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
162051 BAA02g09000 A02 3990649 G A downstream_gene_variant MODIFIER c.*2366G>A| S41
162052 BAA02g09020 A02 3991025 G A missense_variant MODERATE c.314C>T|p.Pro105Leu S282
162053 BAA02g09020 A02 3991343 C T splice_region_variant&synonymous_variant LOW c.204G>A|p.Lys68Lys S128
162054 BAA02g09020 A02 3992053 C T upstream_gene_variant MODIFIER c.-202G>A| S216
162055 BAA02g09020 A02 3992723 G A upstream_gene_variant MODIFIER c.-872C>T| S184
162056 BAA02g09020 A02 3992757 G A upstream_gene_variant MODIFIER c.-906C>T| S11
162057 BAA02g09020 A02 3992864 G T upstream_gene_variant MODIFIER c.-1013C>A| S170
S228
S263
S275
S41
162058 BAA02g09030 A02 3993150 C T synonymous_variant LOW c.1116G>A|p.Gln372Gln S75
S81
162059 BAA02g09030 A02 3993474 G A missense_variant MODERATE c.881C>T|p.Ala294Val S291
162060 BAA02g09030 A02 3993493 T A missense_variant MODERATE c.862A>T|p.Ile288Phe S255
162061 BAA02g09030 A02 3993650 G A synonymous_variant LOW c.705C>T|p.Ile235Ile S61
162062 BAA02g09020 A02 3995716 G A upstream_gene_variant MODIFIER c.-3865C>T| S125
162063 BAA02g09020 A02 3996711 C T upstream_gene_variant MODIFIER c.-4860G>A| S257
162064 BAA02g09020 A02 3996718 C T upstream_gene_variant MODIFIER c.-4867G>A| S1
162065 BAA02g09020 A02 3996849 C T upstream_gene_variant MODIFIER c.-4998G>A| S28
162066 BAA02g09030 A02 3996969 G A upstream_gene_variant MODIFIER c.-2385C>T| S229
162067 BAA02g09030 A02 3997245 C T upstream_gene_variant MODIFIER c.-2661G>A| S195
162068 BAA02g09030 A02 3997969 C T upstream_gene_variant MODIFIER c.-3385G>A| S56
162069 BAA02g09030 A02 3998059 C T upstream_gene_variant MODIFIER c.-3475G>A| S255
162070 BAA02g09030 A02 3998761 C T upstream_gene_variant MODIFIER c.-4177G>A| S277
162071 BAA02g09040 A02 3999297 C T missense_variant MODERATE c.517C>T|p.Pro173Ser S18
162072 BAA02g09040 A02 3999546 C T stop_gained HIGH c.697C>T|p.Gln233* S263
162073 BAA02g09040 A02 3999691 C T missense_variant MODERATE c.842C>T|p.Ala281Val S293
162074 BAA02g09040 A02 3999738 G A missense_variant MODERATE c.889G>A|p.Glu297Lys S202
162075 BAA02g09040 A02 4000050 C T synonymous_variant LOW c.1113C>T|p.Val371Val S120