NM_005159.5(ACTC1):c.42C>T (p.Asn14=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 20, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000779684.2
Allele description [Variation Report for NM_005159.5(ACTC1):c.42C>T (p.Asn14=)]
NM_005159.5(ACTC1):c.42C>T (p.Asn14=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024