NM_001143992.2(WRAP53):c.18_19del (p.Gln7fs) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 6, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001856160.4
Allele description [Variation Report for NM_001143992.2(WRAP53):c.18_19del (p.Gln7fs)]
NM_001143992.2(WRAP53):c.18_19del (p.Gln7fs)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024