NM_152383.5(DIS3L2):c.36C>G (p.Pro12=) AND Perlman syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 29, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001454947.6
Allele description [Variation Report for NM_152383.5(DIS3L2):c.36C>G (p.Pro12=)]
NM_152383.5(DIS3L2):c.36C>G (p.Pro12=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 28, 2024