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NM_001008212.2(OPTN):c.1204_1210del (p.Asn401_Asn402insTer) AND OPTN-related disorder

Germline classification:
Likely pathogenic (1 submission)
Last evaluated:
Jan 30, 2023
Review status:
1 star out of maximum of 4 stars
criteria provided, single submitter
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:
RCV004536679.1

Allele description [Variation Report for NM_001008212.2(OPTN):c.1204_1210del (p.Asn401_Asn402insTer)]

NM_001008212.2(OPTN):c.1204_1210del (p.Asn401_Asn402insTer)

Gene:
OPTN:optineurin [Gene - OMIM - HGNC]
Variant type:
Deletion
Cytogenetic location:
10p13
Genomic location:
Preferred name:
NM_001008212.2(OPTN):c.1204_1210del (p.Asn401_Asn402insTer)
HGVS:
  • NC_000010.11:g.13126001_13126007del
  • NG_012876.1:g.30920_30926del
  • NM_001008211.1:c.1204_1210del
  • NM_001008212.2:c.1204_1210delMANE SELECT
  • NM_001008213.1:c.1204_1210del
  • NM_021980.4:c.1204_1210del
  • NP_001008212.1:p.Asn401_Asn402insTer
  • NP_001008213.1:p.Asn401_Asn402insTer
  • NP_001008214.1:p.Asn401_Asn402insTer
  • NP_068815.2:p.Asn401_Asn402insTer
  • NC_000010.10:g.13168001_13168007del
  • NM_001008211.1:c.1204_1210del7
Molecular consequence:
  • NM_001008211.1:c.1204_1210del - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001008212.2:c.1204_1210del - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001008213.1:c.1204_1210del - nonsense - [Sequence Ontology: SO:0001587]
  • NM_021980.4:c.1204_1210del - nonsense - [Sequence Ontology: SO:0001587]

Condition(s)

Name:
OPTN-related disorder
Synonyms:
OPTN-Related Disorders; OPTN-related condition
Identifiers:

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV004113818PreventionGenetics, part of Exact Sciences
criteria provided, single submitter

(ACMG Guidelines, 2015)		Likely pathogenic
(Jan 30, 2023) 		germlineclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot 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 PreventionGenetics, part of Exact Sciences, SCV004113818.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)

Description

The OPTN c.1204_1210del7 variant is predicted to result in premature protein termination (p.Asn402*). To our knowledge, this variant has not been reported in the literature. This variant is reported in 0.00088% of alleles in individuals of European (Non-Finnish) descent in gnomAD (http://gnomad.broadinstitute.org/variant/10-13167998-AATAATGC-A). Nonsense variants in OPTN are expected to be pathogenic. This variant is interpreted as likely pathogenic.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Jul 15, 2024