NM_018919.3(PCDHGA6):c.2206C>T (p.Pro736Ser) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 2, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004116119.1
Allele description [Variation Report for NM_018919.3(PCDHGA6):c.2206C>T (p.Pro736Ser)]
NM_018919.3(PCDHGA6):c.2206C>T (p.Pro736Ser)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 9, 2024