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


Gene ID

Results: 1 - 14 of 14 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g38710 A09 46460486 G A upstream_gene_variant MODIFIER c.-4684G>A| S13
2 BAA09g38710 A09 46462622 G A upstream_gene_variant MODIFIER c.-2548G>A| S130
3 BAA09g38710 A09 46465213 G A missense_variant MODERATE c.44G>A|p.Arg15Lys S12
4 BAA09g38710 A09 46465220 C T synonymous_variant LOW c.51C>T|p.Asn17Asn S206
S26
5 BAA09g38710 A09 46465853 G A downstream_gene_variant MODIFIER c.*16G>A| S262
6 BAA09g38710 A09 46465865 G A downstream_gene_variant MODIFIER c.*28G>A| S25
7 BAA09g38710 A09 46466422 G A downstream_gene_variant MODIFIER c.*585G>A| S162
8 BAA09g38710 A09 46466795 G A downstream_gene_variant MODIFIER c.*958G>A| S175
9 BAA09g38710 A09 46467299 C T downstream_gene_variant MODIFIER c.*1462C>T| S224
10 BAA09g38710 A09 46467370 C T downstream_gene_variant MODIFIER c.*1533C>T| S192
11 BAA09g38710 A09 46468731 G A downstream_gene_variant MODIFIER c.*2894G>A| S67
12 BAA09g38710 A09 46468947 G A downstream_gene_variant MODIFIER c.*3110G>A| S143
13 BAA09g38710 A09 46469688 C T downstream_gene_variant MODIFIER c.*3851C>T| S124
14 BAA09g38710 A09 46470796 C T downstream_gene_variant MODIFIER c.*4959C>T| S302