NM_198253.3(TERT):c.1932G>A (p.Thr644=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 23, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001821374.11
Allele description [Variation Report for NM_198253.3(TERT):c.1932G>A (p.Thr644=)]
NM_198253.3(TERT):c.1932G>A (p.Thr644=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jul 29, 2024