NM_198253.3(TERT):c.2958T>C (p.Phe986=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 22, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003782128.1
Allele description [Variation Report for NM_198253.3(TERT):c.2958T>C (p.Phe986=)]
NM_198253.3(TERT):c.2958T>C (p.Phe986=)
Condition(s)
Assertion and evidence details
Last Updated: Mar 5, 2024