NM_001012759.3(CTU2):c.522C>T (p.Tyr174=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 12, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000949817.7
Allele description [Variation Report for NM_001012759.3(CTU2):c.522C>T (p.Tyr174=)]
NM_001012759.3(CTU2):c.522C>T (p.Tyr174=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 26, 2024