NM_001368120.1(PDLIM2):c.94G>T (p.Val32Leu) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 4, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004505388.1
Allele description [Variation Report for NM_001368120.1(PDLIM2):c.94G>T (p.Val32Leu)]
NM_001368120.1(PDLIM2):c.94G>T (p.Val32Leu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 7, 2024