A22S (p.Ala22Ser) variant of TNNC1 (P63316)
A22S (p.Ala22Ser) in TNNC1 (P63316) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Dilated cardiomyopathy 1Z; Hypertrophic cardiomyopathy 13; Cardiovascular phenot. The record also includes published literature and structural context.
A22S (p.Ala22Ser) variant details
- p.Ala22Ser
- rs2471444722
- ClinGen CA353169634
- ClinVar RCV003448922
- ClinVar RCV004992609
- Uncertain significance
- Dilated cardiomyopathy 1Z; Hypertrophic cardiomyopathy 13; Cardiovascular phenot
- Missense
- ClinVar: Uncertain significance (Dilated cardiomyopathy 1Z; Hypertrophic cardiomyopathy 13; Cardi)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available
- Cited in: ACMG SF v3.1 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of… (PMID 35802134)
- Cited in: Clinical utility gene card for: hypertrophic cardiomyopathy (type 1-14). (PMID 21267010)