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


Gene ID

Results: 1 - 20 of 20 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g27180 A09 17771575 C T upstream_gene_variant MODIFIER c.-3624C>T| S270
2 BAA09g27180 A09 17771816 C T upstream_gene_variant MODIFIER c.-3383C>T| S30
S31
3 BAA09g27180 A09 17771936 G A upstream_gene_variant MODIFIER c.-3263G>A| S204
4 BAA09g27180 A09 17771963 G A upstream_gene_variant MODIFIER c.-3236G>A| S198
5 BAA09g27180 A09 17772330 G A upstream_gene_variant MODIFIER c.-2869G>A| S162
6 BAA09g27180 A09 17773069 G A upstream_gene_variant MODIFIER c.-2130G>A| S249
7 BAA09g27180 A09 17773631 A G upstream_gene_variant MODIFIER c.-1568A>G| S71
8 BAA09g27180 A09 17773763 G A upstream_gene_variant MODIFIER c.-1436G>A| S203
9 BAA09g27180 A09 17773934 G A upstream_gene_variant MODIFIER c.-1265G>A| S267
10 BAA09g27180 A09 17773984 C T upstream_gene_variant MODIFIER c.-1215C>T| S238
11 BAA09g27180 A09 17775297 C T synonymous_variant LOW c.99C>T|p.Leu33Leu S272
12 BAA09g27180 A09 17775450 C T synonymous_variant LOW c.252C>T|p.Val84Val S15
S3
13 BAA09g27180 A09 17775835 C T missense_variant MODERATE c.637C>T|p.Pro213Ser S221
14 BAA09g27180 A09 17775836 C T missense_variant MODERATE c.638C>T|p.Pro213Leu S234
15 BAA09g27180 A09 17776014 G A synonymous_variant LOW c.816G>A|p.Leu272Leu S224
16 BAA09g27180 A09 17776027 G A missense_variant MODERATE c.829G>A|p.Val277Ile S210
S225
17 BAA09g27180 A09 17776366 G A missense_variant MODERATE c.1168G>A|p.Val390Ile S281
18 BAA09g27180 A09 17776561 C T downstream_gene_variant MODIFIER c.*52C>T| S94
19 BAA09g27180 A09 17776649 G A downstream_gene_variant MODIFIER c.*140G>A| S18
20 BAA09g27180 A09 17776998 C T downstream_gene_variant MODIFIER c.*489C>T| S62