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
155751 BAA02g03830 A02 1687561 C T upstream_gene_variant MODIFIER c.-517C>T| S212
155752 BAA02g03830 A02 1687940 C T upstream_gene_variant MODIFIER c.-138C>T| S172
S217
155753 BAA02g03830 A02 1689299 G A missense_variant MODERATE c.790G>A|p.Asp264Asn S174
155754 BAA02g03850 A02 1690293 G A upstream_gene_variant MODIFIER c.-4478G>A| S166
155755 BAA02g03850 A02 1690334 C T upstream_gene_variant MODIFIER c.-4437C>T| S75
155756 BAA02g03830 A02 1690476 G A synonymous_variant LOW c.1563G>A|p.Leu521Leu S60
155757 BAA02g03830 A02 1691429 G A missense_variant MODERATE c.2434G>A|p.Asp812Asn S164
155758 BAA02g03850 A02 1691774 G A upstream_gene_variant MODIFIER c.-2997G>A| S168
155759 BAA02g03850 A02 1692373 G A upstream_gene_variant MODIFIER c.-2398G>A| S184
155760 BAA02g03840 A02 1693143 G A synonymous_variant LOW c.411C>T|p.Asn137Asn S140
155761 BAA02g03850 A02 1693353 G A upstream_gene_variant MODIFIER c.-1418G>A| S162
155762 BAA02g03840 A02 1693614 C T missense_variant MODERATE c.212G>A|p.Gly71Glu S61
155763 BAA02g03840 A02 1694330 C T upstream_gene_variant MODIFIER c.-365G>A| S255
155764 BAA02g03850 A02 1694887 C T synonymous_variant LOW c.117C>T|p.Phe39Phe S277
155765 BAA02g03850 A02 1695730 G A synonymous_variant LOW c.960G>A|p.Leu320Leu S35
155766 BAA02g03850 A02 1695781 G A synonymous_variant LOW c.1011G>A|p.Thr337Thr S215
155767 BAA02g03860 A02 1697376 C T missense_variant MODERATE c.571G>A|p.Gly191Arg S2
155768 BAA02g03860 A02 1697540 G A synonymous_variant LOW c.498C>T|p.Asp166Asp S221
155769 BAA02g03860 A02 1698430 C T missense_variant MODERATE c.197G>A|p.Gly66Glu S178
155770 BAA02g03870 A02 1700213 G A missense_variant MODERATE c.1094C>T|p.Pro365Leu S105
S106
155771 BAA02g03870 A02 1700297 C T missense_variant MODERATE c.1010G>A|p.Gly337Glu S240
155772 BAA02g03870 A02 1701010 C T synonymous_variant LOW c.363G>A|p.Glu121Glu S80
155773 BAA02g03870 A02 1701104 C T missense_variant MODERATE c.269G>A|p.Arg90Lys S112
155774 BAA02g03870 A02 1701160 C T synonymous_variant LOW c.213G>A|p.Ala71Ala S129
155775 BAA02g03870 A02 1701428 G A missense_variant MODERATE c.11C>T|p.Ala4Val S80