NM_000546.6(TP53):c.993+227A>C AND not provided
- Germline classification:
- Uncertain significance (2 submissions)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001796025.5
Allele description [Variation Report for NM_000546.6(TP53):c.993+227A>C]
NM_000546.6(TP53):c.993+227A>C
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Dec 24, 2023