NM_206933.4(USH2A):c.7027del (p.Arg2343fs) AND not provided

Clinical significance:Pathogenic (Last evaluated: May 1, 2019)

Review status:1 star out of maximum of 4 stars

criteria provided, single submitter

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV001091131.2

Allele description [Variation Report for NM_206933.4(USH2A):c.7027del (p.Arg2343fs)]

NM_206933.4(USH2A):c.7027del (p.Arg2343fs)

Gene:
USH2A:usherin [Gene - OMIM - HGNC]
Variant type:
Deletion
Cytogenetic location:
1q41
Genomic location:
Preferred name:
NM_206933.4(USH2A):c.7027del (p.Arg2343fs)
HGVS:
  • NC_000001.11:g.215965412del
  • NG_009497.1:g.462987del
  • NG_009497.2:g.463039del
  • NM_206933.4:c.7027delMANE SELECT
  • NP_996816.3:p.Arg2343fs
  • NC_000001.10:g.216138754del
  • NM_206933.2:c.7027del
Protein change:
R2343fs
Links:
dbSNP: rs1667316878
NCBI 1000 Genomes Browser:
rs1667316878
Molecular consequence:
  • NM_206933.4:c.7027del - frameshift variant - [Sequence Ontology: SO:0001589]
Observations:
3

Condition(s)

Identifiers:
MedGen: CN517202

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV001246999CeGaT Praxis fuer Humangenetik Tuebingencriteria provided, single submitter
Pathogenic
(May 1, 2019)
germlineclinical testing

Citation Link

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyes3not providednot providednot providednot providedclinical testing

Details of each submission

From CeGaT Praxis fuer Humangenetik Tuebingen, SCV001246999.6

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided3not providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot provided3not providednot providednot provided

Last Updated: Nov 27, 2021

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