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


Gene ID

Results: 1 - 15 of 15 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA03g47660 A03 22882705 C T missense_variant MODERATE c.442C>T|p.Pro148Ser S117
2 BAA03g47660 A03 22882717 G A missense_variant MODERATE c.454G>A|p.Asp152Asn S260
3 BAA03g47660 A03 22883178 G A synonymous_variant LOW c.915G>A|p.Arg305Arg S302
4 BAA03g47660 A03 22884635 G A missense_variant MODERATE c.1847G>A|p.Cys616Tyr S302
5 BAA03g47660 A03 22885293 C T missense_variant MODERATE c.2287C>T|p.Pro763Ser S126
6 BAA03g47660 A03 22885632 C T missense_variant MODERATE c.2626C>T|p.Pro876Ser S240
7 BAA03g47660 A03 22886112 C T missense_variant MODERATE c.3106C>T|p.Pro1036Ser S207
8 BAA03g47660 A03 22887680 G A synonymous_variant LOW c.4473G>A|p.Pro1491Pro S51
9 BAA03g47660 A03 22888036 C T missense_variant MODERATE c.4829C>T|p.Ala1610Val S79
S91
10 BAA03g47660 A03 22888719 G A missense_variant MODERATE c.5512G>A|p.Asp1838Asn S80
11 BAA03g47660 A03 22890926 C T downstream_gene_variant MODIFIER c.*2004C>T| S184
12 BAA03g47660 A03 22891120 G A downstream_gene_variant MODIFIER c.*2198G>A| S31
13 BAA03g47660 A03 22891701 G A downstream_gene_variant MODIFIER c.*2779G>A| S9
14 BAA03g47660 A03 22892279 C T downstream_gene_variant MODIFIER c.*3357C>T| S69
15 BAA03g47660 A03 22892304 G A downstream_gene_variant MODIFIER c.*3382G>A| S262