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


Gene ID

Results: 1 - 16 of 16 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g43460 A02 35996769 G A upstream_gene_variant MODIFIER c.-4868G>A| S28
2 BAA02g43460 A02 35997089 C T upstream_gene_variant MODIFIER c.-4548C>T| S132
S137
S215
3 BAA02g43460 A02 35999230 G A upstream_gene_variant MODIFIER c.-2407G>A| S2
4 BAA02g43460 A02 36000046 C T upstream_gene_variant MODIFIER c.-1591C>T| S192
5 BAA02g43460 A02 36000073 A G upstream_gene_variant MODIFIER c.-1564A>G| S63
6 BAA02g43460 A02 36000081 C T upstream_gene_variant MODIFIER c.-1556C>T| S63
7 BAA02g43460 A02 36000366 G A upstream_gene_variant MODIFIER c.-1271G>A| S292
8 BAA02g43460 A02 36000838 C T upstream_gene_variant MODIFIER c.-799C>T| S257
9 BAA02g43460 A02 36000940 G A upstream_gene_variant MODIFIER c.-697G>A| S41
10 BAA02g43460 A02 36000944 C T upstream_gene_variant MODIFIER c.-693C>T| S66
11 BAA02g43460 A02 36000980 C T upstream_gene_variant MODIFIER c.-657C>T| S263
12 BAA02g43460 A02 36001352 C T upstream_gene_variant MODIFIER c.-285C>T| S295
13 BAA02g43460 A02 36001830 G A missense_variant MODERATE c.194G>A|p.Arg65Lys S188
14 BAA02g43460 A02 36002410 G A missense_variant MODERATE c.774G>A|p.Met258Ile S251
15 BAA02g43460 A02 36002471 C T stop_gained HIGH c.835C>T|p.Gln279* S58
16 BAA02g43460 A02 36002549 C T synonymous_variant LOW c.913C>T|p.Leu305Leu S271