NM_002095.6(GTF2E2):c.687C>T (p.Asp229=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 11, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002109269.5
Allele description [Variation Report for NM_002095.6(GTF2E2):c.687C>T (p.Asp229=)]
NM_002095.6(GTF2E2):c.687C>T (p.Asp229=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 5, 2024