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 BAA09g52940 A09 54425603 C T upstream_gene_variant MODIFIER c.-4592C>T| S219
S72
2 BAA09g52940 A09 54425680 C T upstream_gene_variant MODIFIER c.-4515C>T| S259
3 BAA09g52940 A09 54425741 C T upstream_gene_variant MODIFIER c.-4454C>T| S208
S93
4 BAA09g52940 A09 54426439 G A upstream_gene_variant MODIFIER c.-3756G>A| S144
5 BAA09g52940 A09 54427485 G A upstream_gene_variant MODIFIER c.-2710G>A| S148
S210
S31
6 BAA09g52940 A09 54427750 C T upstream_gene_variant MODIFIER c.-2445C>T| S153
7 BAA09g52940 A09 54428361 G A upstream_gene_variant MODIFIER c.-1834G>A| S165
8 BAA09g52940 A09 54429884 G A upstream_gene_variant MODIFIER c.-311G>A| S116
S181
9 BAA09g52940 A09 54429926 G A upstream_gene_variant MODIFIER c.-269G>A| S202
10 BAA09g52940 A09 54431311 C T missense_variant MODERATE c.1117C>T|p.Leu373Phe S78
S83
11 BAA09g52940 A09 54431880 G A synonymous_variant LOW c.1686G>A|p.Lys562Lys S209
12 BAA09g52940 A09 54431921 G A missense_variant MODERATE c.1727G>A|p.Gly576Glu S81
S85
13 BAA09g52940 A09 54431983 G A missense_variant MODERATE c.1789G>A|p.Gly597Ser S246
14 BAA09g52940 A09 54432423 G A stop_gained HIGH c.2229G>A|p.Trp743* S132
S137
S215
S89