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
180701 BAA02g20460 A02 10863599 G A upstream_gene_variant MODIFIER c.-4124C>T| S148
180702 BAA02g20460 A02 10864125 C T upstream_gene_variant MODIFIER c.-4650G>A| S270
180703 BAA02g20470 A02 10865217 C T upstream_gene_variant MODIFIER c.-1680C>T| S275
180704 BAA02g20470 A02 10866474 G A upstream_gene_variant MODIFIER c.-423G>A| S10
180705 BAA02g20470 A02 10866483 C T upstream_gene_variant MODIFIER c.-414C>T| S182
180706 BAA02g20480 A02 10867543 G A upstream_gene_variant MODIFIER c.-3366G>A| S297
180707 BAA02g20480 A02 10867894 C T upstream_gene_variant MODIFIER c.-3015C>T| S292
180708 BAA02g20480 A02 10870156 G A upstream_gene_variant MODIFIER c.-753G>A| S170
180709 BAA02g20480 A02 10870573 C T upstream_gene_variant MODIFIER c.-336C>T| S266
180710 BAA02g20490 A02 10871101 C T upstream_gene_variant MODIFIER c.-3859C>T| S53
180711 BAA02g20490 A02 10873438 G A upstream_gene_variant MODIFIER c.-1522G>A| S149
180712 BAA02g20490 A02 10874803 C T upstream_gene_variant MODIFIER c.-157C>T| S8
180713 BAA02g20490 A02 10874975 G A missense_variant MODERATE c.16G>A|p.Val6Ile S136
180714 BAA02g20490 A02 10875005 G A missense_variant MODERATE c.46G>A|p.Gly16Arg S284
S295
180715 BAA02g20490 A02 10875969 G A synonymous_variant LOW c.501G>A|p.Lys167Lys S79
S91
180716 BAA02g20480 A02 10876112 G A downstream_gene_variant MODIFIER c.*3231G>A| S263
180717 BAA02g20490 A02 10876652 G A synonymous_variant LOW c.663G>A|p.Pro221Pro S150
180718 BAA02g20490 A02 10877787 G A missense_variant MODERATE c.1081G>A|p.Ala361Thr S72
180719 BAA02g20490 A02 10878120 G A synonymous_variant LOW c.1341G>A|p.Arg447Arg S136
180720 BAA02g20500 A02 10878751 G A downstream_gene_variant MODIFIER c.*2377C>T| S41
180721 BAA02g20490 A02 10879372 C T downstream_gene_variant MODIFIER c.*169C>T| S118
180722 BAA02g20500 A02 10881323 C T synonymous_variant LOW c.1353G>A|p.Ser451Ser S193
180723 BAA02g20500 A02 10881356 G A synonymous_variant LOW c.1320C>T|p.Phe440Phe S166
180724 BAA02g20500 A02 10881683 C T stop_gained HIGH c.993G>A|p.Trp331* S25
180725 BAA02g20500 A02 10881823 C T missense_variant MODERATE c.853G>A|p.Glu285Lys S249