NM_015662.3(IFT172):c.5024T>C (p.Val1675Ala) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 23, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001989586.11
Allele description [Variation Report for NM_015662.3(IFT172):c.5024T>C (p.Val1675Ala)]
NM_015662.3(IFT172):c.5024T>C (p.Val1675Ala)
Condition(s)
Assertion and evidence details
Last Updated: Jun 17, 2024