NM_133259.4(LRPPRC):c.3986-11_3986-8dup AND Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type

Clinical significance:Uncertain significance (Last evaluated: Jan 17, 2017)

Review status:1 star out of maximum of 4 stars

criteria provided, single submitter

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV000664704.1

Allele description [Variation Report for NM_133259.4(LRPPRC):c.3986-11_3986-8dup]

NM_133259.4(LRPPRC):c.3986-11_3986-8dup

Gene:
LRPPRC:leucine rich pentatricopeptide repeat containing [Gene - OMIM - HGNC]
Variant type:
Duplication
Cytogenetic location:
2p21
Genomic location:
Preferred name:
NM_133259.4(LRPPRC):c.3986-11_3986-8dup
HGVS:
  • NC_000002.12:g.43889887_43889890dup
  • NG_008247.1:g.111119_111122dup
  • NM_133259.4:c.3986-11_3986-8dupMANE SELECT
  • NC_000002.11:g.44117022_44117023insAAAG
  • NC_000002.11:g.44117026_44117029dup
  • NM_133259.3:c.3986-11_3986-8dupCTTT
  • NM_133259.3:c.3986-11_3986-8dupCTTT
Links:
dbSNP: rs764564351
NCBI 1000 Genomes Browser:
rs764564351
Molecular consequence:
  • NM_133259.4:c.3986-11_3986-8dup - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Name:
Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type (MC4DN5)
Synonyms:
Leigh syndrome, French Canadian type; Cox deficiency, French Canadian type; Cox deficiency, Saguenay Lac saint Jean type; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0009069; MedGen: C1857355; Orphanet: 70472; OMIM: 220111

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000788708Counsylcriteria provided, single submitter
Uncertain significance
(Jan 17, 2017)
unknownclinical testing

Citation Link

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedunknownunknownnot providednot providednot providednot providednot providedclinical testing

Details of each submission

From Counsyl, SCV000788708.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1unknownunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Oct 7, 2021

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