NM_001018005.2(TPM1):c.842T>C (p.Met281Thr) AND Primary familial hypertrophic cardiomyopathy
- Germline classification:
- Likely pathogenic (1 submission)
- Last evaluated:
- Jul 7, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000622737.4
Allele description [Variation Report for NM_001018005.2(TPM1):c.842T>C (p.Met281Thr)]
NM_001018005.2(TPM1):c.842T>C (p.Met281Thr)
Condition(s)
Assertion and evidence details
Last Updated: May 1, 2024