NM_005529.7(HSPG2):c.12982G>A (p.Ala4328Thr) AND not specified
- Germline classification:
- Benign/Likely benign (2 submissions)
- Last evaluated:
- Apr 10, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000324004.6
Allele description [Variation Report for NM_005529.7(HSPG2):c.12982G>A (p.Ala4328Thr)]
NM_005529.7(HSPG2):c.12982G>A (p.Ala4328Thr)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jul 7, 2024