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
152051 BAA02g00640 A02 342856 G A downstream_gene_variant MODIFIER c.*2429G>A| S25
152052 BAA02g00660 A02 343104 C T missense_variant MODERATE c.1075G>A|p.Val359Ile S186
152053 BAA02g00660 A02 343755 C T stop_gained HIGH c.504G>A|p.Trp168* S131
152054 BAA02g00660 A02 343979 G A missense_variant MODERATE c.367C>T|p.His123Tyr S202
152055 BAA02g00660 A02 344892 G A missense_variant MODERATE c.41C>T|p.Thr14Ile S293
152056 BAA02g00660 A02 345316 G A upstream_gene_variant MODIFIER c.-384C>T| S289
S290
152057 BAA02g00660 A02 345891 G A upstream_gene_variant MODIFIER c.-959C>T| S105
S106
152058 BAA02g00670 A02 347445 C T missense_variant MODERATE c.716G>A|p.Gly239Asp S157
152059 BAA02g00660 A02 348175 C T upstream_gene_variant MODIFIER c.-3243G>A| S167
152060 BAA02g00670 A02 348271 G A synonymous_variant LOW c.183C>T|p.Thr61Thr S286
152061 BAA02g00670 A02 348392 C T missense_variant MODERATE c.62G>A|p.Gly21Glu S1
S90
152062 BAA02g00660 A02 348496 G A upstream_gene_variant MODIFIER c.-3564C>T| S96
152063 BAA02g00660 A02 349861 G A upstream_gene_variant MODIFIER c.-4929C>T| S161
152064 BAA02g00660 A02 349925 C T upstream_gene_variant MODIFIER c.-4993G>A| S150
152065 BAA02g00680 A02 351649 C T missense_variant MODERATE c.1046C>T|p.Ser349Phe S142
152066 BAA02g00680 A02 351744 G A missense_variant MODERATE c.1141G>A|p.Val381Ile S163
152067 BAA02g00670 A02 352336 G A upstream_gene_variant MODIFIER c.-3883C>T| S242
152068 BAA02g00680 A02 352618 C T missense_variant MODERATE c.1709C>T|p.Ser570Phe S257
152069 BAA02g00690 A02 353654 C T downstream_gene_variant MODIFIER c.*4128G>A| S104
152070 BAA02g00680 A02 353977 C T synonymous_variant LOW c.2724C>T|p.Thr908Thr S186
152071 BAA02g00680 A02 354178 C T synonymous_variant LOW c.2925C>T|p.Leu975Leu S234
152072 BAA02g00680 A02 354378 G A missense_variant MODERATE c.3125G>A|p.Cys1042Tyr S9
152073 BAA02g00680 A02 355213 G A synonymous_variant LOW c.3876G>A|p.Thr1292Thr S209
152074 BAA02g00680 A02 356122 G A synonymous_variant LOW c.4335G>A|p.Val1445Val S126
152075 BAA02g00680 A02 357480 G A downstream_gene_variant MODIFIER c.*1132G>A| S45