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
99601 BAA10g06610-BAA10g06620 A10 3460624 G A intergenic_region MODIFIER n.3460624G>A| S289
99602 BAA10g06610-BAA10g06620 A10 3460687 G A intergenic_region MODIFIER n.3460687G>A| S150
99603 BAA10g06610-BAA10g06620 A10 3462116 G A intergenic_region MODIFIER n.3462116G>A| S273
99604 BAA10g06610-BAA10g06620 A10 3462360 C T intergenic_region MODIFIER n.3462360C>T| S47
99605 BAA10g06610-BAA10g06620 A10 3463151 C T intergenic_region MODIFIER n.3463151C>T| S155
S211
99606 BAA10g06610-BAA10g06620 A10 3464447 C T intergenic_region MODIFIER n.3464447C>T| S146
99607 BAA10g06610-BAA10g06620 A10 3464846 C T intergenic_region MODIFIER n.3464846C>T| S143
99608 BAA10g06610-BAA10g06620 A10 3465133 A C intergenic_region MODIFIER n.3465133A>C| S8
99609 BAA10g06610-BAA10g06620 A10 3465241 C T intergenic_region MODIFIER n.3465241C>T| S73
99610 BAA10g06610-BAA10g06620 A10 3465580 G A intergenic_region MODIFIER n.3465580G>A| S86
99611 BAA10g06610-BAA10g06620 A10 3466093 C T intergenic_region MODIFIER n.3466093C>T| S116
99612 BAA10g06610-BAA10g06620 A10 3466373 C T intergenic_region MODIFIER n.3466373C>T| S247
99613 BAA10g06610-BAA10g06620 A10 3467139 G A intergenic_region MODIFIER n.3467139G>A| S283
99614 BAA10g06610-BAA10g06620 A10 3467215 C T intergenic_region MODIFIER n.3467215C>T| S231
99615 BAA10g06620 A10 3469878 G A downstream_gene_variant MODIFIER c.*2904C>T| S125
99616 BAA10g06620 A10 3472085 C T downstream_gene_variant MODIFIER c.*697G>A| S84
S93
99617 BAA10g06620 A10 3472464 C T downstream_gene_variant MODIFIER c.*318G>A| S199
99618 BAA10g06620 A10 3473676 G A intron_variant MODIFIER c.2214-23C>T| S136
99619 BAA10g06620 A10 3474178 T A splice_region_variant&intron_variant LOW c.2034-4A>T| S176
99620 BAA10g06620 A10 3476805 C T synonymous_variant LOW c.771G>A|p.Leu257Leu S92
99621 BAA10g06620 A10 3476821 G A intron_variant MODIFIER c.766-11C>T| S268
99622 BAA10g06620 A10 3477013 C T synonymous_variant LOW c.675G>A|p.Glu225Glu S44
99623 BAA10g06620 A10 3477272 G A intron_variant MODIFIER c.647+113C>T| S90
99624 BAA10g06620 A10 3477697 C T splice_region_variant&intron_variant LOW c.498+6G>A| S259
99625 BAA10g06620 A10 3478396 C T synonymous_variant LOW c.195G>A|p.Arg65Arg S71