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
134701 BAA10g20840 A10 18557570 G A synonymous_variant LOW c.477G>A|p.Glu159Glu S62
134702 BAA10g20840 A10 18557919 C T downstream_gene_variant MODIFIER c.*184C>T| S121
134703 BAA10g20840 A10 18558000 C T downstream_gene_variant MODIFIER c.*265C>T| S157
S163
134704 BAA10g20840 A10 18558392 C T downstream_gene_variant MODIFIER c.*657C>T| S244
134705 BAA10g20840 A10 18558398 G A downstream_gene_variant MODIFIER c.*663G>A| S288
134706 BAA10g20850 A10 18558886 C T missense_variant MODERATE c.1196G>A|p.Gly399Asp S125
134707 BAA10g20850 A10 18559048 C T missense_variant MODERATE c.1034G>A|p.Arg345Lys S25
134708 BAA10g20840 A10 18559162 G A downstream_gene_variant MODIFIER c.*1427G>A| S192
134709 BAA10g20850 A10 18559458 G A missense_variant MODERATE c.790C>T|p.Leu264Phe S67
134710 BAA10g20850 A10 18559604 G A missense_variant MODERATE c.644C>T|p.Ala215Val S25
134711 BAA10g20850 A10 18560618 C T upstream_gene_variant MODIFIER c.-40G>A| S8
134712 BAA10g20850 A10 18560890 G A upstream_gene_variant MODIFIER c.-312C>T| S286
134713 BAA10g20850 A10 18561492 C T upstream_gene_variant MODIFIER c.-914G>A| S152
134714 BAA10g20850 A10 18562457 G A upstream_gene_variant MODIFIER c.-1879C>T| S158
134715 BAA10g20850 A10 18563222 G A upstream_gene_variant MODIFIER c.-2644C>T| S198
134716 BAA10g20850 A10 18564007 C T upstream_gene_variant MODIFIER c.-3429G>A| S114
134717 BAA10g20860 A10 18564246 G A missense_variant MODERATE c.2132C>T|p.Pro711Leu S1
S90
134718 BAA10g20850 A10 18564547 C T upstream_gene_variant MODIFIER c.-3969G>A| S56
134719 BAA10g20860 A10 18564895 C T synonymous_variant LOW c.1794G>A|p.Arg598Arg S168
S219
S72
134720 BAA10g20860 A10 18564951 C T missense_variant MODERATE c.1738G>A|p.Gly580Arg S96
134721 BAA10g20850 A10 18565013 G A upstream_gene_variant MODIFIER c.-4435C>T| S190
S286
S287
134722 BAA10g20860 A10 18565694 G A missense_variant MODERATE c.1403C>T|p.Thr468Ile S165
134723 BAA10g20860 A10 18567013 C T missense_variant MODERATE c.925G>A|p.Val309Ile S283
134724 BAA10g20860 A10 18567227 C T synonymous_variant LOW c.828G>A|p.Lys276Lys S308
134725 BAA10g20860 A10 18567537 C T intron_variant MODIFIER c.808+110G>A| S185