NM_000492.4(CFTR):c.1853T>C (p.Ile618Thr) AND multiple conditions
- Germline classification:
- Likely pathogenic (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001004276.9
Allele description [Variation Report for NM_000492.4(CFTR):c.1853T>C (p.Ile618Thr)]
NM_000492.4(CFTR):c.1853T>C (p.Ile618Thr)
Condition(s)
Assertion and evidence details
Last Updated: Aug 18, 2024