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 BAA02g36500 A02 31225519 C T synonymous_variant LOW c.528G>A|p.Thr176Thr S167
2 BAA02g36500 A02 31225670 C T missense_variant MODERATE c.377G>A|p.Gly126Glu S301
S304
3 BAA02g36500 A02 31225686 G A missense_variant MODERATE c.361C>T|p.Leu121Phe S86
4 BAA02g36500 A02 31225757 G A missense_variant MODERATE c.290C>T|p.Pro97Leu S71
5 BAA02g36500 A02 31225764 C T missense_variant MODERATE c.283G>A|p.Gly95Ser S9
6 BAA02g36500 A02 31225796 G A missense_variant MODERATE c.251C>T|p.Ser84Leu S59
7 BAA02g36500 A02 31225877 G A missense_variant MODERATE c.170C>T|p.Ser57Phe S223
8 BAA02g36500 A02 31225894 G A synonymous_variant LOW c.153C>T|p.Leu51Leu S293
9 BAA02g36500 A02 31225907 G A missense_variant MODERATE c.140C>T|p.Ser47Phe S150
10 BAA02g36500 A02 31225959 G A stop_gained HIGH c.88C>T|p.Gln30* S245
11 BAA02g36500 A02 31225979 G A missense_variant MODERATE c.68C>T|p.Pro23Leu S134
12 BAA02g36500 A02 31228234 C T upstream_gene_variant MODIFIER c.-2188G>A| S167
13 BAA02g36500 A02 31228290 G A upstream_gene_variant MODIFIER c.-2244C>T| S50