NM_015662.3(IFT172):c.666T>C (p.Tyr222=) AND not specified
- Germline classification:
- Benign (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001699874.2
Allele description [Variation Report for NM_015662.3(IFT172):c.666T>C (p.Tyr222=)]
NM_015662.3(IFT172):c.666T>C (p.Tyr222=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Dec 24, 2023