NM_001283009.2(RTEL1):c.1761G>A (p.Pro587=) AND not specified
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Sep 23, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000501659.8
Allele description [Variation Report for NM_001283009.2(RTEL1):c.1761G>A (p.Pro587=)]
NM_001283009.2(RTEL1):c.1761G>A (p.Pro587=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024