NM_000256.3(MYBPC3):c.3315C>T (p.Ala1105=) AND not specified
- Germline classification:
- Benign/Likely benign (2 submissions)
- Last evaluated:
- Jun 28, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000155644.6
Allele description [Variation Report for NM_000256.3(MYBPC3):c.3315C>T (p.Ala1105=)]
NM_000256.3(MYBPC3):c.3315C>T (p.Ala1105=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024