NM_198253.3(TERT):c.2286C>T (p.His762=) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 5, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002530135.9
Allele description [Variation Report for NM_198253.3(TERT):c.2286C>T (p.His762=)]
NM_198253.3(TERT):c.2286C>T (p.His762=)
Condition(s)
Assertion and evidence details
Last Updated: Oct 13, 2024