NM_000492.4(CFTR):c.1311T>C (p.Gly437=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 28, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000780174.2
Allele description [Variation Report for NM_000492.4(CFTR):c.1311T>C (p.Gly437=)]
NM_000492.4(CFTR):c.1311T>C (p.Gly437=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
D site-binding protein isoform 1 [Rattus norvegicus]
D site-binding protein isoform 1 [Rattus norvegicus]gi|7549756|ref|NP_036675.1|Protein
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Last Updated: Sep 29, 2024