NM_005529.7(HSPG2):c.13137C>T (p.Arg4379=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 16, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000882229.6
Allele description [Variation Report for NM_005529.7(HSPG2):c.13137C>T (p.Arg4379=)]
NM_005529.7(HSPG2):c.13137C>T (p.Arg4379=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024