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 BAA02g29760 A02 17086741 C T missense_variant MODERATE c.532G>A|p.Gly178Ser S183
S198
2 BAA02g29760 A02 17086764 G A missense_variant MODERATE c.509C>T|p.Ser170Phe S297
3 BAA02g29760 A02 17086780 G A missense_variant MODERATE c.493C>T|p.Leu165Phe S72
S78
4 BAA02g29760 A02 17086790 G A synonymous_variant LOW c.483C>T|p.Phe161Phe S133
5 BAA02g29760 A02 17087073 C T intron_variant MODIFIER c.230-30G>A| S54
6 BAA02g29760 A02 17087327 C T intron_variant MODIFIER c.230-284G>A| S53
7 BAA02g29760 A02 17087447 C T intron_variant MODIFIER c.229+202G>A| S203
8 BAA02g29760 A02 17088004 C T upstream_gene_variant MODIFIER c.-127G>A| S117
9 BAA02g29760 A02 17088359 G A upstream_gene_variant MODIFIER c.-482C>T| S50
10 BAA02g29760 A02 17088618 G A upstream_gene_variant MODIFIER c.-741C>T| S197
11 BAA02g29760 A02 17089854 G A upstream_gene_variant MODIFIER c.-1977C>T| S116
12 BAA02g29760 A02 17089897 C T upstream_gene_variant MODIFIER c.-2020G>A| S216
13 BAA02g29760 A02 17092032 G A upstream_gene_variant MODIFIER c.-4155C>T| S155
S211
14 BAA02g29760 A02 17092212 G A upstream_gene_variant MODIFIER c.-4335C>T| S291