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
166851 BAA02g12820 A02 5746251 C T missense_variant MODERATE c.1427C>T|p.Ser476Leu S270
166852 BAA02g12820 A02 5746432 G A missense_variant&splice_region_variant MODERATE c.1513G>A|p.Glu505Lys S298
166853 BAA02g12810 A02 5747081 C T downstream_gene_variant MODIFIER c.*4200C>T| S230
166854 BAA02g12830 A02 5747214 C T synonymous_variant LOW c.2097G>A|p.Thr699Thr S212
166855 BAA02g12830 A02 5747545 G A missense_variant MODERATE c.1766C>T|p.Ser589Phe S187
166856 BAA02g12830 A02 5748291 C T missense_variant MODERATE c.1186G>A|p.Glu396Lys S75
166857 BAA02g12830 A02 5749000 C T missense_variant MODERATE c.647G>A|p.Arg216Lys S263
166858 BAA02g12830 A02 5749168 C T missense_variant MODERATE c.560G>A|p.Arg187Lys S242
166859 BAA02g12830 A02 5749523 G A missense_variant MODERATE c.205C>T|p.Leu69Phe S60
166860 BAA02g12830 A02 5749676 G A synonymous_variant LOW c.52C>T|p.Leu18Leu S164
166861 BAA02g12830 A02 5750529 C T upstream_gene_variant MODIFIER c.-715G>A| S13
166862 BAA02g12830 A02 5750611 C T upstream_gene_variant MODIFIER c.-797G>A| S266
166863 BAA02g12840 A02 5751111 G A missense_variant MODERATE c.1033C>T|p.Pro345Ser S282
166864 BAA02g12830 A02 5751689 C T upstream_gene_variant MODIFIER c.-1875G>A| S32
166865 BAA02g12840 A02 5752272 G A missense_variant MODERATE c.125C>T|p.Ser42Phe S303
166866 BAA02g12840 A02 5752467 G A synonymous_variant LOW c.21C>T|p.Thr7Thr S286
166867 BAA02g12830 A02 5752488 C T upstream_gene_variant MODIFIER c.-2674G>A| S306
S308
166868 BAA02g12830 A02 5753230 C T upstream_gene_variant MODIFIER c.-3416G>A| S266
166869 BAA02g12830 A02 5753391 C T upstream_gene_variant MODIFIER c.-3577G>A| S78
S83
166870 BAA02g12830 A02 5753661 C T upstream_gene_variant MODIFIER c.-3847G>A| S158
166871 BAA02g12830 A02 5753915 C T upstream_gene_variant MODIFIER c.-4101G>A| S172
S217
166872 BAA02g12850 A02 5753994 C T synonymous_variant LOW c.36C>T|p.Asn12Asn S46
166873 BAA02g12850 A02 5754077 C T splice_region_variant&intron_variant LOW c.111+8C>T| S116
166874 BAA02g12840 A02 5755200 C T upstream_gene_variant MODIFIER c.-2713G>A| S212
166875 BAA02g12860 A02 5756219 G A synonymous_variant LOW c.46C>T|p.Leu16Leu S303