NM_000492.4(CFTR):c.389T>C (p.Leu130Pro) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 9, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002261343.4
Allele description [Variation Report for NM_000492.4(CFTR):c.389T>C (p.Leu130Pro)]
NM_000492.4(CFTR):c.389T>C (p.Leu130Pro)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Jun 10, 2023