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


Gene ID

Results: 1 - 13 of 13 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA03g43860 A03 20800457 G A missense_variant MODERATE c.202G>A|p.Asp68Asn S162
2 BAA03g43860 A03 20801533 G A missense_variant MODERATE c.886G>A|p.Asp296Asn S171
3 BAA03g43860 A03 20801552 C T missense_variant MODERATE c.905C>T|p.Ser302Phe S231
4 BAA03g43860 A03 20801777 G A missense_variant&splice_region_variant MODERATE c.937G>A|p.Glu313Lys S289
S290
5 BAA03g43860 A03 20801813 G A missense_variant MODERATE c.973G>A|p.Val325Ile S272
6 BAA03g43860 A03 20802318 C T synonymous_variant LOW c.1248C>T|p.Ser416Ser S208
7 BAA03g43860 A03 20803512 G A missense_variant MODERATE c.1897G>A|p.Gly633Ser S54
8 BAA03g43860 A03 20804147 C T downstream_gene_variant MODIFIER c.*165C>T| S96
9 BAA03g43860 A03 20804247 A T downstream_gene_variant MODIFIER c.*265A>T| S6
10 BAA03g43860 A03 20804892 G A downstream_gene_variant MODIFIER c.*910G>A| S275
11 BAA03g43860 A03 20805515 C T downstream_gene_variant MODIFIER c.*1533C>T| S127
12 BAA03g43860 A03 20806053 G A downstream_gene_variant MODIFIER c.*2071G>A| S68
13 BAA03g43860 A03 20808338 C T downstream_gene_variant MODIFIER c.*4356C>T| S53