NM_001365999.1(SZT2):c.7275T>C (p.Pro2425=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 10, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000234045.9
Allele description [Variation Report for NM_001365999.1(SZT2):c.7275T>C (p.Pro2425=)]
NM_001365999.1(SZT2):c.7275T>C (p.Pro2425=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 14, 2024