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 BAA09g45560 A09 50742208 C T upstream_gene_variant MODIFIER c.-4531C>T| S296
2 BAA09g45560 A09 50742469 G A upstream_gene_variant MODIFIER c.-4270G>A| S164
3 BAA09g45560 A09 50742568 C T upstream_gene_variant MODIFIER c.-4171C>T| S183
4 BAA09g45560 A09 50743692 G A upstream_gene_variant MODIFIER c.-3047G>A| S167
5 BAA09g45560 A09 50744203 C T upstream_gene_variant MODIFIER c.-2536C>T| S30
S31
6 BAA09g45560 A09 50746112 G A upstream_gene_variant MODIFIER c.-627G>A| S86
7 BAA09g45560 A09 50746237 C T upstream_gene_variant MODIFIER c.-502C>T| S241
8 BAA09g45560 A09 50746444 G A upstream_gene_variant MODIFIER c.-295G>A| S143
9 BAA09g45560 A09 50746582 G A upstream_gene_variant MODIFIER c.-157G>A| S13
10 BAA09g45560 A09 50746840 C T synonymous_variant LOW c.102C>T|p.Ser34Ser S297
11 BAA09g45560 A09 50746874 G A missense_variant MODERATE c.136G>A|p.Asp46Asn S88
12 BAA09g45560 A09 50747067 G A missense_variant MODERATE c.329G>A|p.Arg110Lys S2
13 BAA09g45560 A09 50747586 C T intron_variant MODIFIER c.434-89C>T| S67
14 BAA09g45560 A09 50747630 C T intron_variant MODIFIER c.434-45C>T| S57
15 BAA09g45560 A09 50750347 G A downstream_gene_variant MODIFIER c.*472G>A| S78