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
162701 BAA02g09590 A02 4221587 G A missense_variant MODERATE c.215G>A|p.Arg72Lys S51
162702 BAA02g09590 A02 4222043 G A missense_variant MODERATE c.671G>A|p.Gly224Glu S17
162703 BAA02g09590 A02 4223050 G A missense_variant MODERATE c.1678G>A|p.Glu560Lys S37
162704 BAA02g09590 A02 4223370 G A synonymous_variant LOW c.1998G>A|p.Glu666Glu S150
162705 BAA02g09590 A02 4224006 G A missense_variant MODERATE c.2545G>A|p.Asp849Asn S153
S213
162706 BAA02g09620 A02 4224994 C T upstream_gene_variant MODIFIER c.-4364C>T| S301
S304
162707 BAA02g09600 A02 4225984 G A upstream_gene_variant MODIFIER c.-275C>T| S132
S137
S215
S89
162708 BAA02g09600 A02 4226263 C T upstream_gene_variant MODIFIER c.-554G>A| S38
162709 BAA02g09600 A02 4226992 G A upstream_gene_variant MODIFIER c.-1283C>T| S109
162710 BAA02g09610 A02 4228057 C T missense_variant MODERATE c.280G>A|p.Asp94Asn S28
162711 BAA02g09610 A02 4231095 G A upstream_gene_variant MODIFIER c.-2759C>T| S37
162712 BAA02g09610 A02 4231097 G A upstream_gene_variant MODIFIER c.-2761C>T| S236
162713 BAA02g09630 A02 4231790 G A missense_variant MODERATE c.530C>T|p.Pro177Leu S143
162714 BAA02g09630 A02 4232049 C T missense_variant MODERATE c.271G>A|p.Val91Ile S233
162715 BAA02g09630 A02 4232084 G A missense_variant MODERATE c.236C>T|p.Ala79Val S7
162716 BAA02g09630 A02 4233955 C T upstream_gene_variant MODIFIER c.-1636G>A| S230
162717 BAA02g09630 A02 4234023 C T upstream_gene_variant MODIFIER c.-1704G>A| S157
162718 BAA02g09630 A02 4234970 G A upstream_gene_variant MODIFIER c.-2651C>T| S207
162719 BAA02g09630 A02 4235942 G A upstream_gene_variant MODIFIER c.-3623C>T| S282
162720 BAA02g09640 A02 4236760 G A synonymous_variant LOW c.687C>T|p.Cys229Cys S136
162721 BAA02g09640 A02 4237444 G A splice_region_variant&intron_variant LOW c.273-8C>T| S200
S261
S303
162722 BAA02g09640 A02 4237533 G A missense_variant&splice_region_variant MODERATE c.272C>T|p.Ala91Val S171
162723 BAA02g09650 A02 4238353 G A upstream_gene_variant MODIFIER c.-2561G>A| S168
S219
S279
162724 BAA02g09650 A02 4238983 G A upstream_gene_variant MODIFIER c.-1931G>A| S165
162725 BAA02g09650 A02 4239011 C T upstream_gene_variant MODIFIER c.-1903C>T| S278