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


Gene ID

Results: 1 - 14 of 14 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g29060 A02 16566226 C T downstream_gene_variant MODIFIER c.*1212G>A| S234
S255
2 BAA02g29060 A02 16566539 G A downstream_gene_variant MODIFIER c.*899C>T| S208
3 BAA02g29060 A02 16567914 G A intron_variant MODIFIER c.802-21C>T| S196
4 BAA02g29060 A02 16567931 G A intron_variant MODIFIER c.802-38C>T| S298
5 BAA02g29060 A02 16568157 G A synonymous_variant LOW c.627C>T|p.Leu209Leu S289
S290
6 BAA02g29060 A02 16568441 G A missense_variant MODERATE c.407C>T|p.Ser136Phe S128
7 BAA02g29060 A02 16569254 C T upstream_gene_variant MODIFIER c.-332G>A| S131
8 BAA02g29060 A02 16570059 C T upstream_gene_variant MODIFIER c.-1137G>A| S84
S93
9 BAA02g29060 A02 16570397 G T upstream_gene_variant MODIFIER c.-1475C>A| S72
S78
10 BAA02g29060 A02 16570484 G A upstream_gene_variant MODIFIER c.-1562C>T| S132
S137
S215
11 BAA02g29060 A02 16570734 G A upstream_gene_variant MODIFIER c.-1812C>T| S37
12 BAA02g29060 A02 16571032 G A upstream_gene_variant MODIFIER c.-2110C>T| S4
13 BAA02g29060 A02 16571067 C T upstream_gene_variant MODIFIER c.-2145G>A| S130
14 BAA02g29060 A02 16572935 C T upstream_gene_variant MODIFIER c.-4013G>A| S270