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
158201 BAA02g05860 A02 2497863 G A splice_region_variant&intron_variant LOW c.568-5C>T| S210
158202 BAA02g05860 A02 2498486 G A synonymous_variant LOW c.199C>T|p.Leu67Leu S166
158203 BAA02g05860 A02 2498571 C T synonymous_variant LOW c.114G>A|p.Glu38Glu S212
158204 BAA02g05860 A02 2498694 C T missense_variant MODERATE c.89G>A|p.Arg30Lys S260
158205 BAA02g05860 A02 2499245 C T upstream_gene_variant MODIFIER c.-463G>A| S13
158206 BAA02g05860 A02 2499271 G A upstream_gene_variant MODIFIER c.-489C>T| S113
158207 BAA02g05860 A02 2499311 G A upstream_gene_variant MODIFIER c.-529C>T| S210
158208 BAA02g05860 A02 2499523 C T upstream_gene_variant MODIFIER c.-741G>A| S97
158209 BAA02g05860 A02 2499617 G A upstream_gene_variant MODIFIER c.-835C>T| S281
158210 BAA02g05860 A02 2499864 C T upstream_gene_variant MODIFIER c.-1082G>A| S295
158211 BAA02g05860 A02 2499924 G A upstream_gene_variant MODIFIER c.-1142C>T| S237
158212 BAA02g05870 A02 2501192 C T missense_variant MODERATE c.101C>T|p.Ser34Leu S80
158213 BAA02g05860 A02 2501257 C T upstream_gene_variant MODIFIER c.-2475G>A| S275
158214 BAA02g05860 A02 2502324 G A upstream_gene_variant MODIFIER c.-3542C>T| S187
158215 BAA02g05870 A02 2502478 G A missense_variant MODERATE c.604G>A|p.Glu202Lys S305
158216 BAA02g05860 A02 2503093 G A upstream_gene_variant MODIFIER c.-4311C>T| S23
158217 BAA02g05860 A02 2503571 A T upstream_gene_variant MODIFIER c.-4789T>A| S64
158218 BAA02g05860 A02 2503620 C T upstream_gene_variant MODIFIER c.-4838G>A| S182
158219 BAA02g05860 A02 2503685 G A upstream_gene_variant MODIFIER c.-4903C>T| S237
158220 BAA02g05870 A02 2504149 G A downstream_gene_variant MODIFIER c.*1609G>A| S45
158221 BAA02g05880 A02 2506487 C T upstream_gene_variant MODIFIER c.-1301G>A| S200
158222 BAA02g05880 A02 2508021 C T upstream_gene_variant MODIFIER c.-2835G>A| S276
158223 BAA02g05900 A02 2508101 C T stop_gained HIGH c.813G>A|p.Trp271* S25
158224 BAA02g05900 A02 2508626 C T missense_variant MODERATE c.524G>A|p.Gly175Glu S181
158225 BAA02g05900 A02 2508686 C T missense_variant MODERATE c.464G>A|p.Arg155His S121