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 BAA09g36750 A09 44969227 C T upstream_gene_variant MODIFIER c.-4835C>T| S66
2 BAA09g36750 A09 44969287 C T upstream_gene_variant MODIFIER c.-4775C>T| S142
3 BAA09g36750 A09 44972325 G A upstream_gene_variant MODIFIER c.-1737G>A| S107
S236
4 BAA09g36750 A09 44972661 C T upstream_gene_variant MODIFIER c.-1401C>T| S64
5 BAA09g36750 A09 44974605 C T missense_variant MODERATE c.469C>T|p.Pro157Ser S305
6 BAA09g36750 A09 44975240 C T missense_variant MODERATE c.847C>T|p.His283Tyr S121
7 BAA09g36750 A09 44975264 G A missense_variant MODERATE c.871G>A|p.Glu291Lys S84
S93
8 BAA09g36750 A09 44975482 G A missense_variant MODERATE c.1021G>A|p.Asp341Asn S161
9 BAA09g36750 A09 44975643 C T missense_variant MODERATE c.1112C>T|p.Pro371Leu S125
10 BAA09g36750 A09 44976368 C T missense_variant MODERATE c.1837C>T|p.Arg613Cys S183
S198
11 BAA09g36750 A09 44976592 G A synonymous_variant LOW c.1971G>A|p.Lys657Lys S176
12 BAA09g36750 A09 44976646 C T synonymous_variant LOW c.2025C>T|p.Tyr675Tyr S131
13 BAA09g36750 A09 44977047 C T missense_variant MODERATE c.2269C>T|p.Pro757Ser S68
14 BAA09g36750 A09 44978591 G A downstream_gene_variant MODIFIER c.*1325G>A| S197
15 BAA09g36750 A09 44979646 G A downstream_gene_variant MODIFIER c.*2380G>A| S217
16 BAA09g36750 A09 44980916 C T downstream_gene_variant MODIFIER c.*3650C>T| S180