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
117951 BAA10g10800 A10 12548802 G A upstream_gene_variant MODIFIER c.-4016G>A| S245
117952 BAA10g10800 A10 12548909 C T upstream_gene_variant MODIFIER c.-3909C>T| S146
117953 BAA10g10800 A10 12549017 G A upstream_gene_variant MODIFIER c.-3801G>A| S35
117954 BAA10g10790 A10 12549434 G A missense_variant MODERATE c.169C>T|p.Leu57Phe S18
117955 BAA10g10790 A10 12549682 C T upstream_gene_variant MODIFIER c.-80G>A| S144
117956 BAA10g10790 A10 12549683 C T upstream_gene_variant MODIFIER c.-81G>A| S164
117957 BAA10g10790 A10 12549883 G A upstream_gene_variant MODIFIER c.-281C>T| S217
117958 BAA10g10790 A10 12551509 C T upstream_gene_variant MODIFIER c.-1907G>A| S156
117959 BAA10g10790 A10 12552194 G A upstream_gene_variant MODIFIER c.-2592C>T| S200
117960 BAA10g10800 A10 12552924 G A missense_variant MODERATE c.107G>A|p.Gly36Asp S182
117961 BAA10g10790 A10 12553236 C T upstream_gene_variant MODIFIER c.-3634G>A| S260
117962 BAA10g10800 A10 12553741 G A splice_acceptor_variant&intron_variant HIGH c.463-1G>A| S261
117963 BAA10g10800 A10 12556629 C T downstream_gene_variant MODIFIER c.*2418C>T| S187
117964 BAA10g10810 A10 12559633 C T upstream_gene_variant MODIFIER c.-378G>A| S249
117965 BAA10g10810 A10 12560160 C T upstream_gene_variant MODIFIER c.-905G>A| S173
117966 BAA10g10810 A10 12561197 C T upstream_gene_variant MODIFIER c.-1942G>A| S20
117967 BAA10g10810 A10 12561201 G A upstream_gene_variant MODIFIER c.-1946C>T| S67
117968 BAA10g10810 A10 12561204 C T upstream_gene_variant MODIFIER c.-1949G>A| S149
117969 BAA10g10810 A10 12561622 G A upstream_gene_variant MODIFIER c.-2367C>T| S274
117970 BAA10g10810 A10 12562886 G A upstream_gene_variant MODIFIER c.-3631C>T| S216
117971 BAA10g10810 A10 12562906 C T upstream_gene_variant MODIFIER c.-3651G>A| S104
S52
117972 BAA10g10810 A10 12564216 C T upstream_gene_variant MODIFIER c.-4961G>A| S17
117973 BAA10g10810-BAA10g10820 A10 12564558 G A intergenic_region MODIFIER n.12564558G>A| S140
117974 BAA10g10810-BAA10g10820 A10 12568564 G A intergenic_region MODIFIER n.12568564G>A| S298
117975 BAA10g10810-BAA10g10820 A10 12569113 C T intergenic_region MODIFIER n.12569113C>T| S211