NM_018912.3(PCDHGA1):c.507C>G (p.Ser169Arg) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 3, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004310095.1
Allele description [Variation Report for NM_018912.3(PCDHGA1):c.507C>G (p.Ser169Arg)]
NM_018912.3(PCDHGA1):c.507C>G (p.Ser169Arg)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Nov 24, 2024