NM_000602.5(SERPINE1):c.456G>C (p.Val152=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 4, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000900882.3
Allele description [Variation Report for NM_000602.5(SERPINE1):c.456G>C (p.Val152=)]
NM_000602.5(SERPINE1):c.456G>C (p.Val152=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Apr 9, 2023