Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 13 of 13 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g23740 A02 12934660 G A missense_variant MODERATE c.1774C>T|p.Leu592Phe S146
2 BAA02g23740 A02 12934885 G A stop_gained HIGH c.1675C>T|p.Gln559* S132
S215
S89
3 BAA02g23740 A02 12935415 C T missense_variant MODERATE c.1349G>A|p.Arg450Lys S115
4 BAA02g23740 A02 12936132 C T missense_variant MODERATE c.908G>A|p.Arg303Gln S282
5 BAA02g23740 A02 12936719 C T missense_variant MODERATE c.509G>A|p.Ser170Asn S185
6 BAA02g23740 A02 12937300 G A missense_variant MODERATE c.256C>T|p.Leu86Phe S236
7 BAA02g23740 A02 12939444 C T upstream_gene_variant MODIFIER c.-1889G>A| S76
8 BAA02g23740 A02 12940004 C T upstream_gene_variant MODIFIER c.-2449G>A| S261
9 BAA02g23740 A02 12940483 G A upstream_gene_variant MODIFIER c.-2928C>T| S206
S26
10 BAA02g23740 A02 12940524 C T upstream_gene_variant MODIFIER c.-2969G>A| S268
11 BAA02g23740 A02 12941107 G A upstream_gene_variant MODIFIER c.-3552C>T| S184
12 BAA02g23740 A02 12941196 G A upstream_gene_variant MODIFIER c.-3641C>T| S156
13 BAA02g23740 A02 12942419 G A upstream_gene_variant MODIFIER c.-4864C>T| S57