NM_025137.4(SPG11):c.6953G>A (p.Arg2318His) AND not specified
- Germline classification:
- Benign (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001700698.1
Allele description [Variation Report for NM_025137.4(SPG11):c.6953G>A (p.Arg2318His)]
NM_025137.4(SPG11):c.6953G>A (p.Arg2318His)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Apr 9, 2023