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
141601 BAA10g26590 A10 21039954 C T downstream_gene_variant MODIFIER c.*1052C>T| S48
141602 BAA10g26590 A10 21040489 C T downstream_gene_variant MODIFIER c.*1587C>T| S210
141603 BAA10g26610 A10 21041803 C A synonymous_variant LOW c.2679G>T|p.Leu893Leu S288
141604 BAA10g26610 A10 21041811 C T missense_variant MODERATE c.2671G>A|p.Val891Ile S13
141605 BAA10g26610 A10 21042560 C T missense_variant MODERATE c.2039G>A|p.Gly680Glu S209
141606 BAA10g26610 A10 21042690 C A missense_variant MODERATE c.1909G>T|p.Ala637Ser S12
S260
S91
141607 BAA10g26610 A10 21043739 G A missense_variant MODERATE c.860C>T|p.Ser287Leu S71
141608 BAA10g26610 A10 21044007 C T missense_variant MODERATE c.592G>A|p.Glu198Lys S96
141609 BAA10g26600 A10 21045055 G A downstream_gene_variant MODIFIER c.*4334G>A| S288
141610 BAA10g26610 A10 21046834 T G upstream_gene_variant MODIFIER c.-1620A>C| S148
S236
141611 BAA10g26610 A10 21046914 C T upstream_gene_variant MODIFIER c.-1700G>A| S210
141612 BAA10g26620 A10 21052652 C T upstream_gene_variant MODIFIER c.-2683G>A| S14
141613 BAA10g26620 A10 21052710 C T upstream_gene_variant MODIFIER c.-2741G>A| S25
141614 BAA10g26620 A10 21052843 G A upstream_gene_variant MODIFIER c.-2874C>T| S88
141615 BAA10g26630 A10 21055224 G A upstream_gene_variant MODIFIER c.-692G>A| S263
141616 BAA10g26630 A10 21055349 C T upstream_gene_variant MODIFIER c.-567C>T| S168
141617 BAA10g26630 A10 21055428 G A upstream_gene_variant MODIFIER c.-488G>A| S256
141618 BAA10g26630 A10 21055575 C T upstream_gene_variant MODIFIER c.-341C>T| S68
141619 BAA10g26630 A10 21055935 C T missense_variant MODERATE c.20C>T|p.Ala7Val S25
141620 BAA10g26630 A10 21056526 G A stop_gained HIGH c.611G>A|p.Trp204* S112
141621 BAA10g26630 A10 21056624 C T stop_gained HIGH c.709C>T|p.Gln237* S5
141622 BAA10g26630 A10 21057130 C T missense_variant MODERATE c.881C>T|p.Ala294Val S168
141623 BAA10g26630 A10 21057138 G A missense_variant MODERATE c.889G>A|p.Ala297Thr S50
141624 BAA10g26650 A10 21059906 C T upstream_gene_variant MODIFIER c.-2123C>T| S33
141625 BAA10g26650 A10 21060335 G A upstream_gene_variant MODIFIER c.-1694G>A| S69