NC_012920.1(MT-ATP6):m.9067A>G AND Leigh syndrome
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Oct 17, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000854418.1
Allele description [Variation Report for NC_012920.1(MT-ATP6):m.9067A>G]
NC_012920.1(MT-ATP6):m.9067A>G
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
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RefSeq RNA Links for Gene (Select 9519) (2)
Nucleotide
-
Related DataSets for GEO Profiles (Select 34499427) (1)
GEO DataSets
-
c-MYC depletion effect on carcinoma cell lines
c-MYC depletion effect on carcinoma cell linesAccession: GDS2526GEO DataSets
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dbVar for Gene (Select 6943) (140)
dbVar
-
PMC Links for Gene (Select 9519) (33)
PMC
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Last Updated: May 19, 2024