NM_000492.4(CFTR):c.3080T>C (p.Ile1027Thr) AND not specified
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Dec 18, 2012
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000078993.25
Allele description [Variation Report for NM_000492.4(CFTR):c.3080T>C (p.Ile1027Thr)]
NM_000492.4(CFTR):c.3080T>C (p.Ile1027Thr)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 1, 2024