NM_206933.4(USH2A):c.13335_13347delinsCTTG (p.Glu4445_Ser4449delinsAspLeu) AND Retinal dystrophy

Clinical significance:Pathogenic (Last evaluated: May 17, 2019)

Review status:1 star out of maximum of 4 stars

criteria provided, single submitter

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV001074750.1

Allele description [Variation Report for NM_206933.4(USH2A):c.13335_13347delinsCTTG (p.Glu4445_Ser4449delinsAspLeu)]

NM_206933.4(USH2A):c.13335_13347delinsCTTG (p.Glu4445_Ser4449delinsAspLeu)

Gene:
USH2A:usherin [Gene - OMIM - HGNC]
Variant type:
Indel
Cytogenetic location:
1q41
Genomic location:
Preferred name:
NM_206933.4(USH2A):c.13335_13347delinsCTTG (p.Glu4445_Ser4449delinsAspLeu)
HGVS:
  • NC_000001.11:g.215674564_215674576delinsCAAG
  • NG_009497.1:g.753821_753833delinsCTTG
  • NG_009497.2:g.753873_753885delinsCTTG
  • NM_206933.4:c.13335_13347delinsCTTGMANE SELECT
  • NP_996816.3:p.Glu4445_Ser4449delinsAspLeu
  • NC_000001.10:g.215847906_215847918delinsCAAG
  • NM_206933.2:c.13335_13347delGAACATGGACTCTinsCTTG
Links:
dbSNP: rs1553252388
NCBI 1000 Genomes Browser:
rs1553252388
Molecular consequence:
  • NM_206933.4:c.13335_13347delinsCTTG - inframe_indel - [Sequence Ontology: SO:0001820]

Condition(s)

Name:
Retinal dystrophy
Identifiers:
MONDO: MONDO:0019118; MeSH: D058499; MedGen: C0854723; Human Phenotype Ontology: HP:0000556

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV001240345Blueprint Geneticscriteria provided, single submitter
Pathogenic
(May 17, 2019)
germlineclinical testing

Citation Link

Description

My Retina Tracker patient

SCV001240345

Summary from all submissions

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

Details of each submission

From Blueprint Genetics, SCV001240345.1

#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: Nov 27, 2021

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