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NC_012920.1:m.10106_15067del4962 AND Mitochondrial disease

Germline classification:
Pathogenic (1 submission)
Last evaluated:
May 22, 2017
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Somatic classification
of clinical impact:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Somatic classification
of oncogenicity:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Record status:
current
Accession:
RCV000495541.1

Allele description [Variation Report for NC_012920.1:m.10106_15067del4962]

NC_012920.1:m.10106_15067del4962

Genes:
  • MT-ND3:mitochondrially encoded NADH dehydrogenase 3 [Gene - OMIM - HGNC]
  • MT-ND4:mitochondrially encoded NADH dehydrogenase 4 [Gene - OMIM - HGNC]
  • MT-ND4L:mitochondrially encoded NADH dehydrogenase 4L [Gene - OMIM - HGNC]
  • MT-ND5:mitochondrially encoded NADH dehydrogenase 5 [Gene - OMIM - HGNC]
  • MT-ND6:mitochondrially encoded NADH dehydrogenase 6 [Gene - OMIM - HGNC]
  • MT-CYB:mitochondrially encoded cytochrome b [Gene - OMIM - HGNC]
  • MT-TR:mitochondrially encoded tRNA arginine [Gene - OMIM - HGNC]
  • MT-TE:mitochondrially encoded tRNA glutamic acid [Gene - OMIM - HGNC]
  • MT-TH:mitochondrially encoded tRNA histidine [Gene - OMIM - HGNC]
  • MT-TL2:mitochondrially encoded tRNA leucine 2 (CUN) [Gene - OMIM - HGNC]
  • MT-TS2:mitochondrially encoded tRNA serine 2 (AGU/C) [Gene - OMIM - HGNC]
Variant type:
Deletion
Genomic location:
Preferred name:
NC_012920.1:m.10106_15067del4962
HGVS:
  • NC_012920.1:m.10106_15067del
  • NC_012920.1:m.10106_15067del
  • NC_012920.1:m.10106_15067del
  • NC_012920.1:m.10106_15067del
  • NC_012920.1:m.10106_15067del
  • NC_012920.1:m.10106_15067del
  • NC_012920.1:m.10106_15067del
  • NC_012920.1:m.10106_15067del
  • NC_012920.1:m.10106_15067del
  • NC_012920.1:m.10106_15067del
  • NC_012920.1:m.10106_15067del
  • NC_012920.1:m.10106_15067del4962
Observations:
1

Condition(s)

Name:
Mitochondrial disease
Synonyms:
Mitochondrial diseases; Mitochondrial disorder
Identifiers:
MONDO: MONDO:0044970; MeSH: D028361; MedGen: C0751651; Orphanet: 68380

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000577885Wellcome Centre for Mitochondrial Research, Newcastle University
no assertion criteria provided
Pathogenic
(May 22, 2017) 		germlineclinical testing

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyes1not providednot providednot providednot providedclinical testing

Details of each submission

From Wellcome Centre for Mitochondrial Research, Newcastle University, SCV000577885.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot provided1not providednot providednot provided

Last Updated: Dec 9, 2023