NM_001002295.2(GATA3):c.216G>T (p.Val72=) AND not provided
- Germline classification:
- Benign/Likely benign (3 submissions)
- Last evaluated:
- Jan 7, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001549549.13
Allele description [Variation Report for NM_001002295.2(GATA3):c.216G>T (p.Val72=)]
NM_001002295.2(GATA3):c.216G>T (p.Val72=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 19, 2024