NM_015662.3(IFT172):c.1433A>T (p.Asn478Ile) AND not provided
- Germline classification:
- Benign/Likely benign (5 submissions)
- Last evaluated:
- Jan 1, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000840691.18
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)
- Synonyms:
- none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Dec 22, 2024