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 BAA06g25750 A06 17650818 C T upstream_gene_variant MODIFIER c.-4455C>T| S202
2 BAA06g25750 A06 17652537 G A upstream_gene_variant MODIFIER c.-2736G>A| S213
3 BAA06g25750 A06 17652627 G A upstream_gene_variant MODIFIER c.-2646G>A| S284
4 BAA06g25750 A06 17652962 C T upstream_gene_variant MODIFIER c.-2311C>T| S280
5 BAA06g25750 A06 17653262 C T upstream_gene_variant MODIFIER c.-2011C>T| S182
6 BAA06g25750 A06 17653296 C T upstream_gene_variant MODIFIER c.-1977C>T| S295
7 BAA06g25750 A06 17654650 G A upstream_gene_variant MODIFIER c.-623G>A| S47
8 BAA06g25750 A06 17654771 C T upstream_gene_variant MODIFIER c.-502C>T| S284
9 BAA06g25750 A06 17655093 G A upstream_gene_variant MODIFIER c.-180G>A| S140
10 BAA06g25750 A06 17655762 C T intron_variant MODIFIER c.183+219C>T| S296
11 BAA06g25750 A06 17657750 G A synonymous_variant LOW c.285G>A|p.Lys95Lys S25
12 BAA06g25750 A06 17657762 C T synonymous_variant LOW c.297C>T|p.Cys99Cys S281
13 BAA06g25750 A06 17659266 G A missense_variant MODERATE c.935G>A|p.Cys312Tyr S170
14 BAA06g25750 A06 17659463 C T missense_variant MODERATE c.997C>T|p.His333Tyr S40
S49