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
99551 BAA10g06570 A10 3430964 C T upstream_gene_variant MODIFIER c.-1193G>A| S67
99552 BAA10g06570 A10 3431117 C T upstream_gene_variant MODIFIER c.-1346G>A| S275
99553 BAA10g06580 A10 3431938 G A missense_variant MODERATE c.263C>T|p.Ala88Val S18
S216
99554 BAA10g06570 A10 3433378 G A upstream_gene_variant MODIFIER c.-3607C>T| S274
99555 BAA10g06570 A10 3433873 C T upstream_gene_variant MODIFIER c.-4102G>A| S54
99556 BAA10g06570 A10 3433932 C T upstream_gene_variant MODIFIER c.-4161G>A| S199
99557 BAA10g06590 A10 3434224 C T missense_variant MODERATE c.361C>T|p.Pro121Ser S194
99558 BAA10g06580 A10 3436382 G A upstream_gene_variant MODIFIER c.-3984C>T| S136
99559 BAA10g06590 A10 3437408 C T downstream_gene_variant MODIFIER c.*2777C>T| S124
99560 BAA10g06590 A10 3437696 G A downstream_gene_variant MODIFIER c.*3065G>A| S187
99561 BAA10g06590 A10 3438028 C T downstream_gene_variant MODIFIER c.*3397C>T| S174
S27
99562 BAA10g06590 A10 3438152 G A downstream_gene_variant MODIFIER c.*3521G>A| S17
99563 BAA10g06600 A10 3439158 C T upstream_gene_variant MODIFIER c.-4377C>T| S188
99564 BAA10g06600 A10 3440967 G A upstream_gene_variant MODIFIER c.-2568G>A| S109
99565 BAA10g06600 A10 3447201 G A downstream_gene_variant MODIFIER c.*3319G>A| S57
99566 BAA10g06600 A10 3447829 G A downstream_gene_variant MODIFIER c.*3947G>A| S203
99567 BAA10g06610 A10 3449020 G A downstream_gene_variant MODIFIER c.*3946C>T| S66
99568 BAA10g06610 A10 3449161 C T downstream_gene_variant MODIFIER c.*3805G>A| S130
99569 BAA10g06610 A10 3449472 G A downstream_gene_variant MODIFIER c.*3494C>T| S203
99570 BAA10g06610 A10 3452047 G A downstream_gene_variant MODIFIER c.*919C>T| S295
99571 BAA10g06610 A10 3452990 C T stop_gained HIGH c.1068G>A|p.Trp356* S289
99572 BAA10g06610 A10 3453511 G A missense_variant MODERATE c.547C>T|p.His183Tyr S209
99573 BAA10g06610 A10 3453765 G A missense_variant MODERATE c.293C>T|p.Ser98Leu S207
99574 BAA10g06610 A10 3453922 C T missense_variant MODERATE c.136G>A|p.Asp46Asn S225
S294
S73
99575 BAA10g06610-BAA10g06620 A10 3459700 C T intergenic_region MODIFIER n.3459700C>T| S238