Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 489298 of 489298 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
132751 BAA10g19520 A10 17876761 C T missense_variant MODERATE c.208G>A|p.Glu70Lys S127
132752 BAA10g19520 A10 17877012 G A missense_variant MODERATE c.35C>T|p.Ala12Val S112
132753 BAA10g19520 A10 17877343 G T upstream_gene_variant MODIFIER c.-56C>A| S236
132754 BAA10g19520 A10 17877467 C T upstream_gene_variant MODIFIER c.-180G>A| S172
S247
132755 BAA10g19520 A10 17878290 G A upstream_gene_variant MODIFIER c.-1003C>T| S273
132756 BAA10g19520 A10 17880462 C T upstream_gene_variant MODIFIER c.-3175G>A| S183
132757 BAA10g19530 A10 17880994 C T missense_variant MODERATE c.1034G>A|p.Arg345Lys S305
132758 BAA10g19520 A10 17881549 G A upstream_gene_variant MODIFIER c.-4262C>T| S139
132759 BAA10g19530 A10 17882141 C T missense_variant MODERATE c.695G>A|p.Arg232Lys S67
132760 BAA10g19530 A10 17882371 G A synonymous_variant LOW c.465C>T|p.Tyr155Tyr S61
132761 BAA10g19530 A10 17882584 G A synonymous_variant LOW c.252C>T|p.Ser84Ser S65
132762 BAA10g19530 A10 17883185 G A upstream_gene_variant MODIFIER c.-350C>T| S184
132763 BAA10g19530 A10 17884228 G A upstream_gene_variant MODIFIER c.-1393C>T| S178
132764 BAA10g19530 A10 17886408 C T upstream_gene_variant MODIFIER c.-3573G>A| S37
132765 BAA10g19530 A10 17886645 G A upstream_gene_variant MODIFIER c.-3810C>T| S71
132766 BAA10g19530 A10 17886974 G A upstream_gene_variant MODIFIER c.-4139C>T| S255
132767 BAA10g19540 A10 17892068 C T downstream_gene_variant MODIFIER c.*3795G>A| S25
132768 BAA10g19540 A10 17892305 G A downstream_gene_variant MODIFIER c.*3558C>T| S217
132769 BAA10g19540 A10 17892640 C T downstream_gene_variant MODIFIER c.*3223G>A| S302
132770 BAA10g19540 A10 17892669 C T downstream_gene_variant MODIFIER c.*3194G>A| S113
132771 BAA10g19540 A10 17893097 C T downstream_gene_variant MODIFIER c.*2766G>A| S68
132772 BAA10g19540 A10 17894250 G A downstream_gene_variant MODIFIER c.*1613C>T| S180
132773 BAA10g19540 A10 17896055 C T synonymous_variant LOW c.549G>A|p.Pro183Pro S244
132774 BAA10g19540 A10 17896334 G A synonymous_variant LOW c.361C>T|p.Leu121Leu S178
132775 BAA10g19550 A10 17896627 C T downstream_gene_variant MODIFIER c.*883G>A| S148
S210
S30
S31