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
141751 BAA10g26770 A10 21096457 G A missense_variant MODERATE c.2467G>A|p.Val823Met S278
141752 BAA10g26780 A10 21096513 C T upstream_gene_variant MODIFIER c.-1311C>T| S257
141753 BAA10g26780 A10 21097492 C T upstream_gene_variant MODIFIER c.-332C>T| S140
141754 BAA10g26780 A10 21098205 G A missense_variant MODERATE c.280G>A|p.Asp94Asn S4
141755 BAA10g26770 A10 21098655 C T downstream_gene_variant MODIFIER c.*2166C>T| S140
141756 BAA10g26770 A10 21099145 G A downstream_gene_variant MODIFIER c.*2656G>A| S57
141757 BAA10g26790 A10 21101342 C T synonymous_variant LOW c.114G>A|p.Glu38Glu S18
141758 BAA10g26790 A10 21101754 C T upstream_gene_variant MODIFIER c.-299G>A| S302
141759 BAA10g26800 A10 21104534 C T missense_variant MODERATE c.89C>T|p.Ser30Phe S115
141760 BAA10g26800 A10 21104913 G A synonymous_variant LOW c.468G>A|p.Gly156Gly S216
141761 BAA10g26800 A10 21105137 C T missense_variant MODERATE c.692C>T|p.Ala231Val S33
141762 BAA10g26800 A10 21105242 C T missense_variant MODERATE c.797C>T|p.Ala266Val S87
141763 BAA10g26810 A10 21107693 C T missense_variant MODERATE c.148G>A|p.Gly50Ser S127
141764 BAA10g26800 A10 21107835 G A downstream_gene_variant MODIFIER c.*1614G>A| S1
S90
141765 BAA10g26810 A10 21108360 C T upstream_gene_variant MODIFIER c.-430G>A| S265
141766 BAA10g26820 A10 21108612 C T missense_variant MODERATE c.2279G>A|p.Arg760Lys S259
141767 BAA10g26820 A10 21108821 G A synonymous_variant LOW c.2070C>T|p.Asn690Asn S138
141768 BAA10g26820 A10 21109102 C T missense_variant MODERATE c.1789G>A|p.Val597Ile S33
141769 BAA10g26820 A10 21109252 C T missense_variant MODERATE c.1639G>A|p.Glu547Lys S265
141770 BAA10g26820 A10 21109262 C T synonymous_variant LOW c.1629G>A|p.Lys543Lys S185
141771 BAA10g26820 A10 21109357 G A missense_variant MODERATE c.1534C>T|p.Leu512Phe S139
141772 BAA10g26820 A10 21109462 C T missense_variant MODERATE c.1429G>A|p.Asp477Asn S167
141773 BAA10g26820 A10 21109985 C T synonymous_variant LOW c.906G>A|p.Glu302Glu S10
141774 BAA10g26820 A10 21110164 G A stop_gained HIGH c.727C>T|p.Gln243* S103
141775 BAA10g26820 A10 21110588 G A synonymous_variant LOW c.303C>T|p.Phe101Phe S208
S219