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
175701 BAA02g17950 A02 9021253 G A upstream_gene_variant MODIFIER c.-3302C>T| S129
175702 BAA02g17950 A02 9021843 C T upstream_gene_variant MODIFIER c.-3892G>A| S278
175703 BAA02g17960 A02 9022978 C T missense_variant MODERATE c.335C>T|p.Ser112Phe S32
175704 BAA02g17970 A02 9024034 C T downstream_gene_variant MODIFIER c.*2943G>A| S241
175705 BAA02g17960 A02 9024466 G A stop_gained HIGH c.962G>A|p.Trp321* S51
175706 BAA02g17960 A02 9024919 G A missense_variant MODERATE c.1340G>A|p.Gly447Glu S159
S243
175707 BAA02g17960 A02 9025039 C T missense_variant MODERATE c.1460C>T|p.Thr487Ile S160
175708 BAA02g17960 A02 9025422 G A downstream_gene_variant MODIFIER c.*349G>A| S238
175709 BAA02g17960 A02 9025599 C T downstream_gene_variant MODIFIER c.*526C>T| S244
175710 BAA02g17960 A02 9025941 C T downstream_gene_variant MODIFIER c.*868C>T| S131
175711 BAA02g17980 A02 9026914 G A upstream_gene_variant MODIFIER c.-4424G>A| S172
S217
175712 BAA02g17970 A02 9027813 C T missense_variant MODERATE c.1003G>A|p.Glu335Lys S138
175713 BAA02g17970 A02 9028066 C T synonymous_variant LOW c.750G>A|p.Ala250Ala S112
175714 BAA02g17970 A02 9028593 G A missense_variant MODERATE c.223C>T|p.Pro75Ser S169
175715 BAA02g17970 A02 9028996 C T missense_variant MODERATE c.4G>A|p.Asp2Asn S71
175716 BAA02g17970 A02 9029316 G A upstream_gene_variant MODIFIER c.-317C>T| S109
175717 BAA02g17970 A02 9031327 C T upstream_gene_variant MODIFIER c.-2328G>A| S66
175718 BAA02g17980 A02 9031691 C T synonymous_variant LOW c.195C>T|p.Asn65Asn S209
175719 BAA02g17980 A02 9031847 C T missense_variant MODERATE c.262C>T|p.Leu88Phe S73
S91
175720 BAA02g17980 A02 9031869 G A missense_variant MODERATE c.284G>A|p.Arg95Gln S132
S215
175721 BAA02g17970 A02 9032165 C T upstream_gene_variant MODIFIER c.-3166G>A| S292
175722 BAA02g17980 A02 9035152 C T downstream_gene_variant MODIFIER c.*3069C>T| S207
175723 BAA02g17990 A02 9037408 C T upstream_gene_variant MODIFIER c.-888G>A| S135
175724 BAA02g17990 A02 9037653 C T upstream_gene_variant MODIFIER c.-1133G>A| S163
175725 BAA02g17990 A02 9037665 C T upstream_gene_variant MODIFIER c.-1145G>A| S202