NM_000257.4(MYH7):c.2692C>T (p.Leu898=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 7, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000602384.8
Allele description [Variation Report for NM_000257.4(MYH7):c.2692C>T (p.Leu898=)]
NM_000257.4(MYH7):c.2692C>T (p.Leu898=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Apr 20, 2024