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
116451 BAA10g10260 A10 12028202 C T upstream_gene_variant MODIFIER c.-2660G>A| S195
116452 BAA10g10260 A10 12028218 C T upstream_gene_variant MODIFIER c.-2676G>A| S168
S70
116453 BAA10g10260 A10 12028233 G A upstream_gene_variant MODIFIER c.-2691C>T| S53
116454 BAA10g10260 A10 12029311 C T upstream_gene_variant MODIFIER c.-3769G>A| S79
S91
116455 BAA10g10270 A10 12030678 G A downstream_gene_variant MODIFIER c.*218G>A| S68
116456 BAA10g10280 A10 12031015 G A stop_gained HIGH c.670C>T|p.Gln224* S95
116457 BAA10g10280 A10 12031136 G A synonymous_variant LOW c.549C>T|p.Asp183Asp S1
116458 BAA10g10270 A10 12031347 G A downstream_gene_variant MODIFIER c.*887G>A| S216
116459 BAA10g10280 A10 12035648 C T upstream_gene_variant MODIFIER c.-3761G>A| S208
S93
116460 BAA10g10280 A10 12036118 C T upstream_gene_variant MODIFIER c.-4231G>A| S176
116461 BAA10g10280 A10 12036831 G A upstream_gene_variant MODIFIER c.-4944C>T| S50
116462 BAA10g10280-BAA10g10290 A10 12038685 G A intergenic_region MODIFIER n.12038685G>A| S59
116463 BAA10g10290 A10 12045035 G A synonymous_variant LOW c.969C>T|p.Ala323Ala S293
116464 BAA10g10290 A10 12045295 G A intron_variant MODIFIER c.725-16C>T| S288
116465 BAA10g10290 A10 12046945 G A missense_variant MODERATE c.719C>T|p.Thr240Ile S202
116466 BAA10g10290 A10 12047416 G A missense_variant MODERATE c.248C>T|p.Pro83Leu S126
S61
116467 BAA10g10290 A10 12047443 T A missense_variant MODERATE c.221A>T|p.Glu74Val S299
116468 BAA10g10290 A10 12048757 C T upstream_gene_variant MODIFIER c.-988G>A| S203
116469 BAA10g10290 A10 12049943 G A upstream_gene_variant MODIFIER c.-2174C>T| S62
116470 BAA10g10290 A10 12050339 C T upstream_gene_variant MODIFIER c.-2570G>A| S199
116471 BAA10g10290 A10 12051466 C T upstream_gene_variant MODIFIER c.-3697G>A| S259
116472 BAA10g10290 A10 12051598 G A upstream_gene_variant MODIFIER c.-3829C>T| S157
S163
116473 BAA10g10290 A10 12052144 C T upstream_gene_variant MODIFIER c.-4375G>A| S169
116474 BAA10g10300 A10 12052998 G A upstream_gene_variant MODIFIER c.-2359G>A| S262
116475 BAA10g10300 A10 12053381 C T upstream_gene_variant MODIFIER c.-1976C>T| S199