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 BAA02g40980 A02 34384080 C T synonymous_variant LOW c.522C>T|p.His174His S162
2 BAA02g40980 A02 34384377 C T synonymous_variant LOW c.819C>T|p.Thr273Thr S128
3 BAA02g40980 A02 34384894 G A missense_variant MODERATE c.1336G>A|p.Asp446Asn S199
4 BAA02g40980 A02 34385243 G A missense_variant MODERATE c.1685G>A|p.Ser562Asn S35
5 BAA02g40980 A02 34385283 G A synonymous_variant LOW c.1725G>A|p.Lys575Lys S269
6 BAA02g40980 A02 34385295 C T synonymous_variant LOW c.1737C>T|p.Val579Val S54
7 BAA02g40980 A02 34385486 C T synonymous_variant LOW c.1845C>T|p.Ser615Ser S249
8 BAA02g40980 A02 34385862 C T synonymous_variant LOW c.2221C>T|p.Leu741Leu S120
9 BAA02g40980 A02 34385914 C T missense_variant MODERATE c.2273C>T|p.Pro758Leu S121
10 BAA02g40980 A02 34385961 C T stop_gained HIGH c.2320C>T|p.Gln774* S53
11 BAA02g40980 A02 34386143 C T synonymous_variant LOW c.2502C>T|p.Ile834Ile S259
12 BAA02g40980 A02 34387071 C T downstream_gene_variant MODIFIER c.*664C>T| S171
13 BAA02g40980 A02 34387124 C T downstream_gene_variant MODIFIER c.*717C>T| S118