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NM_016247.4(IMPG2):c.1826del (p.Val609fs) AND Retinitis pigmentosa 56

Germline classification:
Pathogenic (1 submission)
Last evaluated:
Sep 18, 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:
RCV000625597.2

Allele description [Variation Report for NM_016247.4(IMPG2):c.1826del (p.Val609fs)]

NM_016247.4(IMPG2):c.1826del (p.Val609fs)

Gene:
IMPG2:interphotoreceptor matrix proteoglycan 2 [Gene - OMIM - HGNC]
Variant type:
Deletion
Cytogenetic location:
3q12.3
Genomic location:
Preferred name:
NM_016247.4(IMPG2):c.1826del (p.Val609fs)
HGVS:
  • NC_000003.12:g.101244505del
  • NG_028284.1:g.81071del
  • NM_016247.4:c.1826delMANE SELECT
  • NP_057331.2:p.Val609fs
  • NC_000003.11:g.100963349del
  • NM_016247.3:c.1826delT
Protein change:
V609fs
Links:
dbSNP: rs1553681433
NCBI 1000 Genomes Browser:
rs1553681433
Molecular consequence:
  • NM_016247.4:c.1826del - frameshift variant - [Sequence Ontology: SO:0001589]

Condition(s)

Name:
Retinitis pigmentosa 56 (RP56)
Identifiers:
MONDO: MONDO:0013314; MedGen: C3150819; Orphanet: 791; OMIM: 613581

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000746096Bioscientia Institut fuer Medizinische Diagnostik GmbH, Sonic Healthcare
no assertion criteria provided
Pathogenic
(Sep 18, 2017) 		germlineclinical testing

Help

Summary from all submissions

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

Details of each submission

From Bioscientia Institut fuer Medizinische Diagnostik GmbH, Sonic Healthcare, SCV000746096.1

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

Last Updated: Mar 4, 2023