NM_018940.4(PCDHB7):c.922G>A (p.Asp308Asn) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 21, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004344459.1
Allele description [Variation Report for NM_018940.4(PCDHB7):c.922G>A (p.Asp308Asn)]
NM_018940.4(PCDHB7):c.922G>A (p.Asp308Asn)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 2, 2024