NM_198253.3(TERT):c.1068C>T (p.Gly356=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 5, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002530092.9
Allele description [Variation Report for NM_198253.3(TERT):c.1068C>T (p.Gly356=)]
NM_198253.3(TERT):c.1068C>T (p.Gly356=)
Condition(s)
-
GDS3355[ACCN] AND gsm[ETYP] (8)
GEO DataSets
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See more...Assertion and evidence details
Last Updated: Sep 16, 2024