NM_003793.4(CTSF):c.1158C>T (p.Asn386=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Dec 11, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001613439.10
Allele description [Variation Report for NM_003793.4(CTSF):c.1158C>T (p.Asn386=)]
NM_003793.4(CTSF):c.1158C>T (p.Asn386=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Apr 20, 2024