NM_000614.4(CNTF):c.565C>T (p.Arg189Cys) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 1, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003395810.9
Allele description [Variation Report for NM_000614.4(CNTF):c.565C>T (p.Arg189Cys)]
NM_000614.4(CNTF):c.565C>T (p.Arg189Cys)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 8, 2024