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 BAA02g36640 A02 31377095 G A upstream_gene_variant MODIFIER c.-4856G>A| S177
2 BAA02g36640 A02 31381834 G A upstream_gene_variant MODIFIER c.-117G>A| S238
3 BAA02g36640 A02 31382204 C T synonymous_variant LOW c.183C>T|p.Asp61Asp S257
4 BAA02g36640 A02 31382325 G A intron_variant MODIFIER c.234-19G>A| S142
5 BAA02g36640 A02 31382600 G A synonymous_variant LOW c.414G>A|p.Lys138Lys S62
6 BAA02g36640 A02 31382647 G A splice_region_variant&intron_variant LOW c.456+5G>A| S136
7 BAA02g36640 A02 31383098 G A missense_variant MODERATE c.682G>A|p.Val228Ile S155
S211
8 BAA02g36640 A02 31383403 C T missense_variant MODERATE c.803C>T|p.Ser268Phe S46
9 BAA02g36640 A02 31384935 G A missense_variant MODERATE c.1529G>A|p.Gly510Glu S111
10 BAA02g36640 A02 31385216 G A splice_donor_variant&intron_variant HIGH c.1710+1G>A| S247
11 BAA02g36640 A02 31386680 C T synonymous_variant LOW c.2415C>T|p.Tyr805Tyr S15
S3
12 BAA02g36640 A02 31387091 T A missense_variant MODERATE c.2657T>A|p.Ile886Lys S291
13 BAA02g36640 A02 31387613 C T downstream_gene_variant MODIFIER c.*130C>T| S219
S72
14 BAA02g36640 A02 31388743 C T downstream_gene_variant MODIFIER c.*1260C>T| S299
15 BAA02g36640 A02 31389170 G A downstream_gene_variant MODIFIER c.*1687G>A| S188