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 BAA02g32070 A02 26263709 C T upstream_gene_variant MODIFIER c.-1628C>T| S235
2 BAA02g32070 A02 26265397 G A missense_variant MODERATE c.61G>A|p.Asp21Asn S2
3 BAA02g32070 A02 26266015 C T intron_variant MODIFIER c.242+437C>T| S148
S210
S30
S31
4 BAA02g32070 A02 26267713 G A intron_variant MODIFIER c.243-1414G>A| S135
5 BAA02g32070 A02 26268256 G A intron_variant MODIFIER c.243-871G>A| S130
6 BAA02g32070 A02 26269197 C T missense_variant MODERATE c.313C>T|p.Arg105Cys S56
7 BAA02g32070 A02 26269307 G A intron_variant MODIFIER c.339+84G>A| S283
8 BAA02g32070 A02 26269373 C T intron_variant MODIFIER c.339+150C>T| S251
9 BAA02g32070 A02 26270461 C T synonymous_variant LOW c.564C>T|p.Asp188Asp S94
10 BAA02g32070 A02 26271330 G A missense_variant MODERATE c.1294G>A|p.Glu432Lys S83
S88
11 BAA02g32070 A02 26271390 G A missense_variant MODERATE c.1354G>A|p.Asp452Asn S303
12 BAA02g32070 A02 26271492 G A missense_variant MODERATE c.1456G>A|p.Asp486Asn S15
13 BAA02g32070 A02 26272575 C T downstream_gene_variant MODIFIER c.*997C>T| S37