NM_000492.4(CFTR):c.2736G>C (p.Ser912=) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 22, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000728887.8
Allele description [Variation Report for NM_000492.4(CFTR):c.2736G>C (p.Ser912=)]
NM_000492.4(CFTR):c.2736G>C (p.Ser912=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 1, 2024