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
31851 BAA01g22030 A01 10986062 G A upstream_gene_variant MODIFIER c.-510G>A| S293
31852 BAA01g22030 A01 10986447 C T upstream_gene_variant MODIFIER c.-125C>T| S267
31853 BAA01g22030 A01 10986654 C T missense_variant MODERATE c.83C>T|p.Ser28Phe S69
31854 BAA01g22030 A01 10987431 C T intron_variant MODIFIER c.492+20C>T| S134
31855 BAA01g22030 A01 10987535 G A intron_variant MODIFIER c.492+124G>A| S49
31856 BAA01g22030 A01 10988084 C T missense_variant MODERATE c.665C>T|p.Ala222Val S219
S72
31857 BAA01g22030 A01 10988278 C T synonymous_variant LOW c.859C>T|p.Leu287Leu S295
31858 BAA01g22040 A01 10988587 G A upstream_gene_variant MODIFIER c.-4511G>A| S178
S236
31859 BAA01g22040 A01 10990400 C T upstream_gene_variant MODIFIER c.-2698C>T| S303
31860 BAA01g22040 A01 10991915 C T upstream_gene_variant MODIFIER c.-1183C>T| S286
31861 BAA01g22040 A01 10993083 G A upstream_gene_variant MODIFIER c.-15G>A| S225
31862 BAA01g22040 A01 10993475 C T synonymous_variant LOW c.378C>T|p.Phe126Phe S25
31863 BAA01g22040 A01 10993548 G T missense_variant MODERATE c.451G>T|p.Gly151Cys S169
31864 BAA01g22040 A01 10994312 G A downstream_gene_variant MODIFIER c.*228G>A| S284
31865 BAA01g22060 A01 10995425 G A upstream_gene_variant MODIFIER c.-3907G>A| S251
31866 BAA01g22050 A01 10997607 G A missense_variant MODERATE c.653C>T|p.Thr218Ile S100
31867 BAA01g22060 A01 10997708 C T upstream_gene_variant MODIFIER c.-1624C>T| S255
31868 BAA01g22060 A01 10997864 G A upstream_gene_variant MODIFIER c.-1468G>A| S155
31869 BAA01g22060 A01 10997992 G A upstream_gene_variant MODIFIER c.-1340G>A| S178
31870 BAA01g22050 A01 10998756 G A stop_gained HIGH c.256C>T|p.Gln86* S239
31871 BAA01g22050 A01 10998943 C T synonymous_variant LOW c.69G>A|p.Val23Val S266
31872 BAA01g22060 A01 10999820 G A missense_variant MODERATE c.269G>A|p.Gly90Glu S294
31873 BAA01g22060 A01 10999852 C T missense_variant MODERATE c.301C>T|p.His101Tyr S277
31874 BAA01g22060 A01 10999861 G A missense_variant MODERATE c.310G>A|p.Glu104Lys S292
31875 BAA01g22050 A01 11000345 C T upstream_gene_variant MODIFIER c.-1334G>A| S277