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
153251 BAA02g01760 A02 779042 C T upstream_gene_variant MODIFIER c.-1713G>A| S61
153252 BAA02g01770 A02 779962 C T synonymous_variant LOW c.2649G>A|p.Arg883Arg S183
S198
153253 BAA02g01770 A02 780163 C T synonymous_variant LOW c.2448G>A|p.Glu816Glu S83
S88
153254 BAA02g01760 A02 780766 C T upstream_gene_variant MODIFIER c.-3437G>A| S116
153255 BAA02g01760 A02 781759 G A upstream_gene_variant MODIFIER c.-4430C>T| S226
153256 BAA02g01780 A02 782779 T C downstream_gene_variant MODIFIER c.*3898A>G| S197
153257 BAA02g01780 A02 782921 C T downstream_gene_variant MODIFIER c.*3756G>A| S240
153258 BAA02g01770 A02 783037 G A missense_variant MODERATE c.1910C>T|p.Ser637Phe S286
153259 BAA02g01770 A02 783408 G A synonymous_variant LOW c.1539C>T|p.His513His S68
153260 BAA02g01790 A02 784928 C T upstream_gene_variant MODIFIER c.-4352C>T| S182
153261 BAA02g01790 A02 785056 C T upstream_gene_variant MODIFIER c.-4224C>T| S298
153262 BAA02g01770 A02 785526 C T synonymous_variant LOW c.1053G>A|p.Glu351Glu S61
153263 BAA02g01770 A02 785920 C T missense_variant MODERATE c.659G>A|p.Arg220Lys S207
153264 BAA02g01770 A02 786225 C T synonymous_variant LOW c.354G>A|p.Leu118Leu S262
153265 BAA02g01770 A02 786560 C T missense_variant MODERATE c.19G>A|p.Asp7Asn S262
153266 BAA02g01780 A02 787744 G A synonymous_variant LOW c.762C>T|p.Leu254Leu S202
153267 BAA02g01780 A02 787797 G A stop_gained HIGH c.709C>T|p.Arg237* S204
153268 BAA02g01770 A02 788574 G A upstream_gene_variant MODIFIER c.-1996C>T| S273
153269 BAA02g01790 A02 789299 C T missense_variant MODERATE c.20C>T|p.Ala7Val S255
153270 BAA02g01770 A02 789449 C T upstream_gene_variant MODIFIER c.-2871G>A| S272
153271 BAA02g01790 A02 789785 C T synonymous_variant LOW c.306C>T|p.Ile102Ile S37
153272 BAA02g01800 A02 791157 C T stop_gained&splice_region_variant HIGH c.510G>A|p.Trp170* S251
153273 BAA02g01800 A02 791967 C T missense_variant MODERATE c.181G>A|p.Gly61Arg S18
153274 BAA02g01800 A02 796398 G A upstream_gene_variant MODIFIER c.-4176C>T| S293
153275 BAA02g01800 A02 796865 G A upstream_gene_variant MODIFIER c.-4643C>T| S188