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
162201 BAA02g09150 A02 4050692 G A upstream_gene_variant MODIFIER c.-3190C>T| S235
162202 BAA02g09150 A02 4050780 G A upstream_gene_variant MODIFIER c.-3278C>T| S17
162203 BAA02g09150 A02 4050800 G A upstream_gene_variant MODIFIER c.-3298C>T| S164
162204 BAA02g09150 A02 4052026 G A upstream_gene_variant MODIFIER c.-4524C>T| S269
162205 BAA02g09160 A02 4052611 C T synonymous_variant LOW c.975G>A|p.Glu325Glu S183
S198
162206 BAA02g09160 A02 4052698 C T synonymous_variant LOW c.888G>A|p.Thr296Thr S273
162207 BAA02g09160 A02 4053355 C T stop_gained HIGH c.231G>A|p.Trp77* S202
162208 BAA02g09160 A02 4053456 G A missense_variant MODERATE c.130C>T|p.Pro44Ser S5
162209 BAA02g09160 A02 4053510 G A stop_gained HIGH c.76C>T|p.Gln26* S168
162210 BAA02g09160 A02 4053538 C T missense_variant MODERATE c.48G>A|p.Met16Ile S277
162211 BAA02g09160 A02 4056436 C T upstream_gene_variant MODIFIER c.-2851G>A| S205
S240
162212 BAA02g09160 A02 4058020 T C upstream_gene_variant MODIFIER c.-4435A>G| S18
162213 BAA02g09160 A02 4058068 G T upstream_gene_variant MODIFIER c.-4483C>A| S40
S49
162214 BAA02g09160 A02 4058107 C T upstream_gene_variant MODIFIER c.-4522G>A| S138
162215 BAA02g09170 A02 4059008 G A upstream_gene_variant MODIFIER c.-1803C>T| S149
162216 BAA02g09180 A02 4060933 C T missense_variant MODERATE c.175G>A|p.Glu59Lys S144
S95
162217 BAA02g09190 A02 4062163 C T synonymous_variant LOW c.1746G>A|p.Gly582Gly S6
162218 BAA02g09190 A02 4063346 C T synonymous_variant LOW c.957G>A|p.Gln319Gln S268
162219 BAA02g09190 A02 4063782 G A missense_variant MODERATE c.802C>T|p.His268Tyr S18
S221
S252
162220 BAA02g09180 A02 4063936 G A upstream_gene_variant MODIFIER c.-2674C>T| S235
162221 BAA02g09190 A02 4064869 C A missense_variant MODERATE c.11G>T|p.Arg4Leu S241
162222 BAA02g09180 A02 4065438 C T upstream_gene_variant MODIFIER c.-4176G>A| S224
162223 BAA02g09200 A02 4066504 C T missense_variant MODERATE c.232C>T|p.Arg78Cys S138
162224 BAA02g09190 A02 4067126 G A upstream_gene_variant MODIFIER c.-2247C>T| S69
162225 BAA02g09190 A02 4068370 C T upstream_gene_variant MODIFIER c.-3491G>A| S286