NM_000492.4(CFTR):c.1052C>G (p.Thr351Ser) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 20, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002265581.10
Allele description [Variation Report for NM_000492.4(CFTR):c.1052C>G (p.Thr351Ser)]
NM_000492.4(CFTR):c.1052C>G (p.Thr351Ser)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
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Last Updated: Oct 26, 2024