NM_031246.4(PSG2):c.58G>C (p.Val20Leu) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Dec 31, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000947964.4
Allele description [Variation Report for NM_031246.4(PSG2):c.58G>C (p.Val20Leu)]
NM_031246.4(PSG2):c.58G>C (p.Val20Leu)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Dec 24, 2023