rs200684841
- Uncertain significance
Your Genotype
Sign InDescription
This sequence change replaces glutamic acid, which is acidic and polar, with lysine, which is basic and polar, at codon 807 of the TRPM1 protein (p.Glu807Lys). This variant is present in population databases (rs200684841, gnomAD 0.07%). This variant has not been reported in the literature in individuals affected with TRPM1-related conditions. ClinVar contains an entry for this variant (Variation ID: 194944). Algorithms developed to predict the effect of missense changes on protein structure and function (SIFT, PolyPhen-2, Align-GVGD) all suggest that this variant is likely to be tolerated. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance.
Reference Allele
C
Alternative Allele
T
Chromosome
15
Location
31037797
Variant Type
SNP
Genes
LOC105370752
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.2485G>A (p.Glu829Lys)
Allele
T
Clinical Significance
Uncertain significance