Full data view for gene USH2A


This database is one of the ”Retinal and hearing impairment genetic variant databases”.
Information The variants shown are described using the NM_206933.2 transcript reference sequence.

3 entries on 1 page. Showing entries 1 - 3.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

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VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/+ 62 c.12172_12174delinsTAAA r.(?) p.(Leu4058*) Fibronectin type-III 25 (3961-4062) Paternal (inferred) - pathogenic g.215853611_215853613delinsTTTA g.215680269_215680271delinsTTTA - - USH2A_000750 Homozygous PubMed: Baux 2014 - - Germline - - - Hpy188I;-MlyI;-PleI; - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband M - France - - - - - 1 Anne-Françoise Roux
+/+ 62 c.12172_12174delinsTAAA r.(?) p.(Leu4058*) Fibronectin type-III 25 (3961-4062) Maternal (inferred) - pathogenic g.215853611_215853613delinsTTTA g.215680269_215680271delinsTTTA - - USH2A_000750 Homozygous PubMed: Baux 2014 - - Germline - - - Hpy188I;-MlyI;-PleI; - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband M - France - - - - - 1 Anne-Françoise Roux
+?/. - c.12172_12174delinsTAAA r.(?) p.(Leu4058*) - Unknown - likely pathogenic g.215853611_215853613delinsTTTA g.215680269_215680271delinsTTTA USH2A c.12172_12172delCTGinsTAAA, p.Leu4058fs - USH2A_000750 error in annotation, protein change is immediate stop and not frameshift, only novel variants described in detail in the paper; original cohort contained over 750 patients from over 520 pedigrees, PubMed: Dockery 2017 - - Germline yes - - - - DNA SEQ-NG-I blood panel of 254 genes implicated in retinopathies retinal disease 4 PubMed: Dockery 2017 no patient numbers in the paper, consecutive numbers given ? - Ireland - - - - - 1 LOVD
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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