rs1234973794
- Uncertain significance
Your Genotype
Sign InDescription
This sequence change replaces threonine, which is neutral and polar, with isoleucine, which is neutral and non-polar, at codon 20 of the RNASEH2C protein (p.Thr20Ile). The frequency data for this variant in the population databases is considered unreliable, as metrics indicate poor data quality at this position in the gnomAD database. This variant has not been reported in the literature in individuals affected with RNASEH2C-related conditions. ClinVar contains an entry for this variant (Variation ID: 939310). Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Possibly Damaging"; Align-GVGD: "Class C0"). 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
G
Alternative Allele
A
Chromosome
11
Location
65720700
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_032193.4(RNASEH2C):c.59C>T (p.Thr20Ile)
Allele
A
Clinical Significance
Uncertain significance