NM_000256.3(MYBPC3):c.35T>C (p.Phe12Ser) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 3, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002487024.1
Allele description [Variation Report for NM_000256.3(MYBPC3):c.35T>C (p.Phe12Ser)]
NM_000256.3(MYBPC3):c.35T>C (p.Phe12Ser)
Condition(s)
Assertion and evidence details
Last Updated: Dec 24, 2023