NM_198253.3(TERT):c.1026G>C (p.Arg342=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 31, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003053436.10
Allele description [Variation Report for NM_198253.3(TERT):c.1026G>C (p.Arg342=)]
NM_198253.3(TERT):c.1026G>C (p.Arg342=)
Condition(s)
-
Homo sapiens translin-associated factor X, mRNA (cDNA clone MGC:13527 IMAGE:4283...
Homo sapiens translin-associated factor X, mRNA (cDNA clone MGC:13527 IMAGE:4283594), complete cdsgi|14714494|gb|BC010376.1|Nucleotide
-
PREDICTED: Homo sapiens ubiquitin A-52 residue ribosomal protein fusion product ...
PREDICTED: Homo sapiens ubiquitin A-52 residue ribosomal protein fusion product 1 (UBA52), transcript variant X5, mRNAgi|2462567272|ref|XM_054321937.1|Nucleotide
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Last Updated: Oct 26, 2024