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
168201 BAA02g13570 A02 6291889 G A downstream_gene_variant MODIFIER c.*814G>A| S282
168202 BAA02g13590 A02 6293669 C T upstream_gene_variant MODIFIER c.-3982C>T| S165
168203 BAA02g13590 A02 6293776 G A upstream_gene_variant MODIFIER c.-3875G>A| S288
168204 BAA02g13590 A02 6294616 C T upstream_gene_variant MODIFIER c.-3035C>T| S280
168205 BAA02g13590 A02 6295213 G A upstream_gene_variant MODIFIER c.-2438G>A| S174
168206 BAA02g13580 A02 6296544 C T missense_variant MODERATE c.236G>A|p.Arg79Lys S283
168207 BAA02g13580 A02 6297115 G A missense_variant MODERATE c.160C>T|p.Leu54Phe S113
168208 BAA02g13590 A02 6297690 C T missense_variant MODERATE c.40C>T|p.His14Tyr S208
S219
168209 BAA02g13580 A02 6297846 C T upstream_gene_variant MODIFIER c.-487G>A| S127
168210 BAA02g13590 A02 6299009 C T missense_variant MODERATE c.1087C>T|p.Leu363Phe S178
168211 BAA02g13590 A02 6299133 C T synonymous_variant LOW c.1119C>T|p.Cys373Cys S301
S304
168212 BAA02g13580 A02 6300414 C T upstream_gene_variant MODIFIER c.-3055G>A| S58
168213 BAA02g13580 A02 6300949 G A upstream_gene_variant MODIFIER c.-3590C>T| S187
168214 BAA02g13600 A02 6302702 G A upstream_gene_variant MODIFIER c.-2203G>A| S168
168215 BAA02g13590 A02 6305048 G A downstream_gene_variant MODIFIER c.*4797G>A| S198
168216 BAA02g13600 A02 6305814 C T missense_variant MODERATE c.472C>T|p.Pro158Ser S94
168217 BAA02g13600 A02 6306012 C T missense_variant MODERATE c.575C>T|p.Pro192Leu S283
168218 BAA02g13600 A02 6306293 C T missense_variant MODERATE c.769C>T|p.Pro257Ser S81
168219 BAA02g13600 A02 6306543 C T missense_variant MODERATE c.935C>T|p.Pro312Leu S255
168220 BAA02g13600 A02 6306843 C T stop_gained HIGH c.1156C>T|p.Gln386* S200
168221 BAA02g13600 A02 6306882 C T missense_variant MODERATE c.1195C>T|p.Leu399Phe S1
S90
168222 BAA02g13600 A02 6306890 C T synonymous_variant LOW c.1203C>T|p.Asp401Asp S221
168223 BAA02g13600 A02 6307232 G A synonymous_variant LOW c.1545G>A|p.Gly515Gly S237
168224 BAA02g13600 A02 6307298 G A synonymous_variant LOW c.1611G>A|p.Lys537Lys S25
168225 BAA02g13600 A02 6308041 G A intron_variant MODIFIER c.2008+209G>A| S218
S267
S268
S269