NM_007123.5(USH2A):c.895del (p.Gln299fs) AND Usher syndrome

Clinical significance:Uncertain significance (Last evaluated: Jan 1, 2015)

Review status:(0/4) 0 stars out of maximum of 4 stars

no assertion criteria provided

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV000505121.2

Allele description [Variation Report for NM_007123.5(USH2A):c.895del (p.Gln299fs)]

NM_007123.5(USH2A):c.895del (p.Gln299fs)

Gene:
USH2A:usherin [Gene - OMIM - HGNC]
Variant type:
Deletion
Cytogenetic location:
1q41
Genomic location:
Preferred name:
NM_007123.5(USH2A):c.895del (p.Gln299fs)
HGVS:
  • NC_000001.11:g.216325555del
  • NG_009497.1:g.102844del
  • NM_007123.5:c.895del
  • NM_206933.3:c.895del
  • NP_009054.5:p.Gln299fs
  • NP_996816.2:p.Gln299fs
  • NC_000001.10:g.216498895del
  • NC_000001.10:g.216498897del
  • NM_206933.2:c.895delC
Protein change:
Q299fs
Links:
dbSNP: rs1338169194
NCBI 1000 Genomes Browser:
rs1338169194
Molecular consequence:
  • NM_007123.5:c.895del - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_206933.3:c.895del - frameshift variant - [Sequence Ontology: SO:0001589]

Condition(s)

Name:
Usher syndrome
Synonyms:
Usher Syndromes; Usher's syndrome
Identifiers:
MONDO: MONDO:0019501; MeSH: D052245; MedGen: C0271097; Orphanet: 886; OMIM: PS276900

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000598837NIHR Bioresource Rare Diseases, University of Cambridgeno assertion criteria providedUncertain significance
(Jan 1, 2015)
unknownresearch

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

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
South East Asianunknownyes1not providednot provided1not providedresearch

Citations

PubMed

Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease.

Carss KJ, Arno G, Erwood M, Stephens J, Sanchis-Juan A, Hull S, Megy K, Grozeva D, Dewhurst E, Malka S, Plagnol V, Penkett C, Stirrups K, Rizzo R, Wright G, Josifova D, Bitner-Glindzicz M, Scott RH, Clement E, Allen L, Armstrong R, Brady AF, et al.

Am J Hum Genet. 2017 Jan 5;100(1):75-90. doi: 10.1016/j.ajhg.2016.12.003. Epub 2016 Dec 29.

PubMed [citation]
PMID:
28041643
PMCID:
PMC5223092

Details of each submission

From NIHR Bioresource Rare Diseases, University of Cambridge, SCV000598837.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1South East Asian1not providednot providedresearch PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1unknownyes1not providednot provided1not providednot providednot provided

Last Updated: Oct 7, 2021

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