NM_025137.4(SPG11):c.5608T>C (p.Leu1870=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 11, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002350282.2
Allele description [Variation Report for NM_025137.4(SPG11):c.5608T>C (p.Leu1870=)]
NM_025137.4(SPG11):c.5608T>C (p.Leu1870=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
MKRN2 makorin ring finger protein 2 [Canis lupus familiaris]
MKRN2 makorin ring finger protein 2 [Canis lupus familiaris]Gene ID:476531Gene
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024