NM_001365999.1(SZT2):c.8547C>T (p.Tyr2849=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 12, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000902833.6
Allele description [Variation Report for NM_001365999.1(SZT2):c.8547C>T (p.Tyr2849=)]
NM_001365999.1(SZT2):c.8547C>T (p.Tyr2849=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 14, 2024