224 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.800+4707T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4674524 | |||||||
chr12:4674637 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0063 a0001c0001t0057g0015 |
4 | NA18971.hp1 NA18988.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.800+4820G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4674637 | |||||||
chr12:4674912 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.800+5095A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4674912 | |||||||
chr12:4674927 | A | G | 1 | a0001c0001t0002g0179 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.800+5110A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4674927 | |||||||
chr12:4675114 | C | T | 4 | a0001c0001t0002g0164 a0001c0001t0002g0177 a0001c0001t0002g0191 others(1): Show |
4 | HG00140.hp1 HG01081.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.800+5297C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4675114 | |||||||
chr12:4675142 | G | A | 2 | a0001c0001t0049g0236 a0001c0001t0050g0237 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.800+5325G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4675142 | |||||||
chr12:4675148 | C | G | 79 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(76): Show |
108 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.800+5331C>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4675148 | |||||||
chr12:4675149 | T | G | 1 | a0001c0001t0005g0137 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.800+5332T>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4675149 | |||||||
chr12:4675177 | G | C | 1 | a0001c0001t0001g0083 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.800+5360G>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4675177 | |||||||
chr12:4675319 | A | G | 145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
187 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(184): Show |
intron_variant | MODIFIER | c.800+5502A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4675319 | |||||||
chr12:4675336 | T | C | 3 | a0001c0001t0002g0038 a0001c0001t0002g0174 a0001c0001t0002g0187 |
4 | HG00438.hp2 HG02056.hp2 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.800+5519T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4675336 | |||||||
chr12:4675350 | A | G | 1 | a0001c0001t0052g0176 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.800+5533A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4675350 | |||||||
chr12:4675352 | C | T | 3 | a0001c0001t0026g0050 a0001c0001t0045g0199 a0001c0001t0066g0193 |
4 | HG02965.hp2 HG02976.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.800+5535C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4675352 | |||||||
chr12:4675409 | C | G | 25 | a0001c0001t0004g0014 a0001c0001t0004g0024 a0001c0001t0004g0033 others(22): Show |
28 | HG00639.hp1 HG00733.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.800+5592C>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4675409 | |||||||
chr12:4675416 | G | T | 3 | a0001c0001t0026g0050 a0001c0001t0045g0199 a0001c0001t0066g0193 |
4 | HG02965.hp2 HG02976.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.800+5599G>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4675416 | |||||||
chr12:4675464 | A | G | 94 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(91): Show |
125 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.800+5647A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4675464 | |||||||
chr12:4675592 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.800+5775C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4675592 | |||||||
chr12:4675808 | T | C | 3 | a0001c0001t0001g0003 a0001c0001t0001g0109 a0001c0001t0001g0175 |
8 | HG00642.hp2 HG00741.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.800+5991T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4675808 | |||||||
chr12:4675834 | A | G | 3 | a0004c0004t0060g0140 a0004c0004t0061g0251 a0004c0004t0062g0149 |
3 | HG01884.hp1 HG01884.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.800+6017A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4675834 | |||||||
chr12:4675851 | G | A | 239 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(236): Show |
312 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(309): Show |
intron_variant | MODIFIER | c.800+6034G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4675851 | |||||||
chr12:4675965 | C | T | 1 | a0001c0001t0045g0199 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.800+6148C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4675965 | |||||||
chr12:4676124 | G | A | 112 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(109): Show |
147 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.801-6081G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4676124 | |||||||
chr12:4676126 | T | C | 2 | a0001c0001t0017g0052 a0001c0001t0017g0154 |
2 | HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.801-6079T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4676126 | |||||||
chr12:4676170 | C | A | 2 | a0001c0001t0041g0088 a0001c0005t0019g0030 |
3 | HG01167.hp1 HG01169.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.801-6035C>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4676170 | |||||||
chr12:4676170 | C | G | 95 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(92): Show |
125 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.801-6035C>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4676170 | |||||||
chr12:4676197 | G | A | 8 | a0001c0001t0007g0070 a0001c0001t0007g0071 a0001c0001t0007g0078 others(5): Show |
8 | HG01952.hp2 HG02280.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.801-6008G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4676197 | |||||||
chr12:4676259 | G | A | 3 | a0001c0001t0001g0073 a0001c0001t0001g0217 a0001c0001t0001g0244 |
3 | NA18944.hp1 NA18963.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.801-5946G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4676259 | |||||||
chr12:4676327 | A | G | 26 | a0001c0001t0004g0014 a0001c0001t0004g0024 a0001c0001t0004g0033 others(23): Show |
29 | HG00639.hp1 HG00733.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.801-5878A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4676327 | |||||||
chr12:4676380 | A | G | 5 | a0001c0001t0005g0042 a0001c0001t0005g0146 a0001c0001t0005g0192 others(2): Show |
6 | HG01891.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.801-5825A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4676380 | |||||||
chr12:4676736 | G | A | 239 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(236): Show |
312 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(309): Show |
intron_variant | MODIFIER | c.801-5469G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4676736 | |||||||
chr12:4676792 | A | G | 1 | a0001c0001t0021g0115 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.801-5413A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4676792 | |||||||
chr12:4676905 | A | T | 1 | a0001c0001t0036g0072 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.801-5300A>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4676905 | |||||||
chr12:4676931 | C | T | 10 | a0001c0001t0001g0114 a0001c0001t0001g0256 a0001c0001t0007g0070 others(7): Show |
10 | HG01952.hp2 HG02071.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.801-5274C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4676931 | |||||||
chr12:4677062 | G | A | 99 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(96): Show |
133 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.801-5143G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4677062 | |||||||
chr12:4677116 | G | C | 12 | a0001c0001t0005g0018 a0001c0001t0005g0040 a0001c0001t0005g0047 others(9): Show |
15 | HG00642.hp1 HG00733.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.801-5089G>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4677116 | |||||||
chr12:4677131 | A | G | 2 | a0001c0001t0017g0052 a0001c0001t0017g0154 |
2 | HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.801-5074A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4677131 | |||||||
chr12:4677173 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.801-5032C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4677173 | |||||||
chr12:4677213 | G | A | 1 | a0001c0001t0044g0195 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.801-4992G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4677213 | |||||||
chr12:4677252 | G | A | 3 | a0001c0001t0026g0050 a0001c0001t0045g0199 a0001c0001t0066g0193 |
4 | HG02965.hp2 HG02976.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.801-4953G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4677252 | |||||||
chr12:4677319 | A | G | 1 | a0001c0001t0001g0256 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.801-4886A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4677319 | |||||||
chr12:4677330 | A | C | 2 | a0001c0001t0017g0052 a0001c0001t0017g0154 |
2 | HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.801-4875A>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4677330 | |||||||
chr12:4677394 | T | C | 1 | a0001c0001t0063g0136 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.801-4811T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4677394 | |||||||
chr12:4677480 | C | T | 2 | a0001c0001t0004g0248 a0001c0001t0004g0249 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.801-4725C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4677480 | |||||||
chr12:4677492 | G | A | 270 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(267): Show |
357 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(354): Show |
intron_variant | MODIFIER | c.801-4713G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4677492 | |||||||
chr12:4677685 | C | A | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(233): Show |
309 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(306): Show |
intron_variant | MODIFIER | c.801-4520C>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4677685 | |||||||
chr12:4677950 | A | G | 2 | a0001c0001t0001g0217 a0001c0001t0001g0244 |
2 | NA18944.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.801-4255A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4677950 | |||||||
chr12:4678214 | A | G | 3 | a0001c0001t0002g0148 a0001c0001t0002g0156 a0001c0001t0027g0089 |
3 | HG02895.hp1 HG02897.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.801-3991A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4678214 | |||||||
chr12:4678236 | A | G | 1 | a0001c0001t0017g0052 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.801-3969A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4678236 | |||||||
chr12:4678330 | A | G | 239 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(236): Show |
312 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(309): Show |
intron_variant | MODIFIER | c.801-3875A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4678330 | |||||||
chr12:4678440 | A | G | 1 | a0001c0001t0001g0220 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.801-3765A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4678440 | |||||||
chr12:4678450 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.801-3755A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4678450 | |||||||
chr12:4678601 | A | G | 3 | a0001c0001t0026g0050 a0001c0001t0045g0199 a0001c0001t0066g0193 |
4 | HG02965.hp2 HG02976.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.801-3604A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4678601 | |||||||
chr12:4678655 | G | A | 83 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(80): Show |
113 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.801-3550G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4678655 | |||||||
chr12:4678740 | A | G | 2 | a0001c0001t0017g0052 a0001c0001t0017g0154 |
2 | HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.801-3465A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4678740 | |||||||
chr12:4679060 | G | A | 3 | a0001c0001t0026g0050 a0001c0001t0045g0199 a0001c0001t0066g0193 |
4 | HG02965.hp2 HG02976.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.801-3145G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4679060 | |||||||
chr12:4679081 | T | G | 87 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(84): Show |
117 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.801-3124T>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4679081 | |||||||
chr12:4679200 | C | G | 44 | a0001c0001t0004g0014 a0001c0001t0004g0024 a0001c0001t0004g0033 others(41): Show |
51 | HG00639.hp1 HG00642.hp1 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.801-3005C>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4679200 | |||||||
chr12:4679266 | G | A | 1 | a0001c0001t0013g0212 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.801-2939G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4679266 | |||||||
chr12:4679312 | G | C | 1 | a0004c0004t0060g0140 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.801-2893G>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4679312 | |||||||
chr12:4679318 | G | A | 2 | a0001c0001t0004g0248 a0001c0001t0004g0249 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.801-2887G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4679318 | |||||||
chr12:4679472 | A | T | 1 | a0001c0001t0044g0195 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.801-2733A>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4679472 | |||||||
chr12:4679491 | A | C | 1 | a0001c0001t0044g0195 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.801-2714A>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4679491 | |||||||
chr12:4679671 | A | G | 1 | a0001c0001t0002g0242 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.801-2534A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4679671 | |||||||
chr12:4679905 | A | T | 1 | a0001c0001t0001g0241 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.801-2300A>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4679905 | |||||||
chr12:4679916 | C | G | 14 | a0001c0001t0005g0018 a0001c0001t0005g0040 a0001c0001t0005g0047 others(11): Show |
17 | HG00642.hp1 HG00733.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.801-2289C>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4679916 | |||||||
chr12:4679935 | G | A | 8 | a0001c0001t0007g0070 a0001c0001t0007g0071 a0001c0001t0007g0078 others(5): Show |
8 | HG01952.hp2 HG02280.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.801-2270G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4679935 | |||||||
chr12:4680229 | T | C | 7 | a0001c0001t0002g0017 a0001c0001t0002g0090 a0001c0001t0002g0104 others(4): Show |
9 | HG02080.hp2 HG02165.hp2 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.801-1976T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4680229 | |||||||
chr12:4680243 | T | TA | 101 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(98): Show |
136 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(133): Show |
intron_variant | MODIFIER | c.801-1955dupA | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 4680243 | ||||||
chr12:4680388 | A | T | 17 | a0001c0001t0005g0018 a0001c0001t0005g0040 a0001c0001t0005g0047 others(14): Show |
21 | HG00642.hp1 HG00733.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.801-1817A>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4680388 | |||||||
chr12:4680534 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.801-1671A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4680534 | |||||||
chr12:4680557 | G | A | 1 | a0001c0001t0005g0124 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.801-1648G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4680557 | |||||||
chr12:4680753 | G | C | 1 | a0001c0001t0029g0079 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.801-1452G>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4680753 | |||||||
chr12:4680803 | G | T | 1 | a0001c0001t0002g0215 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.801-1402G>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4680803 | |||||||
chr12:4681003 | T | C | 8 | a0001c0001t0007g0070 a0001c0001t0007g0071 a0001c0001t0007g0078 others(5): Show |
8 | HG01952.hp2 HG02280.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.801-1202T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4681003 | |||||||
chr12:4681140 | G | T | 1 | a0001c0001t0005g0055 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.801-1065G>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4681140 | |||||||
chr12:4681345 | T | C | 1 | a0002c0003t0009g0127 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.801-860T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4681345 | |||||||
chr12:4681414 | G | A | 3 | a0001c0001t0002g0148 a0001c0001t0002g0156 a0001c0001t0027g0089 |
3 | HG02895.hp1 HG02897.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.801-791G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4681414 | |||||||
chr12:4681414 | G | C | 1 | a0001c0001t0002g0225 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.801-791G>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4681414 | |||||||
chr12:4681425 | G | A | 18 | a0001c0001t0003g0019 a0001c0001t0003g0020 a0001c0001t0003g0021 others(15): Show |
28 | HG00544.hp1 HG00738.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.801-780G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4681425 | |||||||
chr12:4681437 | G | A | 1 | a0001c0001t0004g0102 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.801-768G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4681437 | |||||||
chr12:4681747 | C | T | 97 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(94): Show |
131 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.801-458C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4681747 | |||||||
chr12:4681801 | TA | T | 10 | a0001c0001t0005g0018 a0001c0001t0005g0040 a0001c0001t0005g0047 others(7): Show |
13 | HG00642.hp1 HG00733.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.801-400delA | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 4681801 | ||||||
chr12:4681943 | T | G | 1 | a0001c0001t0001g0110 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.801-262T>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4681943 | |||||||
chr12:4681988 | G | A | 8 | a0001c0001t0007g0070 a0001c0001t0007g0071 a0001c0001t0007g0078 others(5): Show |
8 | HG01952.hp2 HG02280.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.801-217G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 8/10 | chr12 | 4681988 | |||||||
chr12:4682364 | G | A | 1 | a0001c0001t0059g0194 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.896+64G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 9/10 | chr12 | 4682364 | |||||||
chr12:4682473 | A | T | 1 | a0001c0001t0037g0066 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.896+173A>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 9/10 | chr12 | 4682473 | |||||||
chr12:4682481 | G | A | 1 | a0001c0001t0004g0103 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.896+181G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 9/10 | chr12 | 4682481 | |||||||
chr12:4682496 | C | A | 97 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(94): Show |
131 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.896+196C>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 9/10 | chr12 | 4682496 | |||||||
chr12:4682507 | A | G | 126 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(123): Show |
160 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.896+207A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 9/10 | chr12 | 4682507 | |||||||
chr12:4682532 | A | G | 1 | a0001c0001t0001g0113 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.896+232A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 9/10 | chr12 | 4682532 | |||||||
chr12:4682676 | A | G | 25 | a0001c0001t0004g0014 a0001c0001t0004g0024 a0001c0001t0004g0033 others(22): Show |
28 | HG00639.hp1 HG00733.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.896+376A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 9/10 | chr12 | 4682676 | |||||||
chr12:4682877 | G | A | 1 | a0004c0004t0060g0140 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.896+577G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 9/10 | chr12 | 4682877 | |||||||
chr12:4682939 | G | A | 1 | a0001c0005t0019g0030 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.896+639G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 9/10 | chr12 | 4682939 | |||||||
chr12:4683096 | C | G | 1 | a0001c0001t0037g0066 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.896+796C>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 9/10 | chr12 | 4683096 | |||||||
chr12:4683180 | C | CA | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
253 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.896+894dupA | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 4683180 | ||||||
chr12:4683326 | T | C | 225 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(222): Show |
294 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.896+1026T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 9/10 | chr12 | 4683326 | |||||||
chr12:4683529 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.896+1229G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 9/10 | chr12 | 4683529 | |||||||
chr12:4683540 | A | C | 1 | a0001c0001t0002g0253 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.896+1240A>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 9/10 | chr12 | 4683540 | |||||||
chr12:4683567 | C | T | 1 | a0001c0001t0004g0172 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.896+1267C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 9/10 | chr12 | 4683567 | |||||||
chr12:4683707 | A | G | 4 | a0001c0001t0004g0033 a0001c0001t0004g0134 a0001c0001t0053g0033 others(1): Show |
4 | HG02572.hp1 HG02647.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.896+1407A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 9/10 | chr12 | 4683707 | |||||||
chr12:4683720 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.896+1420G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 9/10 | chr12 | 4683720 | |||||||
chr12:4683999 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.897-1260T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 9/10 | chr12 | 4683999 | |||||||
chr12:4684043 | T | C | 1 | a0001c0005t0019g0030 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.897-1216T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 9/10 | chr12 | 4684043 | |||||||
chr12:4684290 | C | G | 1 | a0001c0001t0001g0228 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.897-969C>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 9/10 | chr12 | 4684290 | |||||||
chr12:4684298 | G | A | 124 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(121): Show |
159 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.897-961G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 9/10 | chr12 | 4684298 | |||||||
chr12:4684387 | G | A | 1 | a0004c0004t0061g0251 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.897-872G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 9/10 | chr12 | 4684387 | |||||||
chr12:4684439 | C | T | 3 | a0001c0001t0026g0050 a0001c0001t0045g0199 a0001c0001t0066g0193 |
4 | HG02965.hp2 HG02976.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.897-820C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 9/10 | chr12 | 4684439 | |||||||
chr12:4684483 | A | G | 2 | a0001c0001t0018g0054 a0001c0001t0018g0064 |
2 | HG02109.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.897-776A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 9/10 | chr12 | 4684483 | |||||||
chr12:4684500 | T | TG | 16 | a0001c0001t0005g0018 a0001c0001t0005g0040 a0001c0001t0005g0047 others(13): Show |
20 | HG00642.hp1 HG00733.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.897-757dupG | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 4684500 | ||||||
chr12:4684504 | G | A | 3 | a0001c0001t0026g0050 a0001c0001t0045g0199 a0001c0001t0066g0193 |
4 | HG02965.hp2 HG02976.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.897-755G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 9/10 | chr12 | 4684504 | |||||||
chr12:4684533 | G | T | 4 | a0001c0001t0004g0033 a0001c0001t0004g0134 a0001c0001t0053g0033 others(1): Show |
4 | HG02572.hp1 HG02647.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.897-726G>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 9/10 | chr12 | 4684533 | |||||||
chr12:4684538 | A | G | 143 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(140): Show |
182 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.897-721A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 9/10 | chr12 | 4684538 | |||||||
chr12:4684541 | G | A | 1 | a0001c0001t0007g0070 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.897-718G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 9/10 | chr12 | 4684541 | |||||||
chr12:4684663 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.897-596A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 9/10 | chr12 | 4684663 | |||||||
chr12:4684780 | T | C | 1 | a0001c0001t0005g0124 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.897-479T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 9/10 | chr12 | 4684780 | |||||||
chr12:4684808 | A | ATT | 119 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(116): Show |
152 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.897-439_897-438dup others(2): Show |
NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 4684808 | ||||||
chr12:4684919 | T | A | 1 | a0001c0001t0001g0214 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.897-340T>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 9/10 | chr12 | 4684919 | |||||||
chr12:4685056 | C | T | 1 | a0004c0004t0061g0251 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.897-203C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 9/10 | chr12 | 4685056 | |||||||
chr12:4685135 | TA | T | 10 | a0001c0001t0001g0112 a0001c0001t0005g0192 a0001c0001t0007g0070 others(7): Show |
10 | HG01952.hp2 HG02280.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.897-112delA | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 4685135 | ||||||
chr12:4685185 | A | G | 126 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(123): Show |
164 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(161): Show |
intron_variant | MODIFIER | c.897-74A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 9/10 | chr12 | 4685185 | |||||||
chr12:4685370 | C | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0093 a0001c0001t0001g0246 others(1): Show |
7 | HG00558.hp2 NA18943.hp2 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.963+45C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 10/10 | chr12 | 4685370 | |||||||
chr12:4685453 | C | T | 1 | a0001c0001t0045g0199 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.963+128C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 10/10 | chr12 | 4685453 | |||||||
chr12:4685567 | A | G | 241 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(238): Show |
314 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.963+242A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 10/10 | chr12 | 4685567 | |||||||
chr12:4685679 | CTGAAGAA others(20): Show |
C | 100 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(97): Show |
133 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.963+356_963+382del others(27): Show |
NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 4685679 | ||||||
chr12:4685757 | A | G | 2 | a0001c0001t0016g0058 a0001c0001t0016g0219 |
2 | HG03654.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.963+432A>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 10/10 | chr12 | 4685757 | |||||||
chr12:4685787 | C | T | 5 | a0001c0001t0005g0042 a0001c0001t0005g0146 a0001c0001t0005g0192 others(2): Show |
6 | HG01891.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.963+462C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 10/10 | chr12 | 4685787 | |||||||
chr12:4685790 | G | T | 1 | a0001c0001t0006g0034 | 2 | HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.963+465G>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 10/10 | chr12 | 4685790 | |||||||
chr12:4685838 | G | A | 1 | a0004c0004t0062g0149 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.963+513G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 10/10 | chr12 | 4685838 | |||||||
chr12:4685877 | A | AC | 104 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(101): Show |
140 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(137): Show |
intron_variant | MODIFIER | c.963+552_963+553ins others(1): Show |
NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 10/10 | chr12 | 4685877 | |||||||
chr12:4685878 | T | A | 104 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(101): Show |
140 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(137): Show |
intron_variant | MODIFIER | c.963+553T>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 10/10 | chr12 | 4685878 | |||||||
chr12:4685878 | T | C | 138 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(135): Show |
175 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.963+553T>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 10/10 | chr12 | 4685878 | |||||||
chr12:4686125 | C | T | 1 | a0001c0001t0002g0095 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.963+800C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 10/10 | chr12 | 4686125 | |||||||
chr12:4686126 | G | A | 102 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(99): Show |
138 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.963+801G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 10/10 | chr12 | 4686126 | |||||||
chr12:4686235 | G | C | 18 | a0001c0001t0003g0019 a0001c0001t0003g0020 a0001c0001t0003g0021 others(15): Show |
28 | HG00544.hp1 HG00738.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.964-703G>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 10/10 | chr12 | 4686235 | |||||||
chr12:4686332 | T | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0135 |
3 | HG01109.hp2 HG02109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.964-606T>G | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 10/10 | chr12 | 4686332 | |||||||
chr12:4686424 | G | GT | 100 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(97): Show |
135 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.964-499dupT | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 4686424 | ||||||
chr12:4686505 | G | A | 102 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(99): Show |
137 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.964-433G>A | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 10/10 | chr12 | 4686505 | |||||||
chr12:4686601 | G | C | 2 | a0001c0001t0002g0224 a0001c0001t0002g0227 |
2 | HG01261.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.964-337G>C | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 10/10 | chr12 | 4686601 | |||||||
chr12:4686712 | C | T | 2 | a0001c0001t0017g0052 a0001c0001t0017g0154 |
2 | HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.964-226C>T | NDUFA9 | ENSG00000139180.11 | transcript | ENST00000266544.10 | protein_coding | 10/10 | chr12 | 4686712 |