NM_001365999.1(SZT2):c.4051T>C (p.Trp1351Arg) AND not provided
- Germline classification:
- Benign (3 submissions)
- Last evaluated:
- Jan 30, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000713745.19
Allele description [Variation Report for NM_001365999.1(SZT2):c.4051T>C (p.Trp1351Arg)]
NM_001365999.1(SZT2):c.4051T>C (p.Trp1351Arg)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Apr 20, 2024