NM_000492.4(CFTR):c.2981T>G (p.Phe994Cys) AND not specified
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Mar 29, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000855590.9
Allele description [Variation Report for NM_000492.4(CFTR):c.2981T>G (p.Phe994Cys)]
NM_000492.4(CFTR):c.2981T>G (p.Phe994Cys)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024