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 BAA09g62080 A09 58758933 C T downstream_gene_variant MODIFIER c.*4313G>A| S221
2 BAA09g62080 A09 58758936 G A downstream_gene_variant MODIFIER c.*4310C>T| S103
3 BAA09g62080 A09 58761691 G A downstream_gene_variant MODIFIER c.*1555C>T| S288
4 BAA09g62080 A09 58763963 C T missense_variant MODERATE c.1063G>A|p.Glu355Lys S236
5 BAA09g62080 A09 58764235 C T missense_variant MODERATE c.791G>A|p.Gly264Glu S259
6 BAA09g62080 A09 58764335 G A missense_variant MODERATE c.691C>T|p.Pro231Ser S295
7 BAA09g62080 A09 58766432 C T upstream_gene_variant MODIFIER c.-1407G>A| S56
8 BAA09g62080 A09 58766973 G A upstream_gene_variant MODIFIER c.-1948C>T| S148
S210
S30
S31
9 BAA09g62080 A09 58767537 C T upstream_gene_variant MODIFIER c.-2512G>A| S205
10 BAA09g62080 A09 58767927 G A upstream_gene_variant MODIFIER c.-2902C>T| S8
11 BAA09g62080 A09 58768171 G A upstream_gene_variant MODIFIER c.-3146C>T| S69
12 BAA09g62080 A09 58768340 G A upstream_gene_variant MODIFIER c.-3315C>T| S246
13 BAA09g62080 A09 58769489 G A upstream_gene_variant MODIFIER c.-4464C>T| S47