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
152351 BAA02g00970 A02 455045 G A upstream_gene_variant MODIFIER c.-1629C>T| S289
S290
152352 BAA02g00980 A02 456963 C T splice_region_variant&intron_variant LOW c.807-6G>A| S65
152353 BAA02g00980 A02 457314 G A synonymous_variant LOW c.525C>T|p.Leu175Leu S80
152354 BAA02g00970 A02 457788 G A upstream_gene_variant MODIFIER c.-4372C>T| S295
152355 BAA02g00970 A02 458253 C T upstream_gene_variant MODIFIER c.-4837G>A| S37
152356 BAA02g00980 A02 458692 C T upstream_gene_variant MODIFIER c.-188G>A| S144
152357 BAA02g00980 A02 458777 G A upstream_gene_variant MODIFIER c.-273C>T| S95
152358 BAA02g00980 A02 459010 C T upstream_gene_variant MODIFIER c.-506G>A| S306
S308
152359 BAA02g00980 A02 460743 C T upstream_gene_variant MODIFIER c.-2239G>A| S201
152360 BAA02g00990 A02 460926 C T splice_region_variant&intron_variant LOW c.1067+5G>A| S200
152361 BAA02g00990 A02 461189 G A synonymous_variant LOW c.897C>T|p.Leu299Leu S287
152362 BAA02g00980 A02 461473 G A upstream_gene_variant MODIFIER c.-2969C>T| S238
152363 BAA02g00990 A02 461722 G A splice_region_variant&intron_variant LOW c.681+4C>T| S231
152364 BAA02g00990 A02 462376 C T missense_variant MODERATE c.416G>A|p.Gly139Glu S185
152365 BAA02g00990 A02 462933 C T missense_variant MODERATE c.11G>A|p.Arg4His S305
152366 BAA02g00980 A02 463044 G A upstream_gene_variant MODIFIER c.-4540C>T| S259
152367 BAA02g00990 A02 464296 G A upstream_gene_variant MODIFIER c.-1353C>T| S286
152368 BAA02g01010 A02 465592 C T synonymous_variant LOW c.405C>T|p.Phe135Phe S97
152369 BAA02g01010 A02 465622 G A synonymous_variant LOW c.435G>A|p.Glu145Glu S169
152370 BAA02g01010 A02 466220 C T stop_gained HIGH c.1033C>T|p.Gln345* S130
152371 BAA02g01010 A02 466647 G A synonymous_variant LOW c.1284G>A|p.Glu428Glu S239
152372 BAA02g01010 A02 466669 G A missense_variant MODERATE c.1306G>A|p.Glu436Lys S156
152373 BAA02g01010 A02 466743 G A synonymous_variant LOW c.1380G>A|p.Arg460Arg S28
152374 BAA02g00990 A02 467679 C T upstream_gene_variant MODIFIER c.-4736G>A| S18
152375 BAA02g01020 A02 468372 G A upstream_gene_variant MODIFIER c.-747G>A| S23