NM_003172.4(SURF1):c.665C>G (p.Pro222Arg) AND Leigh syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 25, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002988543.2
Allele description [Variation Report for NM_003172.4(SURF1):c.665C>G (p.Pro222Arg)]
NM_003172.4(SURF1):c.665C>G (p.Pro222Arg)
Condition(s)
- Name:
- Leigh syndrome (NULS)
- Synonyms:
- Leigh Disease; Subacute necrotizing encephalopathy; Necrotizing encephalopathy infantile subacute of Leigh; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0009723; MedGen: C0023264; Orphanet: 506; OMIM: 256000
-
7eggc.vip5BJ (0)
BioProject
-
-eggc.vipWm1 (0)
BioProject
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See more...Assertion and evidence details
Last Updated: May 19, 2024