NM_002693.2(POLG):c.2419C>T (p.Arg807Cys) AND Cerebellar ataxia infantile with progressive external ophthalmoplegia

Clinical significance:Pathogenic (Last evaluated: Dec 18, 2017)

Review status:1 star out of maximum of 4 stars

criteria provided, single submitter

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV000626194.1

Allele description [Variation Report for NM_002693.2(POLG):c.2419C>T (p.Arg807Cys)]

NM_002693.2(POLG):c.2419C>T (p.Arg807Cys)

Gene:
POLG:DNA polymerase gamma, catalytic subunit [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
15q26.1
Genomic location:
Preferred name:
NM_002693.2(POLG):c.2419C>T (p.Arg807Cys)
HGVS:
  • NC_000015.10:g.89322749G>A
  • NG_008218.2:g.17047C>T
  • NM_002693.2:c.2419C>T
  • NP_002684.1:p.Arg807Cys
  • LRG_765t1:c.2419C>T
  • LRG_765:g.17047C>T
  • LRG_765p1:p.Arg807Cys
  • NC_000015.9:g.89865980G>A
  • P54098:p.Arg807Cys
Protein change:
R807C
Links:
UniProtKB: P54098#VAR_058887; dbSNP: rs769827124
NCBI 1000 Genomes Browser:
rs769827124
Molecular consequence:
  • NM_002693.2:c.2419C>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Cerebellar ataxia infantile with progressive external ophthalmoplegia (PEOB1)
Synonyms:
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 1; PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE 1; Autosomal Recessive Progressive External Ophthalmoplegia
Identifiers:
MedGen: C4225153; Orphanet: 254886; OMIM: 258450

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000746834Genomic Research Center,Shahid Beheshti University of Medical Sciencescriteria provided, single submitter
Pathogenic
(Dec 18, 2017)
inheritedclinical testing

PubMed (1)
[See all records that cite this PMID]

Summary from all submissions

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

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]
PMID:
25741868
PMCID:
PMC4544753

Details of each submission

From Genomic Research Center,Shahid Beheshti University of Medical Sciences, SCV000746834.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1inheritedunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Apr 17, 2019

Support Center