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


Gene ID

Results: 1 - 17 of 17 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA01g15820 A01 7685856 C T upstream_gene_variant MODIFIER c.-4943C>T| S210
S225
2 BAA01g15820 A01 7687633 G A upstream_gene_variant MODIFIER c.-3166G>A| S129
3 BAA01g15820 A01 7687931 C T upstream_gene_variant MODIFIER c.-2868C>T| S164
4 BAA01g15820 A01 7688088 G A upstream_gene_variant MODIFIER c.-2711G>A| S40
5 BAA01g15820 A01 7688762 G A upstream_gene_variant MODIFIER c.-2037G>A| S249
6 BAA01g15820 A01 7689688 G A upstream_gene_variant MODIFIER c.-1111G>A| S199
7 BAA01g15820 A01 7690084 G A upstream_gene_variant MODIFIER c.-715G>A| S72
S78
8 BAA01g15820 A01 7690135 G A upstream_gene_variant MODIFIER c.-664G>A| S240
9 BAA01g15820 A01 7690197 C T upstream_gene_variant MODIFIER c.-602C>T| S185
10 BAA01g15820 A01 7690956 A T missense_variant MODERATE c.158A>T|p.Gln53Leu S143
11 BAA01g15820 A01 7690987 C T synonymous_variant LOW c.189C>T|p.Arg63Arg S128
12 BAA01g15820 A01 7691009 C T missense_variant MODERATE c.211C>T|p.Pro71Ser S182
13 BAA01g15820 A01 7691056 G A intron_variant MODIFIER c.244+14G>A| S129
14 BAA01g15820 A01 7691178 C T synonymous_variant LOW c.324C>T|p.Arg108Arg S182
15 BAA01g15820 A01 7691275 G A missense_variant MODERATE c.421G>A|p.Val141Ile S117
16 BAA01g15820 A01 7691640 G A synonymous_variant LOW c.618G>A|p.Arg206Arg S92
17 BAA01g15820 A01 7691899 G A missense_variant MODERATE c.793G>A|p.Val265Ile S306
S308