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
90901 BAA10g00920 A10 428284 G A missense_variant MODERATE c.230C>T|p.Pro77Leu S230
90902 BAA10g00920 A10 428453 C T missense_variant MODERATE c.61G>A|p.Asp21Asn S182
90903 BAA10g00920 A10 429267 C T upstream_gene_variant MODIFIER c.-754G>A| S10
S56
90904 BAA10g00920 A10 430809 C T upstream_gene_variant MODIFIER c.-2296G>A| S180
90905 BAA10g00920 A10 433246 C T upstream_gene_variant MODIFIER c.-4733G>A| S135
90906 BAA10g00920-BAA10g00930 A10 435163 C T intergenic_region MODIFIER n.435163C>T| S139
90907 BAA10g00920-BAA10g00930 A10 435543 G A intergenic_region MODIFIER n.435543G>A| S17
90908 BAA10g00920-BAA10g00930 A10 435657 C T intergenic_region MODIFIER n.435657C>T| S31
90909 BAA10g00920-BAA10g00930 A10 436160 G A intergenic_region MODIFIER n.436160G>A| S159
S243
90910 BAA10g00920-BAA10g00930 A10 436399 C T intergenic_region MODIFIER n.436399C>T| S35
90911 BAA10g00930 A10 438223 G A upstream_gene_variant MODIFIER c.-4926G>A| S164
90912 BAA10g00930 A10 438455 C T upstream_gene_variant MODIFIER c.-4694C>T| S152
90913 BAA10g00930 A10 439768 G A upstream_gene_variant MODIFIER c.-3381G>A| S134
90914 BAA10g00930 A10 439821 G A upstream_gene_variant MODIFIER c.-3328G>A| S128
90915 BAA10g00930 A10 439927 C T upstream_gene_variant MODIFIER c.-3222C>T| S119
90916 BAA10g00930 A10 439940 G A upstream_gene_variant MODIFIER c.-3209G>A| S184
90917 BAA10g00930 A10 440109 G A upstream_gene_variant MODIFIER c.-3040G>A| S18
90918 BAA10g00930 A10 441404 C T upstream_gene_variant MODIFIER c.-1745C>T| S6
90919 BAA10g00930 A10 443881 C T missense_variant MODERATE c.733C>T|p.Pro245Ser S139
90920 BAA10g00930 A10 444105 G A synonymous_variant LOW c.957G>A|p.Ser319Ser S130
90921 BAA10g00940 A10 448580 C T missense_variant MODERATE c.695C>T|p.Ser232Phe S52
90922 BAA10g00930 A10 449038 C T downstream_gene_variant MODIFIER c.*4855C>T| S149
90923 BAA10g00950 A10 449240 G A synonymous_variant LOW c.1398C>T|p.Phe466Phe S127
90924 BAA10g00950 A10 449640 A C missense_variant MODERATE c.1123T>G|p.Tyr375Asp S305
90925 BAA10g00940 A10 450443 G A downstream_gene_variant MODIFIER c.*1826G>A| S19