NM_015662.3(IFT172):c.899G>A (p.Arg300Gln) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 23, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001819939.4
Allele description [Variation Report for NM_015662.3(IFT172):c.899G>A (p.Arg300Gln)]
NM_015662.3(IFT172):c.899G>A (p.Arg300Gln)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 20, 2024