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
175401 BAA02g17840 A02 8913397 C T downstream_gene_variant MODIFIER c.*2674G>A| S293
175402 BAA02g17840 A02 8913560 G A downstream_gene_variant MODIFIER c.*2511C>T| S191
175403 BAA02g17840 A02 8913927 C T downstream_gene_variant MODIFIER c.*2144G>A| S270
175404 BAA02g17840 A02 8913972 C A downstream_gene_variant MODIFIER c.*2099G>T| S16
175405 BAA02g17840 A02 8914738 C T downstream_gene_variant MODIFIER c.*1333G>A| S224
175406 BAA02g17840 A02 8917230 C T upstream_gene_variant MODIFIER c.-440G>A| S94
175407 BAA02g17840 A02 8917254 C T upstream_gene_variant MODIFIER c.-464G>A| S171
175408 BAA02g17840 A02 8918521 T A upstream_gene_variant MODIFIER c.-1731A>T| S242
175409 BAA02g17840 A02 8919980 C T upstream_gene_variant MODIFIER c.-3190G>A| S118
175410 BAA02g17840 A02 8920094 C T upstream_gene_variant MODIFIER c.-3304G>A| S241
175411 BAA02g17840 A02 8920890 G A upstream_gene_variant MODIFIER c.-4100C>T| S148
S210
S30
S31
175412 BAA02g17850 A02 8926126 C T upstream_gene_variant MODIFIER c.-609C>T| S177
175413 BAA02g17850 A02 8926642 G A upstream_gene_variant MODIFIER c.-93G>A| S129
175414 BAA02g17850 A02 8926817 C T missense_variant MODERATE c.83C>T|p.Ser28Phe S130
175415 BAA02g17850 A02 8927770 C T downstream_gene_variant MODIFIER c.*394C>T| S124
175416 BAA02g17850 A02 8927775 T G downstream_gene_variant MODIFIER c.*399T>G| S127
S129
S152
S236
S62
175417 BAA02g17850 A02 8928347 G A downstream_gene_variant MODIFIER c.*971G>A| S240
175418 BAA02g17860 A02 8933333 C T downstream_gene_variant MODIFIER c.*1734G>A| S218
175419 BAA02g17860 A02 8933543 C T downstream_gene_variant MODIFIER c.*1524G>A| S277
175420 BAA02g17860 A02 8933688 C T downstream_gene_variant MODIFIER c.*1379G>A| S261
175421 BAA02g17860 A02 8933765 C T downstream_gene_variant MODIFIER c.*1302G>A| S178
175422 BAA02g17860 A02 8934488 C T downstream_gene_variant MODIFIER c.*579G>A| S266
175423 BAA02g17860 A02 8935308 C T missense_variant MODERATE c.815G>A|p.Gly272Glu S25
175424 BAA02g17860 A02 8935410 C T missense_variant MODERATE c.713G>A|p.Gly238Asp S115
175425 BAA02g17870 A02 8936171 G A downstream_gene_variant MODIFIER c.*2149C>T| S53