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
123751 BAA10g13610 A10 14601942 G A missense_variant MODERATE c.47C>T|p.Pro16Leu S80
123752 BAA10g13620 A10 14602805 G A missense_variant MODERATE c.536C>T|p.Ser179Phe S273
123753 BAA10g13610 A10 14603219 C T upstream_gene_variant MODIFIER c.-1231G>A| S108
123754 BAA10g13610 A10 14603929 C T upstream_gene_variant MODIFIER c.-1941G>A| S271
123755 BAA10g13620 A10 14604183 C T synonymous_variant LOW c.39G>A|p.Gln13Gln S87
123756 BAA10g13610 A10 14605179 C T upstream_gene_variant MODIFIER c.-3191G>A| S197
123757 BAA10g13610 A10 14605483 G A upstream_gene_variant MODIFIER c.-3495C>T| S68
123758 BAA10g13620 A10 14607253 G A upstream_gene_variant MODIFIER c.-3032C>T| S286
123759 BAA10g13620 A10 14607480 G T upstream_gene_variant MODIFIER c.-3259C>A| S287
123760 BAA10g13620 A10 14608076 G A upstream_gene_variant MODIFIER c.-3855C>T| S221
123761 BAA10g13620 A10 14608213 C T upstream_gene_variant MODIFIER c.-3992G>A| S16
123762 BAA10g13620 A10 14608516 G A upstream_gene_variant MODIFIER c.-4295C>T| S34
123763 BAA10g13620 A10 14608547 G A upstream_gene_variant MODIFIER c.-4326C>T| S18
123764 BAA10g13620 A10 14608713 C T upstream_gene_variant MODIFIER c.-4492G>A| S281
123765 BAA10g13630 A10 14609439 G A upstream_gene_variant MODIFIER c.-2793C>T| S261
123766 BAA10g13630 A10 14609682 G A upstream_gene_variant MODIFIER c.-3036C>T| S205
123767 BAA10g13630 A10 14609985 G A upstream_gene_variant MODIFIER c.-3339C>T| S134
123768 BAA10g13630 A10 14610573 G A upstream_gene_variant MODIFIER c.-3927C>T| S64
123769 BAA10g13630 A10 14610939 G A upstream_gene_variant MODIFIER c.-4293C>T| S192
123770 BAA10g13630 A10 14611435 G A upstream_gene_variant MODIFIER c.-4789C>T| S280
123771 BAA10g13650 A10 14612733 C T upstream_gene_variant MODIFIER c.-2683C>T| S183
123772 BAA10g13650 A10 14613139 G A upstream_gene_variant MODIFIER c.-2277G>A| S198
123773 BAA10g13640 A10 14613659 G A missense_variant MODERATE c.1189G>A|p.Val397Ile S198
123774 BAA10g13650 A10 14614500 G A upstream_gene_variant MODIFIER c.-916G>A| S209
123775 BAA10g13650 A10 14616805 G A missense_variant MODERATE c.1390G>A|p.Val464Ile S257