NM_000492.4(CFTR):c.169T>G (p.Trp57Gly) AND not provided
- Germline classification:
- Pathogenic (1 submission)
- Last evaluated:
- Sep 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003114230.10
Allele description [Variation Report for NM_000492.4(CFTR):c.169T>G (p.Trp57Gly)]
NM_000492.4(CFTR):c.169T>G (p.Trp57Gly)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 13, 2024