NM_001127898.4(CLCN5):c.1914C>T (p.Pro638=) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Sep 17, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000443529.1
Allele description [Variation Report for NM_001127898.4(CLCN5):c.1914C>T (p.Pro638=)]
NM_001127898.4(CLCN5):c.1914C>T (p.Pro638=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Feb 28, 2024