rs141449031
- Benign/Likely benign
- Uncertain significance
Your Genotype
Sign InDescription
This alteration is classified as likely benign based on a combination of the following: population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.
Reference Allele
C
Alternative Allele
G
T
Chromosome
16
Location
2088451
Variant Type
SNP
ClinVar
Name
NM_000548.5(TSC2):c.5265C>T (p.Cys1755=)
Allele
T
Clinical Significance
Benign/Likely benign
Name
NM_000548.5(TSC2):c.5265C>G (p.Cys1755Trp)
Allele
G
Clinical Significance
Uncertain significance