NM_000492.4(CFTR):c.1310G>A (p.Gly437Asp) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 9, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001283963.1
Allele description [Variation Report for NM_000492.4(CFTR):c.1310G>A (p.Gly437Asp)]
NM_000492.4(CFTR):c.1310G>A (p.Gly437Asp)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024