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.

4 entries on 1 page. Showing entries 1 - 4.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

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Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

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Re-site     

VIP     

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Technique     

Tissue     

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Disease     

ID_report     

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Owner     
+/+ 12 c.2028C>A r.(?) p.(Cys676*) Laminin EGF-like 3 (641-693) Paternal (confirmed) - pathogenic g.216424384G>T g.216251042G>T - - USH2A_000334 Heterozygous PubMed: Baux 2014 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband F - France - - - - - 1 Anne-Françoise Roux
+/. 12 c.2028C>A r.(?) p.(Cys676*) - Parent #2 - pathogenic (recessive) g.216424384G>T g.216251042G>T - - USH2A_000334 - Tranebjaerg 2011, PubMed: Dad 2016 - - Germline - - - - - DNA SEQ - - retinal disease USH2-38 Tranebjaerg 2011, PubMed: Dad 2016 - F no Denmark - - - - - 1 LOVD
+?/. - c.2028C>A r.(?) p.(Cys676*) - Unknown ACMG likely pathogenic g.216424384G>T g.216251042G>T USH2A c.2028C>A, p.(Cys676*) - USH2A_000334 single heterozygous variant (recessive) PubMed: Jespersgaar 2019 - - Germline ? - - - - DNA SEQ-NG-I blood 125 genes associated with inherited retinal disorders, see paper supplemental data retinal disease 477 PubMed: Jespersgaar 2019 - ? - Denmark - - - - - 1 LOVD
+?/. - c.2028C>A r.(?) p.(Cys676*) - Unknown - likely pathogenic g.216424384G>T g.216251042G>T c.2028C>A, p.Cys676Ter - USH2A_000334 heterozygous PubMed: Zampaglione 2020 - - Unknown ? - - - - DNA SEQ-NG-I, PCRq blood - retinal disease OGI621_001276 PubMed: Zampaglione 2020 - ? - - - - - - - 1 LOVD
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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