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
99851 BAA10g06680 A10 3580039 C T downstream_gene_variant MODIFIER c.*4651C>T| S73
S91
99852 BAA10g06680 A10 3580114 G A downstream_gene_variant MODIFIER c.*4726G>A| S306
S308
99853 BAA10g06680 A10 3580243 C T downstream_gene_variant MODIFIER c.*4855C>T| S42
99854 BAA10g06680 A10 3580302 C T downstream_gene_variant MODIFIER c.*4914C>T| S204
99855 BAA10g06690 A10 3580744 C T downstream_gene_variant MODIFIER c.*367G>A| S37
99856 BAA10g06690 A10 3581362 G A missense_variant MODERATE c.1000C>T|p.His334Tyr S19
99857 BAA10g06690 A10 3581774 G A intron_variant MODIFIER c.846-258C>T| S134
99858 BAA10g06690 A10 3582256 C T intron_variant MODIFIER c.845+323G>A| S35
99859 BAA10g06690 A10 3582837 G A intron_variant MODIFIER c.721-134C>T| S182
99860 BAA10g06690 A10 3583348 G A intron_variant MODIFIER c.502-19C>T| S20
99861 BAA10g06690 A10 3583799 C T synonymous_variant LOW c.264G>A|p.Ser88Ser S247
99862 BAA10g06690 A10 3584047 C T missense_variant MODERATE c.16G>A|p.Val6Ile S294
99863 BAA10g06690 A10 3584564 C T upstream_gene_variant MODIFIER c.-502G>A| S263
99864 BAA10g06690 A10 3585522 G A upstream_gene_variant MODIFIER c.-1460C>T| S184
99865 BAA10g06690 A10 3586475 G A upstream_gene_variant MODIFIER c.-2413C>T| S245
99866 BAA10g06690 A10 3586675 G A upstream_gene_variant MODIFIER c.-2613C>T| S179
99867 BAA10g06700 A10 3589089 G A downstream_gene_variant MODIFIER c.*2511C>T| S164
99868 BAA10g06700 A10 3589099 G A downstream_gene_variant MODIFIER c.*2501C>T| S283
99869 BAA10g06700 A10 3589552 C T downstream_gene_variant MODIFIER c.*2048G>A| S247
99870 BAA10g06700 A10 3589567 T C downstream_gene_variant MODIFIER c.*2033A>G| S23
99871 BAA10g06700 A10 3589615 C T downstream_gene_variant MODIFIER c.*1985G>A| S8
99872 BAA10g06700 A10 3589744 G A downstream_gene_variant MODIFIER c.*1856C>T| S95
99873 BAA10g06700 A10 3590140 G A downstream_gene_variant MODIFIER c.*1460C>T| S268
99874 BAA10g06700 A10 3590341 C T downstream_gene_variant MODIFIER c.*1259G>A| S8
99875 BAA10g06700 A10 3590772 C T downstream_gene_variant MODIFIER c.*828G>A| S197