NM_001283009.2(RTEL1):c.1301C>T (p.Thr434Met) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 25, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000795835.7
Allele description [Variation Report for NM_001283009.2(RTEL1):c.1301C>T (p.Thr434Met)]
NM_001283009.2(RTEL1):c.1301C>T (p.Thr434Met)
Condition(s)
Assertion and evidence details
Last Updated: Jun 9, 2024