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
76851 BAA01g40620 A01 26892666 G A upstream_gene_variant MODIFIER c.-4772G>A| S135
76852 BAA01g40600 A01 26892980 G A missense_variant MODERATE c.2014C>T|p.Pro672Ser S67
76853 BAA01g40600 A01 26893219 C T missense_variant MODERATE c.1775G>A|p.Arg592Lys S206
S26
76854 BAA01g40600 A01 26896405 C T upstream_gene_variant MODIFIER c.-1412G>A| S59
76855 BAA01g40600 A01 26896710 A T upstream_gene_variant MODIFIER c.-1717T>A| S14
76856 BAA01g40600 A01 26896849 C T upstream_gene_variant MODIFIER c.-1856G>A| S68
76857 BAA01g40600 A01 26897245 C T upstream_gene_variant MODIFIER c.-2252G>A| S133
76858 BAA01g40600 A01 26897413 C T upstream_gene_variant MODIFIER c.-2420G>A| S242
76859 BAA01g40600 A01 26897923 G A upstream_gene_variant MODIFIER c.-2930C>T| S77
76860 BAA01g40630 A01 26900764 G A missense_variant MODERATE c.316G>A|p.Glu106Lys S175
76861 BAA01g40610 A01 26900800 C T upstream_gene_variant MODIFIER c.-4572G>A| S23
76862 BAA01g40610 A01 26900878 G A upstream_gene_variant MODIFIER c.-4650C>T| S37
76863 BAA01g40640 A01 26901452 G A upstream_gene_variant MODIFIER c.-1351G>A| S106
76864 BAA01g40640 A01 26902627 G A upstream_gene_variant MODIFIER c.-176G>A| S208
S219
76865 BAA01g40640 A01 26902635 G A upstream_gene_variant MODIFIER c.-168G>A| S149
76866 BAA01g40640 A01 26902639 C T upstream_gene_variant MODIFIER c.-164C>T| S92
76867 BAA01g40640 A01 26903368 G A synonymous_variant LOW c.291G>A|p.Lys97Lys S173
76868 BAA01g40640 A01 26903428 C T synonymous_variant LOW c.351C>T|p.Cys117Cys S59
76869 BAA01g40620 A01 26903782 G A downstream_gene_variant MODIFIER c.*4073G>A| S262
76870 BAA01g40620 A01 26904577 C T downstream_gene_variant MODIFIER c.*4868C>T| S246
76871 BAA01g40650 A01 26906500 C T downstream_gene_variant MODIFIER c.*2528G>A| S64
76872 BAA01g40650 A01 26907209 A T downstream_gene_variant MODIFIER c.*1819T>A| S213
76873 BAA01g40640 A01 26907530 C T synonymous_variant LOW c.816C>T|p.Phe272Phe S132
S137
S215
76874 BAA01g40640 A01 26907681 G A missense_variant MODERATE c.967G>A|p.Glu323Lys S238
76875 BAA01g40640 A01 26907693 G A missense_variant MODERATE c.979G>A|p.Glu327Lys S217
S248