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 BAA09g43680 A09 49722657 G A upstream_gene_variant MODIFIER c.-4946G>A| S150
2 BAA09g43680 A09 49723397 G A upstream_gene_variant MODIFIER c.-4206G>A| S66
3 BAA09g43680 A09 49723852 G A upstream_gene_variant MODIFIER c.-3751G>A| S105
S106
4 BAA09g43680 A09 49724479 G A upstream_gene_variant MODIFIER c.-3124G>A| S203
5 BAA09g43680 A09 49724725 C T upstream_gene_variant MODIFIER c.-2878C>T| S251
6 BAA09g43680 A09 49725085 G A upstream_gene_variant MODIFIER c.-2518G>A| S190
7 BAA09g43680 A09 49725122 G A upstream_gene_variant MODIFIER c.-2481G>A| S271
8 BAA09g43680 A09 49725450 C T upstream_gene_variant MODIFIER c.-2153C>T| S40
S49
9 BAA09g43680 A09 49725544 C T upstream_gene_variant MODIFIER c.-2059C>T| S18
10 BAA09g43680 A09 49725841 G A upstream_gene_variant MODIFIER c.-1762G>A| S38
11 BAA09g43680 A09 49726868 G A upstream_gene_variant MODIFIER c.-735G>A| S149
12 BAA09g43680 A09 49727942 G A missense_variant MODERATE c.340G>A|p.Glu114Lys S126
13 BAA09g43680 A09 49727986 C T synonymous_variant LOW c.384C>T|p.Phe128Phe S25
S264
14 BAA09g43680 A09 49728516 C T missense_variant MODERATE c.914C>T|p.Ala305Val S120
15 BAA09g43680 A09 49729127 C T missense_variant MODERATE c.1525C>T|p.Leu509Phe S95