NM_000256.3(MYBPC3):c.1149G>T (p.Leu383=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 28, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000611361.1
Allele description [Variation Report for NM_000256.3(MYBPC3):c.1149G>T (p.Leu383=)]
NM_000256.3(MYBPC3):c.1149G>T (p.Leu383=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 1, 2024