NC_012920.1(MT-ND5):m.13919T>C AND Leigh syndrome
- Germline classification:
- Uncertain significance (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:
- RCV000855011.1
Allele description [Variation Report for NC_012920.1(MT-ND5):m.13919T>C]
NC_012920.1(MT-ND5):m.13919T>C
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
-
MuF-like minor capsid protein [Microbacterium phage Balsa]
MuF-like minor capsid protein [Microbacterium phage Balsa]gi|1338671517|gb|AUX83530.1|Protein
-
Deinococcus sp. AJ005 plasmid p17k, complete sequence
Deinococcus sp. AJ005 plasmid p17k, complete sequencegi|1761809488|gb|CP044988.1|Nucleotide
-
Streptococcus sanguinis VMC66
Streptococcus sanguinis VMC66Reference genome for the Human Microbiome ProjectBioProject
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See more...Assertion and evidence details
Last Updated: May 19, 2024