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
172051 BAA02g15970 A02 7772454 G A upstream_gene_variant MODIFIER c.-1673G>A| S264
172052 BAA02g15960 A02 7773536 G A upstream_gene_variant MODIFIER c.-460C>T| S264
172053 BAA02g15960 A02 7774255 A G upstream_gene_variant MODIFIER c.-1179T>C| S162
172054 BAA02g15960 A02 7774460 C T upstream_gene_variant MODIFIER c.-1384G>A| S15
S2
S3
S34
S4
S6
172055 BAA02g15970 A02 7774493 C T missense_variant MODERATE c.245C>T|p.Ala82Val S100
172056 BAA02g15970 A02 7774582 G A missense_variant MODERATE c.334G>A|p.Glu112Lys S52
172057 BAA02g15960 A02 7775865 C T upstream_gene_variant MODIFIER c.-2789G>A| S18
172058 BAA02g15960 A02 7776232 G A upstream_gene_variant MODIFIER c.-3156C>T| S125
172059 BAA02g15960 A02 7777510 G A upstream_gene_variant MODIFIER c.-4434C>T| S33
172060 BAA02g15960 A02 7777708 G A upstream_gene_variant MODIFIER c.-4632C>T| S224
172061 BAA02g15960 A02 7777783 G A upstream_gene_variant MODIFIER c.-4707C>T| S187
172062 BAA02g15970 A02 7778400 G A missense_variant MODERATE c.1225G>A|p.Ala409Thr S140
S219
S278
S64
172063 BAA02g15970 A02 7779062 G A missense_variant MODERATE c.1684G>A|p.Asp562Asn S256
172064 BAA02g15970 A02 7779352 G A synonymous_variant LOW c.1974G>A|p.Arg658Arg S245
172065 BAA02g15970 A02 7779510 C T missense_variant MODERATE c.2132C>T|p.Pro711Leu S183
S198
172066 BAA02g15970 A02 7779590 C G missense_variant MODERATE c.2212C>G|p.Pro738Ala S250
S296
172067 BAA02g15970 A02 7780836 G A missense_variant MODERATE c.3430G>A|p.Glu1144Lys S57
172068 BAA02g15970 A02 7781740 T C synonymous_variant LOW c.4302T>C|p.Asp1434Asp S278
172069 BAA02g15970 A02 7782536 G A synonymous_variant LOW c.4350G>A|p.Glu1450Glu S48
172070 BAA02g15970 A02 7782600 C T missense_variant MODERATE c.4414C>T|p.Pro1472Ser S105
S106
172071 BAA02g15970 A02 7782726 G A missense_variant MODERATE c.4540G>A|p.Ala1514Thr S190
172072 BAA02g15970 A02 7782922 C T missense_variant MODERATE c.4736C>T|p.Thr1579Ile S130
172073 BAA02g15970 A02 7783323 G A missense_variant MODERATE c.5137G>A|p.Glu1713Lys S10
S190
172074 BAA02g15970 A02 7783404 G A missense_variant MODERATE c.5218G>A|p.Asp1740Asn S33
172075 BAA02g15970 A02 7783506 C T downstream_gene_variant MODIFIER c.*49C>T| S262