NM_000492.4(CFTR):c.743+40A>G AND not specified
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Dec 5, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000246696.16
Allele description [Variation Report for NM_000492.4(CFTR):c.743+40A>G]
NM_000492.4(CFTR):c.743+40A>G
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 1, 2024