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
178901 BAA02g19640 A02 10211566 G A upstream_gene_variant MODIFIER c.-3287G>A| S134
178902 BAA02g19630 A02 10212302 C T missense_variant MODERATE c.934G>A|p.Gly312Arg S281
178903 BAA02g19630 A02 10212416 C T missense_variant MODERATE c.820G>A|p.Val274Ile S302
178904 BAA02g19630 A02 10213084 G A missense_variant MODERATE c.152C>T|p.Ser51Leu S245
178905 BAA02g19630 A02 10214259 G A upstream_gene_variant MODIFIER c.-1024C>T| S166
178906 BAA02g19630 A02 10214374 C T upstream_gene_variant MODIFIER c.-1139G>A| S224
178907 BAA02g19640 A02 10215167 G A synonymous_variant LOW c.315G>A|p.Lys105Lys S81
178908 BAA02g19640 A02 10215583 C T missense_variant MODERATE c.626C>T|p.Ala209Val S25
178909 BAA02g19640 A02 10217125 C T synonymous_variant LOW c.1803C>T|p.Ala601Ala S165
178910 BAA02g19640 A02 10217177 C T missense_variant MODERATE c.1855C>T|p.Pro619Ser S181
178911 BAA02g19630 A02 10217505 C T upstream_gene_variant MODIFIER c.-4270G>A| S28
178912 BAA02g19630 A02 10217822 G A upstream_gene_variant MODIFIER c.-4587C>T| S170
178913 BAA02g19660 A02 10220253 G A synonymous_variant LOW c.1266C>T|p.Asp422Asp S187
178914 BAA02g19660 A02 10220529 C T missense_variant MODERATE c.1068G>A|p.Met356Ile S165
178915 BAA02g19660 A02 10220555 C T missense_variant MODERATE c.1042G>A|p.Glu348Lys S46
178916 BAA02g19640 A02 10220916 C T downstream_gene_variant MODIFIER c.*2539C>T| S302
178917 BAA02g19660 A02 10222328 C T synonymous_variant LOW c.93G>A|p.Glu31Glu S284
178918 BAA02g19660 A02 10222478 G A upstream_gene_variant MODIFIER c.-58C>T| S303
178919 BAA02g19660 A02 10222698 G A upstream_gene_variant MODIFIER c.-278C>T| S136
178920 BAA02g19660 A02 10223055 G A upstream_gene_variant MODIFIER c.-635C>T| S148
S210
S30
S31
178921 BAA02g19660 A02 10223731 C T upstream_gene_variant MODIFIER c.-1311G>A| S289
S290
178922 BAA02g19660 A02 10224013 G A upstream_gene_variant MODIFIER c.-1593C>T| S174
S27
178923 BAA02g19660 A02 10224083 G A upstream_gene_variant MODIFIER c.-1663C>T| S202
178924 BAA02g19660 A02 10224869 C T upstream_gene_variant MODIFIER c.-2449G>A| S241
178925 BAA02g19660 A02 10225171 G A upstream_gene_variant MODIFIER c.-2751C>T| S247