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NM_002693.3(POLG):c.3511A>C (p.Asn1171His) AND not provided

Germline classification:
Uncertain significance (2 submissions)
Last evaluated:
Jun 14, 2018
Review status:
2 stars out of maximum of 4 stars
criteria provided, multiple submitters, no conflicts
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:
RCV000712804.6

Allele description [Variation Report for NM_002693.3(POLG):c.3511A>C (p.Asn1171His)]

NM_002693.3(POLG):c.3511A>C (p.Asn1171His)

Gene:
POLG:DNA polymerase gamma, catalytic subunit [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
15q26.1
Genomic location:
Preferred name:
NM_002693.3(POLG):c.3511A>C (p.Asn1171His)
HGVS:
  • NC_000015.10:g.89317508T>G
  • NG_008218.2:g.22288A>C
  • NG_011736.1:g.78546T>G
  • NM_001126131.2:c.3511A>C
  • NM_002693.3:c.3511A>CMANE SELECT
  • NP_001119603.1:p.Asn1171His
  • NP_002684.1:p.Asn1171His
  • NP_002684.1:p.Asn1171His
  • LRG_765t1:c.3511A>C
  • LRG_500:g.78546T>G
  • LRG_765:g.22288A>C
  • LRG_765p1:p.Asn1171His
  • NC_000015.9:g.89860739T>G
  • NM_002693.2:c.3511A>C
Protein change:
N1171H
Links:
dbSNP: rs1567184138
NCBI 1000 Genomes Browser:
rs1567184138
Molecular consequence:
  • NM_001126131.2:c.3511A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_002693.3:c.3511A>C - missense variant - [Sequence Ontology: SO:0001583]
Observations:
1

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000843337Athena Diagnostics
criteria provided, single submitter

(Athena Diagnostics Criteria)		Uncertain significance
(Jun 14, 2018) 		germlineclinical testing

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

SCV000859420Eurofins Ntd Llc (ga)
criteria provided, single submitter

(EGL Classification Definitions 2015)		Uncertain significance
(Jan 29, 2018) 		germlineclinical testing

Citation Link

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknown1not providednot providednot providednot providedclinical testing

Citations

PubMed

A Standardized DNA Variant Scoring System for Pathogenicity Assessments in Mendelian Disorders.

Karbassi I, Maston GA, Love A, DiVincenzo C, Braastad CD, Elzinga CD, Bright AR, Previte D, Zhang K, Rowland CM, McCarthy M, Lapierre JL, Dubois F, Medeiros KA, Batish SD, Jones J, Liaquat K, Hoffman CA, Jaremko M, Wang Z, Sun W, Buller-Burckle A, et al.

Hum Mutat. 2016 Jan;37(1):127-34. doi: 10.1002/humu.22918. Epub 2015 Oct 29.

PubMed [citation]
PMID:
26467025
PMCID:
PMC4737317

Details of each submission

From Athena Diagnostics, SCV000843337.1

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

From Eurofins Ntd Llc (ga), SCV000859420.1

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

Last Updated: Sep 29, 2024