NM_001384732.1(CPLANE1):c.1173T>G (p.Ala391=) AND not provided
- Germline classification:
- Benign/Likely benign (3 submissions)
- Last evaluated:
- Jan 17, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000646716.14
Allele description [Variation Report for NM_001384732.1(CPLANE1):c.1173T>G (p.Ala391=)]
NM_001384732.1(CPLANE1):c.1173T>G (p.Ala391=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 5, 2024