NM_001039958.2(MESP2):c.47G>A (p.Trp16Ter) AND not provided
- Germline classification:
- Pathogenic (1 submission)
- Last evaluated:
- Nov 7, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001941341.3
Allele description [Variation Report for NM_001039958.2(MESP2):c.47G>A (p.Trp16Ter)]
NM_001039958.2(MESP2):c.47G>A (p.Trp16Ter)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024