NM_015662.3(IFT172):c.1523G>A (p.Arg508His) AND multiple conditions
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Oct 24, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001053472.7
Allele description [Variation Report for NM_015662.3(IFT172):c.1523G>A (p.Arg508His)]
NM_015662.3(IFT172):c.1523G>A (p.Arg508His)
Condition(s)
Assertion and evidence details
Last Updated: Feb 1, 2025