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
191201 BAA02g26330 A02 14617357 G A missense_variant MODERATE c.73G>A|p.Glu25Lys S89
191202 BAA02g26330 A02 14617807 G A missense_variant MODERATE c.523G>A|p.Gly175Arg S71
191203 BAA02g26330 A02 14618059 C T stop_gained HIGH c.775C>T|p.Gln259* S63
191204 BAA02g26330 A02 14618263 G A missense_variant MODERATE c.979G>A|p.Glu327Lys S260
191205 BAA02g26330 A02 14618454 C T intron_variant MODIFIER c.1144+26C>T| S9
191206 BAA02g26330 A02 14618652 C T intron_variant MODIFIER c.1144+224C>T| S250
191207 BAA02g26330 A02 14619230 C T missense_variant MODERATE c.1244C>T|p.Ala415Val S33
191208 BAA02g26330 A02 14619340 G A missense_variant MODERATE c.1354G>A|p.Asp452Asn S23
191209 BAA02g26330 A02 14620141 G A intron_variant MODIFIER c.1977+14G>A| S279
191210 BAA02g26330 A02 14620428 G A intron_variant MODIFIER c.2035+78G>A| S100
S251
191211 BAA02g26330 A02 14620482 C A intron_variant MODIFIER c.2036-81C>A| S172
S217
191212 BAA02g26330 A02 14622432 G A splice_region_variant&intron_variant LOW c.3291+6G>A| S150
191213 BAA02g26330 A02 14622462 G A intron_variant MODIFIER c.3291+36G>A| S228
191214 BAA02g26330 A02 14623360 G A missense_variant MODERATE c.3887G>A|p.Ser1296Asn S191
191215 BAA02g26330 A02 14624732 G A downstream_gene_variant MODIFIER c.*1045G>A| S61
191216 BAA02g26330 A02 14624738 G A downstream_gene_variant MODIFIER c.*1051G>A| S223
191217 BAA02g26330 A02 14625911 G A downstream_gene_variant MODIFIER c.*2224G>A| S132
S137
S215
S89
191218 BAA02g26330 A02 14626312 G A downstream_gene_variant MODIFIER c.*2625G>A| S146
191219 BAA02g26330 A02 14626335 C T downstream_gene_variant MODIFIER c.*2648C>T| S296
191220 BAA02g26330 A02 14626804 G A downstream_gene_variant MODIFIER c.*3117G>A| S269
191221 BAA02g26330 A02 14627486 C T downstream_gene_variant MODIFIER c.*3799C>T| S177
191222 BAA02g26330 A02 14627536 C T downstream_gene_variant MODIFIER c.*3849C>T| S33
191223 BAA02g26330 A02 14627858 C T downstream_gene_variant MODIFIER c.*4171C>T| S274
191224 BAA02g26330 A02 14628329 G A downstream_gene_variant MODIFIER c.*4642G>A| S229
191225 BAA02g26330 A02 14628347 C T downstream_gene_variant MODIFIER c.*4660C>T| S207