NM_015662.3(IFT172):c.1433A>T (p.Asn478Ile) AND multiple conditions
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 26, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001079162.8
Allele description [Variation Report for NM_015662.3(IFT172):c.1433A>T (p.Asn478Ile)]
NM_015662.3(IFT172):c.1433A>T (p.Asn478Ile)
Condition(s)
Assertion and evidence details
Last Updated: Dec 22, 2024