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
85651 BAA01g45400 A01 30298271 C T upstream_gene_variant MODIFIER c.-3724G>A| S92
85652 BAA01g45400 A01 30298910 G A upstream_gene_variant MODIFIER c.-4363C>T| S243
S299
85653 BAA01g45400 A01 30299094 G A upstream_gene_variant MODIFIER c.-4547C>T| S302
85654 BAA01g45430 A01 30300275 G A synonymous_variant LOW c.138C>T|p.Asp46Asp S158
85655 BAA01g45430 A01 30300394 C T missense_variant MODERATE c.19G>A|p.Glu7Lys S277
85656 BAA01g45430 A01 30300455 G A upstream_gene_variant MODIFIER c.-43C>T| S36
85657 BAA01g45430 A01 30301631 C T upstream_gene_variant MODIFIER c.-1219G>A| S303
85658 BAA01g45440 A01 30301994 G A synonymous_variant LOW c.231G>A|p.Lys77Lys S122
85659 BAA01g45440 A01 30301997 G A synonymous_variant LOW c.234G>A|p.Arg78Arg S262
85660 BAA01g45440 A01 30302029 C T missense_variant MODERATE c.266C>T|p.Pro89Leu S231
85661 BAA01g45430 A01 30302363 C T upstream_gene_variant MODIFIER c.-1951G>A| S204
85662 BAA01g45440 A01 30302783 G A missense_variant MODERATE c.562G>A|p.Gly188Arg S129
85663 BAA01g45440 A01 30303010 C T synonymous_variant LOW c.621C>T|p.Ile207Ile S42
85664 BAA01g45440 A01 30303431 C T missense_variant MODERATE c.928C>T|p.His310Tyr S8
85665 BAA01g45440 A01 30303461 G A missense_variant MODERATE c.958G>A|p.Gly320Arg S293
85666 BAA01g45430 A01 30304221 C T upstream_gene_variant MODIFIER c.-3809G>A| S127
85667 BAA01g45450 A01 30305173 C T stop_gained HIGH c.322C>T|p.Gln108* S153
S213
85668 BAA01g45450 A01 30305472 C T synonymous_variant LOW c.621C>T|p.Val207Val S12
85669 BAA01g45450 A01 30305602 G A missense_variant MODERATE c.751G>A|p.Ala251Thr S70
85670 BAA01g45450 A01 30306241 G A missense_variant MODERATE c.1390G>A|p.Gly464Arg S161
85671 BAA01g45450 A01 30307319 C T missense_variant MODERATE c.1897C>T|p.Pro633Ser S201
85672 BAA01g45440 A01 30308151 C T downstream_gene_variant MODIFIER c.*4365C>T| S37
85673 BAA01g45440 A01 30308525 C T downstream_gene_variant MODIFIER c.*4739C>T| S274
85674 BAA01g45450 A01 30308856 C T downstream_gene_variant MODIFIER c.*1133C>T| S81
S85
85675 BAA01g45450 A01 30310595 C T downstream_gene_variant MODIFIER c.*2872C>T| S157