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


Gene ID

Results: 1 - 16 of 16 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g20380 A09 12577838 T A upstream_gene_variant MODIFIER c.-4989T>A| S213
2 BAA09g20380 A09 12578195 C T upstream_gene_variant MODIFIER c.-4632C>T| S53
3 BAA09g20380 A09 12578220 C T upstream_gene_variant MODIFIER c.-4607C>T| S204
4 BAA09g20380 A09 12578265 G A upstream_gene_variant MODIFIER c.-4562G>A| S19
5 BAA09g20380 A09 12578775 C T upstream_gene_variant MODIFIER c.-4052C>T| S234
S236
6 BAA09g20380 A09 12578916 C T upstream_gene_variant MODIFIER c.-3911C>T| S104
S52
7 BAA09g20380 A09 12579170 G A upstream_gene_variant MODIFIER c.-3657G>A| S149
8 BAA09g20380 A09 12579212 C T upstream_gene_variant MODIFIER c.-3615C>T| S223
9 BAA09g20380 A09 12581691 C T upstream_gene_variant MODIFIER c.-1136C>T| S60
10 BAA09g20380 A09 12581745 C T upstream_gene_variant MODIFIER c.-1082C>T| S255
11 BAA09g20380 A09 12582293 G A upstream_gene_variant MODIFIER c.-534G>A| S239
S33
12 BAA09g20380 A09 12582970 G A synonymous_variant LOW c.144G>A|p.Glu48Glu S274
13 BAA09g20380 A09 12583419 G A missense_variant MODERATE c.524G>A|p.Arg175Gln S199
14 BAA09g20380 A09 12583463 C T stop_gained HIGH c.568C>T|p.Arg190* S156
15 BAA09g20380 A09 12587461 C T downstream_gene_variant MODIFIER c.*2260C>T| S50
16 BAA09g20380 A09 12588149 G A downstream_gene_variant MODIFIER c.*2948G>A| S180