NM_005529.7(HSPG2):c.12966C>T (p.Pro4322=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 14, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002603889.2
Allele description [Variation Report for NM_005529.7(HSPG2):c.12966C>T (p.Pro4322=)]
NM_005529.7(HSPG2):c.12966C>T (p.Pro4322=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 28, 2024