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 BAA02g09730 A02 4286719 C T missense_variant MODERATE c.3109G>A|p.Asp1037Asn S270
2 BAA02g09730 A02 4287168 C T missense_variant MODERATE c.2660G>A|p.Gly887Glu S63
3 BAA02g09730 A02 4287205 C T missense_variant MODERATE c.2623G>A|p.Gly875Ser S241
4 BAA02g09730 A02 4287685 G A missense_variant MODERATE c.2143C>T|p.His715Tyr S210
S225
5 BAA02g09730 A02 4288486 G A missense_variant MODERATE c.1342C>T|p.Pro448Ser S107
6 BAA02g09730 A02 4288619 C T synonymous_variant LOW c.1209G>A|p.Glu403Glu S40
S49
7 BAA02g09730 A02 4289695 G A synonymous_variant LOW c.664C>T|p.Leu222Leu S155
S211
8 BAA02g09730 A02 4289737 G A intron_variant MODIFIER c.645-23C>T| S291
9 BAA02g09730 A02 4290010 C T missense_variant MODERATE c.511G>A|p.Asp171Asn S272
10 BAA02g09730 A02 4290310 C T intron_variant MODIFIER c.313-16G>A| S183
S198
11 BAA02g09730 A02 4292875 G A upstream_gene_variant MODIFIER c.-1621C>T| S68
12 BAA02g09730 A02 4293481 G A upstream_gene_variant MODIFIER c.-2227C>T| S188
13 BAA02g09730 A02 4294805 C T upstream_gene_variant MODIFIER c.-3551G>A| S152
14 BAA02g09730 A02 4295607 C T upstream_gene_variant MODIFIER c.-4353G>A| S299