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
71851 BAA01g37610 A01 25119873 C T upstream_gene_variant MODIFIER c.-3716C>T| S68
71852 BAA01g37610 A01 25120874 C T upstream_gene_variant MODIFIER c.-2715C>T| S32
71853 BAA01g37610 A01 25123900 G A missense_variant MODERATE c.232G>A|p.Gly78Arg S135
71854 BAA01g37610 A01 25125626 G A missense_variant MODERATE c.1517G>A|p.Gly506Glu S13
71855 BAA01g37610 A01 25125642 G A synonymous_variant LOW c.1533G>A|p.Pro511Pro S20
71856 BAA01g37610 A01 25125738 G A synonymous_variant LOW c.1629G>A|p.Thr543Thr S117
71857 BAA01g37610 A01 25125795 G A stop_gained HIGH c.1686G>A|p.Trp562* S129
71858 BAA01g37610 A01 25125900 C T synonymous_variant LOW c.1791C>T|p.Leu597Leu S16
71859 BAA01g37620 A01 25130255 C T upstream_gene_variant MODIFIER c.-1499C>T| S298
71860 BAA01g37620 A01 25130493 C T upstream_gene_variant MODIFIER c.-1261C>T| S179
71861 BAA01g37620 A01 25130692 G A upstream_gene_variant MODIFIER c.-1062G>A| S45
71862 BAA01g37620 A01 25130717 G A upstream_gene_variant MODIFIER c.-1037G>A| S185
71863 BAA01g37620 A01 25130745 C T upstream_gene_variant MODIFIER c.-1009C>T| S144
71864 BAA01g37620 A01 25130936 C T upstream_gene_variant MODIFIER c.-818C>T| S180
71865 BAA01g37620 A01 25131300 C T upstream_gene_variant MODIFIER c.-454C>T| S115
71866 BAA01g37620 A01 25131742 G A upstream_gene_variant MODIFIER c.-12G>A| S83
S88
71867 BAA01g37620 A01 25131760 G A missense_variant MODERATE c.7G>A|p.Gly3Ser S223
71868 BAA01g37620 A01 25131851 G A missense_variant MODERATE c.98G>A|p.Arg33Lys S144
71869 BAA01g37620 A01 25132193 G A synonymous_variant LOW c.297G>A|p.Ser99Ser S96
71870 BAA01g37620 A01 25132437 G A intron_variant MODIFIER c.373+168G>A| S45
71871 BAA01g37620 A01 25132936 G A intron_variant MODIFIER c.373+667G>A| S257
71872 BAA01g37620 A01 25133663 G A intron_variant MODIFIER c.374-120G>A| S292
71873 BAA01g37620 A01 25133708 G A intron_variant MODIFIER c.374-75G>A| S212
71874 BAA01g37620 A01 25133869 G A missense_variant MODERATE c.460G>A|p.Asp154Asn S143
71875 BAA01g37620 A01 25134379 C T stop_gained HIGH c.757C>T|p.Gln253* S51