NM_014714.4(IFT140):c.3711C>T (p.Phe1237=) AND not specified
- Germline classification:
- Likely benign (3 submissions)
- Last evaluated:
- Mar 14, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000733940.9
Allele description [Variation Report for NM_014714.4(IFT140):c.3711C>T (p.Phe1237=)]
NM_014714.4(IFT140):c.3711C>T (p.Phe1237=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Apr 15, 2024