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 BAA02g05910 A02 2512061 C T missense_variant MODERATE c.1381G>A|p.Gly461Ser S116
2 BAA02g05910 A02 2512112 G A synonymous_variant LOW c.1330C>T|p.Leu444Leu S132
S137
S215
3 BAA02g05910 A02 2512160 C T missense_variant MODERATE c.1282G>A|p.Gly428Arg S117
4 BAA02g05910 A02 2512243 G A missense_variant MODERATE c.1199C>T|p.Ser400Phe S132
S89
5 BAA02g05910 A02 2512380 G A synonymous_variant LOW c.1062C>T|p.Tyr354Tyr S7
6 BAA02g05910 A02 2512656 C T synonymous_variant LOW c.786G>A|p.Gln262Gln S185
7 BAA02g05910 A02 2512724 G A missense_variant MODERATE c.718C>T|p.Pro240Ser S266
8 BAA02g05910 A02 2513212 C T missense_variant MODERATE c.490G>A|p.Val164Ile S233
9 BAA02g05910 A02 2513405 G A synonymous_variant LOW c.297C>T|p.Asp99Asp S118
10 BAA02g05910 A02 2513830 C T synonymous_variant LOW c.60G>A|p.Ser20Ser S63
11 BAA02g05910 A02 2516327 C T upstream_gene_variant MODIFIER c.-2438G>A| S241
12 BAA02g05910 A02 2516671 C T upstream_gene_variant MODIFIER c.-2782G>A| S202
13 BAA02g05910 A02 2518851 C T upstream_gene_variant MODIFIER c.-4962G>A| S87