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
156351 BAA02g04350 A02 1899286 G A upstream_gene_variant MODIFIER c.-2703C>T| S266
156352 BAA02g04350 A02 1900287 G A upstream_gene_variant MODIFIER c.-3704C>T| S166
156353 BAA02g04350 A02 1900862 C T upstream_gene_variant MODIFIER c.-4279G>A| S212
156354 BAA02g04380 A02 1901941 C T upstream_gene_variant MODIFIER c.-1583C>T| S263
156355 BAA02g04380 A02 1902023 G A upstream_gene_variant MODIFIER c.-1501G>A| S53
156356 BAA02g04380 A02 1902413 G A upstream_gene_variant MODIFIER c.-1111G>A| S264
156357 BAA02g04390 A02 1903952 G A upstream_gene_variant MODIFIER c.-4020G>A| S89
156358 BAA02g04390 A02 1904421 C T upstream_gene_variant MODIFIER c.-3551C>T| S171
156359 BAA02g04380 A02 1904438 G A missense_variant MODERATE c.344G>A|p.Arg115Lys S279
156360 BAA02g04390 A02 1904625 C T upstream_gene_variant MODIFIER c.-3347C>T| S159
156361 BAA02g04380 A02 1905049 G A synonymous_variant LOW c.771G>A|p.Glu257Glu S4
156362 BAA02g04380 A02 1905403 G A splice_region_variant&synonymous_variant LOW c.915G>A|p.Gln305Gln S12
156363 BAA02g04390 A02 1907467 C T upstream_gene_variant MODIFIER c.-505C>T| S77
S82
156364 BAA02g04380 A02 1908185 G A downstream_gene_variant MODIFIER c.*1090G>A| S68
156365 BAA02g04380 A02 1908209 C T downstream_gene_variant MODIFIER c.*1114C>T| S100
156366 BAA02g04390 A02 1909112 C T synonymous_variant LOW c.423C>T|p.Leu141Leu S288
156367 BAA02g04390 A02 1909411 C T synonymous_variant LOW c.639C>T|p.Arg213Arg S174
S39
156368 BAA02g04390 A02 1909455 G A missense_variant MODERATE c.683G>A|p.Ser228Asn S64
156369 BAA02g04380 A02 1910010 C T downstream_gene_variant MODIFIER c.*2915C>T| S221
156370 BAA02g04390 A02 1910282 C T missense_variant MODERATE c.1151C>T|p.Pro384Leu S150
156371 BAA02g04390 A02 1910303 G A missense_variant MODERATE c.1172G>A|p.Ser391Asn S155
S211
156372 BAA02g04400 A02 1911851 C T synonymous_variant LOW c.1350G>A|p.Arg450Arg S234
156373 BAA02g04400 A02 1912367 C T synonymous_variant LOW c.834G>A|p.Lys278Lys S80
156374 BAA02g04400 A02 1912482 C T missense_variant MODERATE c.719G>A|p.Gly240Glu S116
156375 BAA02g04400 A02 1912549 C T missense_variant MODERATE c.652G>A|p.Glu218Lys S6