Item | Value |
---|---|
geneid | 4729 |
ensemblid | ENSG00000178127.13 |
hgncid | 7717 |
symbol | NDUFV2 |
name | NADH:ubiquinone oxidoreductase core subunit V2 |
refseq_nuc | NM_021074.5 |
refseq_prot | NP_066552.2 |
ensembl_nuc | ENST00000318388.11 |
ensembl_prot | ENSP00000327268.6 |
mane_status | MANE Select |
chr | chr18 |
start | 9102699 |
end | 9134341 |
strand | + |
ver | v1.2 |
region | chr18:9102699-9134341 |
region5000 | chr18:9097699-9139341 |
regionname0 | NDUFV2_chr18_9102699_9134341 |
regionname5000 | NDUFV2_chr18_9097699_9139341 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 249 | 258 | 70 | 50 | 99 | 13 | 25 | 68 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | MFFSA others(244): Show |
chr18 | 9097699 | 9139341 |
a0002 | 1/0 | 249 | 107 | 20 | 22 | 52 | 3 | 9 | 45 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | MFFSA others(244): Show |
chr18 | 9097699 | 9139341 |
a0003 | 0/0 | 249 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | MFFSA others(244): Show |
chr18 | 9097699 | 9139341 |
a0004 | 0/0 | 249 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | MFFSA others(244): Show |
chr18 | 9097699 | 9139341 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 747 | 233 | 54 | 44 | 99 | 12 | 23 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | ATGTT others(742): Show |
chr18 | 9097699 | 9139341 | ||
a0001c0003 | 0/0 | 747 | 25 | 16 | 6 | 0 | 1 | 2 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | ATGTT others(742): Show |
chr18 | 9097699 | 9139341 | ||
a0002c0002 | 1/0 | 747 | 107 | 20 | 22 | 52 | 3 | 9 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | ATGTT others(742): Show |
chr18 | 9097699 | 9139341 | ||
a0003c0004 | 0/0 | 747 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | ATGTT others(742): Show |
chr18 | 9097699 | 9139341 | ||
a0004c0005 | 0/0 | 747 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | ATGTT others(742): Show |
chr18 | 9097699 | 9139341 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 857 | 230 | 52 | 43 | 99 | 12 | 23 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | ATTCT others(852): Show |
chr18 | 9097699 | 9139341 |
a0001c0001t0002 | 0/0 | 857 | 2 | 1 | 1 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | ATTCT others(852): Show |
chr18 | 9097699 | 9139341 |
a0001c0001t0003 | 0/0 | 857 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | ATTCT others(852): Show |
chr18 | 9097699 | 9139341 |
a0001c0003t0001 | 0/0 | 857 | 25 | 16 | 6 | 0 | 1 | 2 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | ATTCT others(852): Show |
chr18 | 9097699 | 9139341 |
a0002c0002t0001 | 1/0 | 857 | 107 | 20 | 22 | 52 | 3 | 9 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | ATTCT others(852): Show |
chr18 | 9097699 | 9139341 |
a0003c0004t0001 | 0/0 | 857 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | ATTCT others(852): Show |
chr18 | 9097699 | 9139341 |
a0004c0005t0001 | 0/0 | 857 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | ATTCT others(852): Show |
chr18 | 9097699 | 9139341 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 18 | 3 | 1 | 14 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0003 | 0/0 | 17 | 3 | 5 | 7 | 1 | 1 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0004 | 0/0 | 13 | 0 | 1 | 6 | 2 | 4 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0005 | 0/0 | 12 | 0 | 6 | 3 | 2 | 1 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0023 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0024 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0026 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0049 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0136 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0001t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0003t0001g0009 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0003t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0003t0001g0018 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0003t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0003t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0003t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0003t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0003t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0003t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0003t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0003t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0003t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0003t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0001c0003t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0002c0002t0001g0001 | 1/0 | 41 | 6 | 4 | 27 | 1 | 2 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0002c0002t0001g0006 | 0/0 | 6 | 0 | 4 | 0 | 0 | 2 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0002c0002t0001g0007 | 0/0 | 6 | 2 | 0 | 3 | 0 | 1 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0002c0002t0001g0008 | 0/0 | 5 | 2 | 1 | 0 | 1 | 1 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0002c0002t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0002c0002t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0002c0002t0001g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0002c0002t0001g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0002c0002t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0002c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0002c0002t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0002c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0002c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0002c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0002c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0002c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0002c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0002c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0002c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0002c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0002c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0003c0004t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
a0004c0005t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0003 | t0001 | g0185 | EUR | GBR | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0177 | EUR | GBR | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0008 | EUR | FIN | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | FIN | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG00323 | hp1 | a0002 | c0002 | t0001 | g0001 | EUR | FIN | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG00423 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG00609 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG00621 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG00733 | hp1 | a0001 | c0003 | t0001 | g0115 | AMR | PUR | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0066 | AMR | PUR | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0016 | AMR | PUR | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01069 | hp1 | a0002 | c0002 | t0001 | g0064 | AMR | PUR | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01070 | hp1 | a0002 | c0002 | t0001 | g0027 | AMR | PUR | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01070 | hp2 | a0001 | c0003 | t0001 | g0186 | AMR | PUR | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0027 | AMR | PUR | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0017 | AMR | PUR | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01074 | hp2 | a0002 | c0002 | t0001 | g0077 | AMR | PUR | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01081 | hp2 | a0001 | c0003 | t0001 | g0009 | AMR | PUR | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01099 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01109 | hp2 | a0002 | c0002 | t0001 | g0056 | AMR | PUR | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0079 | AMR | PUR | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01167 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01168 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01169 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01169 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01243 | hp1 | a0001 | c0003 | t0001 | g0018 | AMR | PUR | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01255 | hp2 | a0001 | c0003 | t0001 | g0031 | AMR | CLM | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01261 | hp2 | a0002 | c0002 | t0001 | g0062 | AMR | CLM | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0017 | AMR | CLM | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0130 | EUR | IBS | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01891 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | ACB | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0017 | AMR | PEL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0016 | AMR | PEL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02004 | hp1 | a0001 | c0003 | t0001 | g0085 | AMR | PEL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02071 | hp1 | a0002 | c0002 | t0001 | g0054 | EAS | KHV | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02083 | hp2 | a0002 | c0002 | t0001 | g0153 | EAS | KHV | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02129 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02148 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | PEL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CDX | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CDX | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CDX | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | ACB | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02258 | hp1 | a0003 | c0004 | t0001 | g0039 | AFR | ACB | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02258 | hp2 | a0002 | c0002 | t0001 | g0008 | AFR | ACB | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02300 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PEL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02451 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | ACB | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02451 | hp2 | a0001 | c0003 | t0001 | g0015 | AFR | ACB | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02572 | hp2 | a0001 | c0003 | t0001 | g0187 | AFR | GWD | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02615 | hp1 | a0002 | c0002 | t0001 | g0029 | AFR | GWD | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02622 | hp2 | a0001 | c0003 | t0001 | g0009 | AFR | GWD | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02683 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02717 | hp1 | a0002 | c0002 | t0001 | g0029 | AFR | GWD | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02717 | hp2 | a0001 | c0003 | t0001 | g0084 | AFR | GWD | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02723 | hp2 | a0001 | c0003 | t0001 | g0083 | AFR | GWD | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | GWD | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02895 | hp1 | a0002 | c0002 | t0001 | g0058 | AFR | GWD | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02896 | hp2 | a0002 | c0002 | t0001 | g0059 | AFR | GWD | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0164 | AFR | ESN | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02965 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | ESN | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02970 | hp2 | a0002 | c0002 | t0001 | g0060 | AFR | ESN | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0006 | SAS | PJL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03041 | hp2 | a0002 | c0002 | t0001 | g0081 | AFR | GWD | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | MSL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | MSL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03139 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | ESN | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03195 | hp2 | a0003 | c0004 | t0001 | g0039 | AFR | ESN | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03225 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | MSL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0008 | SAS | PJL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03453 | hp2 | a0001 | c0003 | t0001 | g0086 | AFR | MSL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03486 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | MSL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03490 | hp1 | a0002 | c0002 | t0001 | g0068 | SAS | PJL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03516 | hp1 | a0001 | c0003 | t0001 | g0015 | AFR | ESN | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03516 | hp2 | a0001 | c0003 | t0001 | g0082 | AFR | ESN | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03540 | hp1 | a0001 | c0003 | t0001 | g0015 | AFR | GWD | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03579 | hp1 | a0001 | c0003 | t0001 | g0018 | AFR | MSL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | MSL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03654 | hp1 | a0001 | c0003 | t0001 | g0183 | SAS | PJL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03669 | hp2 | a0002 | c0002 | t0001 | g0006 | SAS | PJL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03688 | hp1 | a0002 | c0002 | t0001 | g0065 | SAS | STU | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | STU | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03704 | hp1 | a0001 | c0003 | t0001 | g0031 | SAS | PJL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0071 | SAS | PJL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03831 | hp2 | a0002 | c0002 | t0001 | g0007 | SAS | BEB | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | STU | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | BEB | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | STU | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | YRI | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18522 | hp2 | a0002 | c0002 | t0001 | g0052 | AFR | YRI | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CHB | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHB | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18906 | hp1 | a0002 | c0002 | t0001 | g0067 | AFR | YRI | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18906 | hp2 | a0001 | c0003 | t0001 | g0009 | AFR | YRI | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18939 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18941 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18942 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18943 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18953 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18956 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18957 | hp1 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18963 | hp2 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18967 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18973 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18974 | hp2 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18977 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18980 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18981 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18982 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18983 | hp1 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18984 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18985 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18990 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18994 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18999 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19001 | hp1 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19001 | hp2 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19003 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19004 | hp2 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19005 | hp1 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19006 | hp2 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19012 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19030 | hp1 | a0002 | c0002 | t0001 | g0050 | AFR | LWK | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19043 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | LWK | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19043 | hp2 | a0001 | c0003 | t0001 | g0009 | AFR | LWK | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19055 | hp2 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19057 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19058 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19064 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19065 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19076 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19077 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19079 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19081 | hp2 | a0004 | c0005 | t0001 | g0032 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19082 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19084 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | YRI | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | YRI | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA20129 | hp1 | a0001 | c0003 | t0001 | g0184 | AFR | ASW | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ASW | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | TSI | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0057 | EUR | TSI | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0025 | EUR | TSI | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0016 | AMR | CLM | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02486 | hp2 | a0001 | c0003 | t0001 | g0018 | AFR | ACB | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02559 | hp1 | a0001 | c0003 | t0001 | g0087 | AFR | ACB | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03471 | hp1 | a0001 | c0003 | t0001 | g0009 | AFR | MSL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | MSL | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG06807 | hp1 | a0002 | c0002 | t0001 | g0008 | AFR | USA | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | USA | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA18955 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA20300 | hp1 | a0002 | c0002 | t0001 | g0156 | AFR | USA | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | USA | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0136 | REF | REF | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0001 | REF | REF | NDUFV2_chr18_9097699_9139341 | NDUFV2 | chr18 | 9097699 | 9139341 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:9117869 | T | C | 3 | a0001 a0003 a0004 |
260 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(257): Show |
missense_variant | MODERATE | c.86T>C | p.Val29Ala | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 2/8 | 131/857 | 86/750 | 29/249 | chr18 | 9117869 | |||
chr18:9117901 | G | A | 1 | a0003 | 2 | HG02258.hp1 HG03195.hp2 |
missense_variant&splice_region_variant | MODERATE | c.118G>A | p.Val40Met | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 2/8 | 163/857 | 118/750 | 40/249 | chr18 | 9117901 | |||
chr18:9119326 | C | T | 1 | a0004 | 1 | NA19081.hp2 | missense_variant&splice_region_variant | MODERATE | c.121C>T | p.His41Tyr | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 3/8 | 166/857 | 121/750 | 41/249 | chr18 | 9119326 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:9119491 | A | T | 1 | a0001c0003 | 25 | HG00140.hp1 HG00733.hp1 HG01070.hp2 others(22): Show |
synonymous_variant | LOW | c.201A>T | p.Val67Val | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 4/8 | 246/857 | 201/750 | 67/249 | chr18 | 9119491 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:9102714 | G | T | 1 | a0001c0001t0002 | 2 | HG01167.hp1 HG02257.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-30G>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/8 | chr18 | 9102714 | |||||||
chr18:9102731 | A | G | 1 | a0001c0001t0003 | 1 | HG02922.hp2 | 5_prime_UTR_variant | MODIFIER | c.-13A>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/8 | 13 | chr18 | 9102731 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:9102953 | C | G | 1 | a0001c0001t0001g0191 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.54+156C>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9102953 | |||||||
chr18:9103014 | G | A | 1 | a0001c0003t0001g0015 | 3 | HG02451.hp2 HG03516.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.54+217G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9103014 | |||||||
chr18:9103153 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0189 a0001c0001t0001g0190 |
6 | HG01106.hp1 HG01884.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.54+356C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9103153 | |||||||
chr18:9103206 | G | C | 1 | a0002c0002t0001g0050 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.54+409G>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9103206 | |||||||
chr18:9103285 | A | C | 1 | a0001c0001t0001g0190 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.54+488A>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9103285 | |||||||
chr18:9103314 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.54+517C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9103314 | |||||||
chr18:9103323 | C | T | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(132): Show |
231 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.54+526C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9103323 | |||||||
chr18:9103766 | G | A | 94 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(91): Show |
164 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.54+969G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9103766 | |||||||
chr18:9103799 | C | G | 15 | a0001c0003t0001g0009 a0001c0003t0001g0015 a0001c0003t0001g0018 others(12): Show |
24 | HG00140.hp1 HG01070.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.54+1002C>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9103799 | |||||||
chr18:9103858 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.54+1061A>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9103858 | |||||||
chr18:9103900 | T | C | 1 | a0001c0001t0001g0043 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.54+1103T>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9103900 | |||||||
chr18:9103966 | A | G | 4 | a0001c0001t0001g0010 a0001c0001t0001g0152 a0001c0001t0001g0154 others(1): Show |
8 | HG02027.hp2 HG02040.hp1 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.54+1169A>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9103966 | |||||||
chr18:9103971 | G | A | 1 | a0001c0001t0001g0043 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.54+1174G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9103971 | |||||||
chr18:9104006 | G | GT | 18 | a0001c0001t0001g0002 a0001c0001t0001g0048 a0001c0001t0001g0049 others(15): Show |
37 | HG00140.hp2 HG00639.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.54+1210dupT | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 9104006 | ||||||
chr18:9104084 | A | G | 3 | a0001c0001t0001g0042 a0001c0001t0001g0151 a0001c0001t0001g0188 |
4 | HG00423.hp2 HG02071.hp2 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.54+1287A>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9104084 | |||||||
chr18:9104206 | G | GC | 18 | a0001c0001t0001g0002 a0001c0001t0001g0048 a0001c0001t0001g0049 others(15): Show |
37 | HG00140.hp2 HG00639.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.54+1411dupC | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 9104206 | ||||||
chr18:9104285 | G | A | 33 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0019 others(30): Show |
60 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.54+1488G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9104285 | |||||||
chr18:9104297 | A | G | 1 | a0002c0002t0001g0081 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.54+1500A>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9104297 | |||||||
chr18:9104370 | T | C | 1 | a0001c0001t0001g0103 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.54+1573T>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9104370 | |||||||
chr18:9104403 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.54+1606G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9104403 | |||||||
chr18:9104967 | C | T | 2 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.54+2170C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9104967 | |||||||
chr18:9105105 | T | C | 5 | a0001c0003t0001g0183 a0001c0003t0001g0184 a0001c0003t0001g0185 others(2): Show |
5 | HG00140.hp1 HG01070.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.54+2308T>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9105105 | |||||||
chr18:9105110 | C | T | 143 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(140): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.54+2313C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9105110 | |||||||
chr18:9105255 | C | G | 1 | a0001c0001t0001g0102 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.54+2458C>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9105255 | |||||||
chr18:9105524 | T | C | 15 | a0001c0003t0001g0009 a0001c0003t0001g0015 a0001c0003t0001g0018 others(12): Show |
24 | HG00140.hp1 HG01070.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.54+2727T>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9105524 | |||||||
chr18:9105761 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.54+2964G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9105761 | |||||||
chr18:9105770 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.54+2973C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9105770 | |||||||
chr18:9105870 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.54+3073C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9105870 | |||||||
chr18:9106080 | G | C | 1 | a0001c0001t0001g0106 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.54+3283G>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9106080 | |||||||
chr18:9106180 | T | C | 2 | a0001c0001t0001g0044 a0001c0001t0001g0158 |
3 | HG02647.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.54+3383T>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9106180 | |||||||
chr18:9106286 | G | T | 1 | a0001c0001t0001g0147 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.54+3489G>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9106286 | |||||||
chr18:9106539 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.54+3742A>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9106539 | |||||||
chr18:9106566 | A | C | 1 | a0001c0001t0002g0079 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.54+3769A>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9106566 | |||||||
chr18:9106777 | A | T | 1 | a0001c0001t0001g0041 | 2 | NA18977.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.54+3980A>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9106777 | |||||||
chr18:9106786 | T | C | 2 | a0001c0001t0001g0045 a0001c0001t0001g0159 |
3 | HG02109.hp2 HG02572.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.54+3989T>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9106786 | |||||||
chr18:9106913 | C | CCTT | 145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
250 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.54+4118_54+4119ins others(3): Show |
NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 9106913 | ||||||
chr18:9106985 | G | GGGC | 2 | a0001c0001t0001g0030 a0001c0001t0001g0157 |
3 | HG01891.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.54+4188_54+4189ins others(3): Show |
NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9106985 | |||||||
chr18:9106986 | A | C | 2 | a0001c0001t0001g0030 a0001c0001t0001g0157 |
3 | HG01891.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.54+4189A>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9106986 | |||||||
chr18:9106987 | T | C | 2 | a0001c0001t0001g0030 a0001c0001t0001g0157 |
3 | HG01891.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.54+4190T>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9106987 | |||||||
chr18:9106990 | TCC | T | 2 | a0001c0001t0001g0030 a0001c0001t0001g0157 |
3 | HG01891.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.54+4194_54+4195del others(2): Show |
NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9106990 | |||||||
chr18:9107031 | C | A | 5 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0157 others(2): Show |
9 | HG01167.hp1 HG01884.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.54+4234C>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9107031 | |||||||
chr18:9107069 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.54+4272G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9107069 | |||||||
chr18:9107092 | A | C | 1 | a0001c0001t0001g0146 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.54+4295A>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9107092 | |||||||
chr18:9107155 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.54+4358A>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9107155 | |||||||
chr18:9107193 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.54+4396C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9107193 | |||||||
chr18:9107269 | T | C | 4 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0157 others(1): Show |
8 | HG01884.hp2 HG01891.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.54+4472T>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9107269 | |||||||
chr18:9107421 | A | G | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
4 | HG01361.hp1 HG01952.hp1 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.54+4624A>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9107421 | |||||||
chr18:9107514 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.54+4717T>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9107514 | |||||||
chr18:9107528 | G | A | 1 | a0001c0003t0001g0082 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.54+4731G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9107528 | |||||||
chr18:9107601 | A | G | 3 | a0001c0001t0001g0025 a0001c0001t0001g0144 a0001c0001t0001g0145 |
5 | HG01069.hp2 HG01071.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.54+4804A>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9107601 | |||||||
chr18:9107817 | T | C | 15 | a0001c0003t0001g0009 a0001c0003t0001g0015 a0001c0003t0001g0018 others(12): Show |
24 | HG00140.hp1 HG01070.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.54+5020T>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9107817 | |||||||
chr18:9108174 | G | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0157 others(1): Show |
8 | HG01884.hp2 HG01891.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.54+5377G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9108174 | |||||||
chr18:9108266 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.54+5469C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9108266 | |||||||
chr18:9108689 | A | AT | 21 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0048 others(18): Show |
44 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.54+5911dupT | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 9108689 | ||||||
chr18:9108689 | AT | A | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): Show |
193 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.54+5911delT | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 9108689 | ||||||
chr18:9108701 | T | C | 1 | a0001c0001t0001g0107 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.54+5904T>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9108701 | |||||||
chr18:9108743 | T | G | 2 | a0001c0001t0001g0045 a0001c0001t0001g0159 |
3 | HG02109.hp2 HG02572.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.54+5946T>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9108743 | |||||||
chr18:9108776 | T | C | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(147): Show |
259 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.54+5979T>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9108776 | |||||||
chr18:9108943 | G | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0157 others(1): Show |
8 | HG01884.hp2 HG01891.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.54+6146G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9108943 | |||||||
chr18:9108981 | C | A | 1 | a0001c0001t0001g0190 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.54+6184C>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9108981 | |||||||
chr18:9109102 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.54+6305T>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9109102 | |||||||
chr18:9109191 | T | G | 1 | a0001c0001t0001g0106 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.54+6394T>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9109191 | |||||||
chr18:9109486 | T | G | 121 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(118): Show |
213 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.54+6689T>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9109486 | |||||||
chr18:9109579 | C | A | 1 | a0001c0001t0001g0163 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.54+6782C>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9109579 | |||||||
chr18:9109781 | C | T | 3 | a0001c0001t0001g0160 a0001c0001t0001g0163 a0001c0003t0001g0086 |
3 | HG02976.hp1 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.54+6984C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9109781 | |||||||
chr18:9109900 | G | GA | 8 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0001g0108 others(5): Show |
12 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.54+7112dupA | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 9109900 | ||||||
chr18:9109906 | A | C | 1 | a0001c0001t0001g0190 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.54+7109A>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9109906 | |||||||
chr18:9110122 | A | G | 2 | a0001c0001t0001g0160 a0001c0001t0001g0163 |
2 | HG02976.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.54+7325A>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9110122 | |||||||
chr18:9110126 | A | AG | 18 | a0001c0001t0001g0002 a0001c0001t0001g0048 a0001c0001t0001g0049 others(15): Show |
37 | HG00140.hp2 HG00639.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.54+7334dupG | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 9110126 | ||||||
chr18:9110129 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0157 |
3 | HG01891.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.54+7332G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9110129 | |||||||
chr18:9110217 | C | G | 1 | a0001c0003t0001g0085 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.54+7420C>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9110217 | |||||||
chr18:9110318 | G | A | 148 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(145): Show |
257 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.55-7520G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9110318 | |||||||
chr18:9110335 | T | A | 1 | a0001c0001t0001g0080 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.55-7503T>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9110335 | |||||||
chr18:9110346 | T | TGATATTC others(296): Show |
1 | a0001c0001t0001g0100 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.55-7482_55-7481ins others(303): Show |
NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 9110346 | ||||||
chr18:9110478 | C | G | 2 | a0001c0001t0001g0139 a0001c0001t0001g0158 |
2 | HG02165.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.55-7360C>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9110478 | |||||||
chr18:9110555 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.55-7283C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9110555 | |||||||
chr18:9110610 | C | G | 1 | a0001c0001t0001g0101 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.55-7228C>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9110610 | |||||||
chr18:9110871 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.55-6967C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9110871 | |||||||
chr18:9110961 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.55-6877A>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9110961 | |||||||
chr18:9110978 | C | G | 1 | a0001c0001t0001g0182 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.55-6860C>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9110978 | |||||||
chr18:9111139 | G | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
176 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.55-6699G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9111139 | |||||||
chr18:9111150 | A | G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0165 |
6 | HG01243.hp2 HG02257.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.55-6688A>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9111150 | |||||||
chr18:9111182 | G | T | 1 | a0001c0001t0002g0079 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.55-6656G>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9111182 | |||||||
chr18:9111255 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.55-6583T>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9111255 | |||||||
chr18:9111440 | T | C | 16 | a0001c0001t0001g0040 a0001c0003t0001g0009 a0001c0003t0001g0015 others(13): Show |
26 | HG00140.hp1 HG01070.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.55-6398T>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9111440 | |||||||
chr18:9111498 | GGCTCACT others(583): Show |
G | 4 | a0001c0001t0001g0080 a0001c0001t0001g0161 a0001c0001t0001g0166 others(1): Show |
4 | HG02922.hp2 HG03098.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.55-6324_55-5735del | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 9111498 | ||||||
chr18:9111626 | A | T | 1 | a0002c0002t0001g0001 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.55-6212A>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9111626 | |||||||
chr18:9111648 | C | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0034 others(2): Show |
8 | HG01168.hp2 HG01361.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.55-6190C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9111648 | |||||||
chr18:9111676 | G | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0157 others(1): Show |
8 | HG01884.hp2 HG01891.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.55-6162G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9111676 | |||||||
chr18:9111726 | G | C | 1 | a0002c0002t0001g0001 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.55-6112G>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9111726 | |||||||
chr18:9112017 | G | GT | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(97): Show |
161 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(158): Show |
intron_variant | MODIFIER | c.55-5802dupT | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 9112017 | ||||||
chr18:9112017 | G | GTT | 44 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(41): Show |
56 | HG00140.hp1 HG00423.hp2 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.55-5803_55-5802dup others(2): Show |
NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 9112017 | ||||||
chr18:9112017 | G | GTTT | 5 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0160 others(2): Show |
8 | HG01243.hp1 HG01891.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.55-5804_55-5802dup others(3): Show |
NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 9112017 | ||||||
chr18:9112084 | T | C | 102 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(99): Show |
175 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.55-5754T>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9112084 | |||||||
chr18:9112167 | C | T | 6 | a0001c0001t0001g0046 a0001c0001t0001g0080 a0001c0001t0001g0161 others(3): Show |
7 | HG02055.hp2 HG02922.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.55-5671C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9112167 | |||||||
chr18:9112180 | G | A | 1 | a0002c0002t0001g0081 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.55-5658G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9112180 | |||||||
chr18:9112361 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.55-5477A>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9112361 | |||||||
chr18:9113032 | A | G | 1 | a0002c0002t0001g0076 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.55-4806A>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9113032 | |||||||
chr18:9113232 | C | G | 16 | a0001c0001t0001g0040 a0001c0003t0001g0009 a0001c0003t0001g0015 others(13): Show |
26 | HG00140.hp1 HG01070.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.55-4606C>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9113232 | |||||||
chr18:9113691 | T | C | 2 | a0001c0001t0001g0046 a0001c0001t0001g0190 |
3 | HG01106.hp1 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.55-4147T>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9113691 | |||||||
chr18:9113706 | C | A | 1 | a0001c0001t0001g0112 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.55-4132C>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9113706 | |||||||
chr18:9113816 | C | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0190 |
3 | HG01106.hp1 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.55-4022C>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9113816 | |||||||
chr18:9113913 | G | T | 1 | a0002c0002t0001g0029 | 2 | HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.55-3925G>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9113913 | |||||||
chr18:9113944 | T | C | 1 | a0002c0002t0001g0052 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.55-3894T>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9113944 | |||||||
chr18:9113972 | C | T | 1 | a0003c0004t0001g0039 | 2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.55-3866C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9113972 | |||||||
chr18:9114069 | T | C | 20 | a0001c0001t0001g0002 a0001c0001t0001g0048 a0001c0001t0001g0053 others(17): Show |
38 | HG00140.hp2 HG00639.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.55-3769T>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9114069 | |||||||
chr18:9114098 | T | G | 159 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.55-3740T>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9114098 | |||||||
chr18:9114106 | A | AGCTGTTC others(6): Show |
9 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0097 others(6): Show |
12 | HG00423.hp2 HG00621.hp2 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.55-3727_55-3715dup others(13): Show |
NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 9114106 | ||||||
chr18:9114236 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.55-3602G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9114236 | |||||||
chr18:9114398 | A | C | 1 | a0001c0001t0001g0163 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.55-3440A>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9114398 | |||||||
chr18:9114445 | CTT | C | 4 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0157 others(1): Show |
8 | HG01884.hp2 HG01891.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.55-3374_55-3373del others(2): Show |
NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 9114445 | ||||||
chr18:9114445 | CTTTT | C | 132 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(129): Show |
236 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.55-3376_55-3373del others(4): Show |
NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 9114445 | ||||||
chr18:9114445 | CTTTTT | C | 10 | a0001c0001t0001g0044 a0001c0001t0001g0089 a0001c0001t0001g0090 others(7): Show |
11 | HG01928.hp2 HG02004.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.55-3377_55-3373del others(5): Show |
NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 9114445 | ||||||
chr18:9114545 | T | C | 1 | a0001c0001t0001g0005 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.55-3293T>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9114545 | |||||||
chr18:9114757 | C | G | 1 | a0001c0003t0001g0185 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.55-3081C>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9114757 | |||||||
chr18:9114824 | G | A | 1 | a0001c0003t0001g0115 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.55-3014G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9114824 | |||||||
chr18:9115081 | T | G | 1 | a0002c0002t0001g0056 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.55-2757T>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9115081 | |||||||
chr18:9115181 | A | C | 1 | a0002c0002t0001g0075 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.55-2657A>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9115181 | |||||||
chr18:9115306 | A | T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0159 |
3 | HG02109.hp2 HG02572.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.55-2532A>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9115306 | |||||||
chr18:9115568 | C | G | 1 | a0001c0001t0001g0038 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.55-2270C>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9115568 | |||||||
chr18:9115791 | G | C | 1 | a0001c0003t0001g0083 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.55-2047G>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9115791 | |||||||
chr18:9115854 | G | A | 1 | a0001c0003t0001g0018 | 3 | HG01243.hp1 HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.55-1984G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9115854 | |||||||
chr18:9115859 | C | CA | 6 | a0001c0001t0001g0025 a0001c0001t0001g0037 a0001c0001t0001g0116 others(3): Show |
9 | HG01516.hp1 HG01517.hp1 NA18967.hp2 others(6): Show |
intron_variant | MODIFIER | c.55-1966dupA | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 9115859 | ||||||
chr18:9115979 | A | G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0165 |
6 | HG01243.hp2 HG02257.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.55-1859A>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9115979 | |||||||
chr18:9116082 | T | C | 9 | a0002c0002t0001g0006 a0002c0002t0001g0008 a0002c0002t0001g0056 others(6): Show |
18 | HG00280.hp1 HG00735.hp1 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.55-1756T>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9116082 | |||||||
chr18:9116303 | A | G | 3 | a0001c0003t0001g0018 a0001c0003t0001g0082 a0001c0003t0001g0083 |
5 | HG01243.hp1 HG02486.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.55-1535A>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9116303 | |||||||
chr18:9116356 | C | CCTT | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(148): Show |
260 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.55-1481_55-1479dup others(3): Show |
NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 9116356 | ||||||
chr18:9116486 | A | G | 1 | a0001c0001t0002g0079 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.55-1352A>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9116486 | |||||||
chr18:9116824 | C | T | 14 | a0001c0001t0001g0002 a0001c0001t0001g0048 a0001c0001t0001g0049 others(11): Show |
33 | HG00140.hp2 HG00639.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.55-1014C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9116824 | |||||||
chr18:9117038 | C | CT | 5 | a0001c0001t0001g0042 a0001c0001t0001g0161 a0001c0001t0001g0166 others(2): Show |
6 | HG00423.hp2 HG02071.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.55-784dupT | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 9117038 | ||||||
chr18:9117038 | CT | C | 34 | a0001c0001t0001g0002 a0001c0001t0001g0048 a0001c0001t0001g0049 others(31): Show |
62 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.55-784delT | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr18 | 9117038 | ||||||
chr18:9117059 | C | T | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | HG01123.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.55-779C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9117059 | |||||||
chr18:9117151 | C | T | 1 | a0002c0002t0001g0074 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.55-687C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9117151 | |||||||
chr18:9117165 | T | C | 1 | a0001c0001t0001g0117 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.55-673T>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9117165 | |||||||
chr18:9117290 | C | G | 16 | a0001c0003t0001g0009 a0001c0003t0001g0015 a0001c0003t0001g0018 others(13): Show |
25 | HG00140.hp1 HG00733.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.55-548C>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9117290 | |||||||
chr18:9117564 | C | T | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(103): Show |
179 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.55-274C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9117564 | |||||||
chr18:9117619 | A | C | 1 | a0001c0001t0001g0129 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.55-219A>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9117619 | |||||||
chr18:9117814 | C | G | 1 | a0001c0001t0001g0134 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.55-24C>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 1/7 | chr18 | 9117814 | |||||||
chr18:9118081 | C | A | 1 | a0001c0001t0001g0160 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.120+178C>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 2/7 | chr18 | 9118081 | |||||||
chr18:9118157 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.120+254A>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 2/7 | chr18 | 9118157 | |||||||
chr18:9118317 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.120+414G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 2/7 | chr18 | 9118317 | |||||||
chr18:9118521 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.120+618G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 2/7 | chr18 | 9118521 | |||||||
chr18:9118636 | C | T | 15 | a0001c0001t0001g0002 a0001c0001t0001g0048 a0001c0001t0001g0049 others(12): Show |
34 | HG00140.hp2 HG00639.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.121-690C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 2/7 | chr18 | 9118636 | |||||||
chr18:9118815 | G | GT | 49 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0032 others(46): Show |
86 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.121-486dupT | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 9118815 | ||||||
chr18:9118815 | G | GTT | 52 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(49): Show |
96 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.121-487_121-486dup others(2): Show |
NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 9118815 | ||||||
chr18:9118815 | G | GTTT | 37 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(34): Show |
63 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.121-488_121-486dup others(3): Show |
NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 9118815 | ||||||
chr18:9118815 | G | GTTTT | 7 | a0001c0001t0001g0024 a0001c0001t0001g0110 a0001c0001t0001g0116 others(4): Show |
9 | HG00280.hp2 HG01099.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.121-489_121-486dup others(4): Show |
NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 9118815 | ||||||
chr18:9118815 | GTTTTTTT others(3): Show |
G | 1 | a0001c0001t0001g0036 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.121-495_121-486del others(10): Show |
NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 9118815 | ||||||
chr18:9118962 | T | G | 1 | a0001c0001t0001g0124 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.121-364T>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 2/7 | chr18 | 9118962 | |||||||
chr18:9119037 | T | G | 97 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(94): Show |
167 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.121-289T>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 2/7 | chr18 | 9119037 | |||||||
chr18:9119158 | T | C | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(148): Show |
260 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.121-168T>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 2/7 | chr18 | 9119158 | |||||||
chr18:9119262 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.121-64T>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 2/7 | chr18 | 9119262 | |||||||
chr18:9119685 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.300+95G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 4/7 | chr18 | 9119685 | |||||||
chr18:9119765 | A | T | 1 | a0002c0002t0001g0062 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.300+175A>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 4/7 | chr18 | 9119765 | |||||||
chr18:9119821 | T | A | 1 | a0001c0001t0001g0190 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.300+231T>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 4/7 | chr18 | 9119821 | |||||||
chr18:9119822 | A | G | 1 | a0001c0001t0001g0030 | 2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.300+232A>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 4/7 | chr18 | 9119822 | |||||||
chr18:9119993 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.300+403T>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 4/7 | chr18 | 9119993 | |||||||
chr18:9120045 | A | G | 17 | a0001c0001t0001g0002 a0001c0001t0001g0048 a0001c0001t0001g0049 others(14): Show |
36 | HG00140.hp2 HG00639.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.300+455A>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 4/7 | chr18 | 9120045 | |||||||
chr18:9120063 | C | T | 16 | a0001c0001t0001g0002 a0001c0001t0001g0048 a0001c0001t0001g0049 others(13): Show |
35 | HG00140.hp2 HG00639.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.300+473C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 4/7 | chr18 | 9120063 | |||||||
chr18:9120267 | C | A | 124 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(121): Show |
207 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.300+677C>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 4/7 | chr18 | 9120267 | |||||||
chr18:9120301 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.300+711T>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 4/7 | chr18 | 9120301 | |||||||
chr18:9120423 | C | T | 1 | a0001c0001t0001g0174 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.300+833C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 4/7 | chr18 | 9120423 | |||||||
chr18:9120510 | A | C | 2 | a0001c0001t0001g0022 a0001c0001t0001g0100 |
4 | HG00673.hp2 HG02027.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.300+920A>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 4/7 | chr18 | 9120510 | |||||||
chr18:9120556 | C | G | 1 | a0001c0001t0001g0190 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.300+966C>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 4/7 | chr18 | 9120556 | |||||||
chr18:9120673 | G | GTAT | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(148): Show |
260 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.300+1084_300+1085i others(5): Show |
NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 9120673 | ||||||
chr18:9121224 | C | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0157 others(1): Show |
8 | HG01884.hp2 HG01891.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.301-1289C>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 4/7 | chr18 | 9121224 | |||||||
chr18:9121295 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.301-1218G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 4/7 | chr18 | 9121295 | |||||||
chr18:9121332 | A | T | 1 | a0001c0001t0001g0179 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.301-1181A>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 4/7 | chr18 | 9121332 | |||||||
chr18:9121377 | A | T | 2 | a0001c0001t0001g0160 a0001c0001t0001g0163 |
2 | HG02976.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.301-1136A>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 4/7 | chr18 | 9121377 | |||||||
chr18:9121413 | G | T | 1 | a0001c0001t0001g0160 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.301-1100G>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 4/7 | chr18 | 9121413 | |||||||
chr18:9121498 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | NA18949.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.301-1015G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 4/7 | chr18 | 9121498 | |||||||
chr18:9121501 | C | T | 1 | a0002c0002t0001g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.301-1012C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 4/7 | chr18 | 9121501 | |||||||
chr18:9121885 | A | T | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(103): Show |
180 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.301-628A>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 4/7 | chr18 | 9121885 | |||||||
chr18:9121937 | GTGAT | G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0165 |
6 | HG01243.hp2 HG02257.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.301-573_301-570del others(4): Show |
NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 9121937 | ||||||
chr18:9122115 | T | G | 1 | a0001c0001t0002g0079 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.301-398T>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 4/7 | chr18 | 9122115 | |||||||
chr18:9122183 | T | A | 1 | a0001c0001t0001g0080 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.301-330T>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 4/7 | chr18 | 9122183 | |||||||
chr18:9122271 | G | A | 1 | a0002c0002t0001g0156 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.301-242G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 4/7 | chr18 | 9122271 | |||||||
chr18:9122506 | AT | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0157 others(1): Show |
8 | HG01884.hp2 HG01891.hp2 HG02630.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.301-3delT | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 9122506 | ||||||
chr18:9122778 | T | C | 1 | a0001c0001t0002g0079 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.469+97T>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 5/7 | chr18 | 9122778 | |||||||
chr18:9122955 | GATTGTTT others(10): Show |
G | 2 | a0001c0001t0001g0046 a0001c0001t0001g0162 |
3 | HG02055.hp2 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.469+288_469+304del others(17): Show |
NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 9122955 | ||||||
chr18:9123432 | T | A | 2 | a0001c0001t0001g0048 a0001c0001t0001g0176 |
3 | HG02615.hp2 HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.469+751T>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 5/7 | chr18 | 9123432 | |||||||
chr18:9123436 | G | T | 1 | a0001c0001t0001g0112 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.469+755G>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 5/7 | chr18 | 9123436 | |||||||
chr18:9123494 | T | C | 16 | a0001c0003t0001g0009 a0001c0003t0001g0015 a0001c0003t0001g0018 others(13): Show |
25 | HG00140.hp1 HG00733.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.469+813T>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 5/7 | chr18 | 9123494 | |||||||
chr18:9123513 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.469+832G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 5/7 | chr18 | 9123513 | |||||||
chr18:9123582 | C | A | 2 | a0001c0001t0001g0022 a0001c0001t0001g0100 |
4 | HG00673.hp2 HG02027.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.469+901C>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 5/7 | chr18 | 9123582 | |||||||
chr18:9123634 | G | A | 16 | a0001c0003t0001g0009 a0001c0003t0001g0015 a0001c0003t0001g0018 others(13): Show |
25 | HG00140.hp1 HG00733.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.469+953G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 5/7 | chr18 | 9123634 | |||||||
chr18:9123810 | A | C | 1 | a0001c0001t0001g0131 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.470-1064A>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 5/7 | chr18 | 9123810 | |||||||
chr18:9123861 | T | C | 2 | a0001c0001t0001g0019 a0001c0001t0001g0096 |
4 | NA18942.hp2 NA18968.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.470-1013T>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 5/7 | chr18 | 9123861 | |||||||
chr18:9123862 | G | A | 16 | a0001c0003t0001g0009 a0001c0003t0001g0015 a0001c0003t0001g0018 others(13): Show |
25 | HG00140.hp1 HG00733.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.470-1012G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 5/7 | chr18 | 9123862 | |||||||
chr18:9123876 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.470-998C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 5/7 | chr18 | 9123876 | |||||||
chr18:9123889 | T | C | 1 | a0002c0002t0001g0027 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.470-985T>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 5/7 | chr18 | 9123889 | |||||||
chr18:9123947 | C | T | 16 | a0001c0003t0001g0009 a0001c0003t0001g0015 a0001c0003t0001g0018 others(13): Show |
25 | HG00140.hp1 HG00733.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.470-927C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 5/7 | chr18 | 9123947 | |||||||
chr18:9124183 | G | GT | 22 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(19): Show |
45 | HG00140.hp2 HG00639.hp2 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.470-681dupT | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 9124183 | ||||||
chr18:9124184 | T | G | 1 | a0001c0001t0002g0079 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.470-690T>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 5/7 | chr18 | 9124184 | |||||||
chr18:9124256 | GACTACTG others(12): Show |
G | 3 | a0002c0002t0001g0058 a0002c0002t0001g0060 a0002c0002t0001g0081 |
3 | HG02895.hp1 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.470-603_470-585del others(19): Show |
NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 9124256 | ||||||
chr18:9124364 | C | A | 18 | a0001c0001t0001g0002 a0001c0001t0001g0048 a0001c0001t0001g0049 others(15): Show |
37 | HG00140.hp2 HG00639.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.470-510C>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 5/7 | chr18 | 9124364 | |||||||
chr18:9124367 | C | T | 2 | a0001c0001t0001g0160 a0001c0001t0001g0163 |
2 | HG02976.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.470-507C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 5/7 | chr18 | 9124367 | |||||||
chr18:9124374 | C | T | 1 | a0002c0002t0001g0072 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.470-500C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 5/7 | chr18 | 9124374 | |||||||
chr18:9124403 | C | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0189 |
5 | HG01884.hp2 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.470-471C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 5/7 | chr18 | 9124403 | |||||||
chr18:9124447 | C | CT | 13 | a0001c0001t0001g0022 a0001c0001t0001g0093 a0001c0001t0001g0094 others(10): Show |
16 | HG00673.hp2 HG02027.hp1 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.470-409dupT | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 9124447 | ||||||
chr18:9124509 | C | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0157 others(1): Show |
8 | HG01884.hp2 HG01891.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.470-365C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 5/7 | chr18 | 9124509 | |||||||
chr18:9124517 | C | T | 3 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0165 |
6 | HG01243.hp2 HG02257.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.470-357C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 5/7 | chr18 | 9124517 | |||||||
chr18:9124518 | G | A | 1 | a0001c0001t0001g0023 | 3 | HG00639.hp1 HG02055.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.470-356G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 5/7 | chr18 | 9124518 | |||||||
chr18:9124555 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.470-319T>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 5/7 | chr18 | 9124555 | |||||||
chr18:9124639 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.470-235G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 5/7 | chr18 | 9124639 | |||||||
chr18:9124768 | G | T | 1 | a0001c0001t0001g0121 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.470-106G>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 5/7 | chr18 | 9124768 | |||||||
chr18:9124801 | CT | C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
177 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.470-59delT | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 9124801 | ||||||
chr18:9125289 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.579+306C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 6/7 | chr18 | 9125289 | |||||||
chr18:9125494 | G | C | 1 | a0001c0001t0001g0140 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.579+511G>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 6/7 | chr18 | 9125494 | |||||||
chr18:9125535 | G | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0165 |
6 | HG01243.hp2 HG02257.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.579+552G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 6/7 | chr18 | 9125535 | |||||||
chr18:9125539 | C | G | 16 | a0001c0003t0001g0009 a0001c0003t0001g0015 a0001c0003t0001g0018 others(13): Show |
25 | HG00140.hp1 HG00733.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.579+556C>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 6/7 | chr18 | 9125539 | |||||||
chr18:9125540 | TG | T | 16 | a0001c0003t0001g0009 a0001c0003t0001g0015 a0001c0003t0001g0018 others(13): Show |
25 | HG00140.hp1 HG00733.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.579+558delG | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 6/7 | chr18 | 9125540 | |||||||
chr18:9125617 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.579+634C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 6/7 | chr18 | 9125617 | |||||||
chr18:9125618 | G | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0119 |
2 | HG02559.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.579+635G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 6/7 | chr18 | 9125618 | |||||||
chr18:9125785 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.579+802C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 6/7 | chr18 | 9125785 | |||||||
chr18:9125848 | C | T | 16 | a0001c0003t0001g0009 a0001c0003t0001g0015 a0001c0003t0001g0018 others(13): Show |
25 | HG00140.hp1 HG00733.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.579+865C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 6/7 | chr18 | 9125848 | |||||||
chr18:9125853 | G | C | 16 | a0001c0003t0001g0009 a0001c0003t0001g0015 a0001c0003t0001g0018 others(13): Show |
25 | HG00140.hp1 HG00733.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.579+870G>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 6/7 | chr18 | 9125853 | |||||||
chr18:9126071 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.580-760C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 6/7 | chr18 | 9126071 | |||||||
chr18:9126185 | T | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0152 a0001c0001t0001g0154 |
7 | HG02027.hp2 HG02040.hp1 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.580-646T>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 6/7 | chr18 | 9126185 | |||||||
chr18:9126206 | G | A | 2 | a0002c0002t0001g0016 a0002c0002t0001g0062 |
4 | HG00738.hp1 HG01123.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.580-625G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 6/7 | chr18 | 9126206 | |||||||
chr18:9126305 | C | T | 4 | a0001c0001t0001g0040 a0001c0001t0001g0119 a0001c0001t0001g0120 others(1): Show |
5 | HG02109.hp1 HG02559.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.580-526C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 6/7 | chr18 | 9126305 | |||||||
chr18:9126819 | T | A | 8 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0080 others(5): Show |
10 | HG02055.hp2 HG02647.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.580-12T>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 6/7 | chr18 | 9126819 | |||||||
chr18:9127095 | C | T | 8 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0097 others(5): Show |
11 | HG00423.hp2 HG00621.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.656+188C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9127095 | |||||||
chr18:9127105 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.656+198A>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9127105 | |||||||
chr18:9127206 | T | A | 1 | a0002c0002t0001g0059 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.656+299T>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9127206 | |||||||
chr18:9127510 | C | G | 2 | a0002c0002t0001g0061 a0002c0002t0001g0078 |
2 | NA19006.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.656+603C>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9127510 | |||||||
chr18:9127638 | A | G | 1 | a0002c0002t0001g0066 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.656+731A>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9127638 | |||||||
chr18:9127694 | G | A | 1 | a0001c0001t0002g0079 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.656+787G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9127694 | |||||||
chr18:9127798 | T | C | 16 | a0001c0003t0001g0009 a0001c0003t0001g0015 a0001c0003t0001g0018 others(13): Show |
25 | HG00140.hp1 HG00733.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.656+891T>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9127798 | |||||||
chr18:9127851 | G | A | 1 | a0001c0001t0002g0079 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.656+944G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9127851 | |||||||
chr18:9127962 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.656+1055G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9127962 | |||||||
chr18:9128047 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.656+1140G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9128047 | |||||||
chr18:9128227 | T | G | 1 | a0002c0002t0001g0054 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.656+1320T>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9128227 | |||||||
chr18:9128325 | T | G | 3 | a0002c0002t0001g0011 a0002c0002t0001g0070 a0002c0002t0001g0073 |
6 | NA18939.hp2 NA18982.hp2 NA19003.hp1 others(3): Show |
intron_variant | MODIFIER | c.656+1418T>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9128325 | |||||||
chr18:9128455 | G | A | 16 | a0001c0003t0001g0009 a0001c0003t0001g0015 a0001c0003t0001g0018 others(13): Show |
25 | HG00140.hp1 HG00733.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.656+1548G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9128455 | |||||||
chr18:9128461 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.656+1554A>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9128461 | |||||||
chr18:9129085 | G | T | 1 | a0001c0001t0001g0162 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.656+2178G>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9129085 | |||||||
chr18:9129141 | A | G | 1 | a0001c0001t0001g0163 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.656+2234A>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9129141 | |||||||
chr18:9129188 | G | A | 1 | a0002c0002t0001g0070 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.656+2281G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9129188 | |||||||
chr18:9129298 | A | G | 1 | a0001c0001t0001g0103 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.656+2391A>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9129298 | |||||||
chr18:9129339 | C | T | 3 | a0001c0003t0001g0031 a0001c0003t0001g0085 a0001c0003t0001g0115 |
4 | HG00733.hp1 HG01255.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.656+2432C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9129339 | |||||||
chr18:9129763 | C | T | 2 | a0001c0001t0001g0030 a0001c0001t0001g0157 |
3 | HG01891.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.656+2856C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9129763 | |||||||
chr18:9129860 | G | A | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(141): Show |
249 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.656+2953G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9129860 | |||||||
chr18:9129981 | T | G | 2 | a0001c0001t0001g0044 a0001c0001t0001g0158 |
3 | HG02647.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.656+3074T>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9129981 | |||||||
chr18:9130016 | G | C | 1 | a0002c0002t0001g0065 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.656+3109G>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9130016 | |||||||
chr18:9130027 | A | G | 1 | a0001c0001t0001g0049 | 2 | HG00741.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.656+3120A>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9130027 | |||||||
chr18:9130377 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.656+3470A>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9130377 | |||||||
chr18:9130401 | C | A | 1 | a0001c0001t0002g0079 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.656+3494C>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9130401 | |||||||
chr18:9130450 | T | C | 18 | a0001c0001t0001g0002 a0001c0001t0001g0048 a0001c0001t0001g0049 others(15): Show |
37 | HG00140.hp2 HG00639.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.656+3543T>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9130450 | |||||||
chr18:9130648 | ATATAGT | A | 4 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0165 others(1): Show |
7 | HG01243.hp2 HG02257.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.657-3528_657-3523d others(8): Show |
NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr18 | 9130648 | ||||||
chr18:9130768 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.657-3418C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9130768 | |||||||
chr18:9130866 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.657-3320G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9130866 | |||||||
chr18:9130978 | G | A | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(119): Show |
205 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.657-3208G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9130978 | |||||||
chr18:9131009 | T | C | 10 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0046 others(7): Show |
15 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.657-3177T>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9131009 | |||||||
chr18:9131537 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.657-2649C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9131537 | |||||||
chr18:9131743 | T | C | 1 | a0002c0002t0001g0071 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.657-2443T>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9131743 | |||||||
chr18:9131753 | ATGAC | A | 3 | a0001c0001t0001g0033 a0001c0001t0001g0091 a0001c0001t0001g0102 |
4 | HG00733.hp2 HG01109.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.657-2428_657-2425d others(6): Show |
NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr18 | 9131753 | ||||||
chr18:9131766 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.657-2420C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9131766 | |||||||
chr18:9131848 | G | GT | 16 | a0001c0003t0001g0009 a0001c0003t0001g0015 a0001c0003t0001g0018 others(13): Show |
25 | HG00140.hp1 HG00733.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.657-2337dupT | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr18 | 9131848 | ||||||
chr18:9131864 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.657-2322A>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9131864 | |||||||
chr18:9132003 | TGTA | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0157 others(1): Show |
8 | HG01884.hp2 HG01891.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.657-2181_657-2179d others(5): Show |
NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr18 | 9132003 | ||||||
chr18:9132070 | T | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0157 others(1): Show |
8 | HG01884.hp2 HG01891.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.657-2116T>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9132070 | |||||||
chr18:9132177 | A | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0157 others(1): Show |
8 | HG01884.hp2 HG01891.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.657-2009A>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9132177 | |||||||
chr18:9132204 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.657-1982G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9132204 | |||||||
chr18:9132373 | A | C | 152 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(149): Show |
261 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.657-1813A>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9132373 | |||||||
chr18:9132711 | C | T | 3 | a0001c0003t0001g0184 a0001c0003t0001g0186 a0001c0003t0001g0187 |
3 | HG01070.hp2 HG02572.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.657-1475C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9132711 | |||||||
chr18:9132719 | A | C | 1 | a0001c0001t0001g0157 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.657-1467A>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9132719 | |||||||
chr18:9132752 | G | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0165 |
6 | HG01243.hp2 HG02257.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.657-1434G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9132752 | |||||||
chr18:9132791 | C | T | 2 | a0001c0001t0001g0040 a0001c0001t0001g0120 |
3 | HG02109.hp1 HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.657-1395C>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9132791 | |||||||
chr18:9132851 | G | T | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | NA18949.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.657-1335G>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9132851 | |||||||
chr18:9133037 | G | C | 1 | a0001c0001t0001g0098 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.657-1149G>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9133037 | |||||||
chr18:9133118 | C | G | 1 | a0001c0001t0001g0160 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.657-1068C>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9133118 | |||||||
chr18:9133185 | A | C | 17 | a0001c0001t0001g0002 a0001c0001t0001g0048 a0001c0001t0001g0049 others(14): Show |
36 | HG00140.hp2 HG00639.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.657-1001A>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9133185 | |||||||
chr18:9133493 | G | A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0135 |
2 | HG01496.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.657-693G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9133493 | |||||||
chr18:9133502 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.657-684A>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9133502 | |||||||
chr18:9133630 | C | G | 1 | a0002c0002t0001g0059 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.657-556C>G | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9133630 | |||||||
chr18:9133785 | G | T | 1 | a0001c0001t0001g0189 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.657-401G>T | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9133785 | |||||||
chr18:9133925 | G | A | 1 | a0001c0001t0001g0025 | 3 | HG01516.hp1 HG01517.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.657-261G>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9133925 | |||||||
chr18:9133945 | GA | G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0165 |
6 | HG01243.hp2 HG02257.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.657-239delA | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr18 | 9133945 | ||||||
chr18:9134021 | A | C | 1 | a0001c0001t0001g0123 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.657-165A>C | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9134021 | |||||||
chr18:9134073 | T | A | 1 | a0002c0002t0001g0059 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.657-113T>A | NDUFV2 | ENSG00000178127.13 | transcript | ENST00000318388.11 | protein_coding | 7/7 | chr18 | 9134073 |