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.

13 entries on 1 page. Showing entries 1 - 13.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

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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     

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Methylation     

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Disease     

ID_report     

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Owner     
+/+ 45 c.8981G>A r.(?) p.(Trp2994*) Fibronectin type-III 16 (2925-3015) Parent #2 - pathogenic g.216019240C>T g.215845898C>T - - USH2A_000232 Heterozygous PubMed: Yan 2009 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Yan 2009 Proband F - United States - - - - - 1 Anne-Françoise Roux
+/+ 45 c.8981G>A r.(?) p.(Trp2994*) Fibronectin type-III 16 (2925-3015) Unknown - pathogenic g.216019240C>T g.215845898C>T - - USH2A_000232 Heterozygous PubMed: Yan 2009 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Yan 2009 Proband F - United States - - - - - 1 Anne-Françoise Roux
+/. - c.8981G>A r.(?) p.(Trp2994*) - Unknown - pathogenic (recessive) g.216019240C>T - 1:216019240C>T ENST00000307340.3:c.8981G>A (Trp2994Ter) - USH2A_000232 - PubMed: Carss 2017 - - Germline - - - - - DNA SEQ-NG - WES retinal disease B240076 PubMed: Carss 2017 - F - United Kingdom (Great Britain) - - - - - 1 LOVD
+?/. - c.8981G>A r.(?) p.(Trp2994*) - Parent #1 - likely pathogenic g.216019240C>T g.215845898C>T - - USH2A_000232 - PubMed: Stone 2017 - - Germline - - - - - DNA SEQ-NG - - retinal disease 590 PubMed: Stone 2017 1 affected F - (United States) - - - - - 1 LOVD
+?/. - c.8981G>A r.(?) p.(Trp2994*) - Unknown - likely pathogenic g.216019240C>T g.215845898C>T - - USH2A_000232 - PubMed: Ellingford 2016 - - Germline - - - - - DNA SEQ - 105-gene panel retinal disease 12007911 PubMed: Ellingford 2016 patient - - - - - - - - 1 LOVD
+/. 45 c.8981G>A r.(8981g>a) p.(Trp2994*) - Parent #1 ACMG pathogenic g.216019240C>T g.215845898C>T - - USH2A_000232 - Journal: Reurink 2021 - - Germline no - - - - DNA SEQ-NG - gene panel retinal disease W19-0944 Journal: Reurink 2021 - - - - - - - - - 1 Janine Reurink
+/. 45 c.8981G>A r.(8981g>a) p.(Trp2994*) - Parent #1 ACMG pathogenic g.216019240C>T g.215845898C>T - - USH2A_000232 - Journal: Reurink 2021 - - Germline no - - - - DNA SEQ-NG - gene panel retinal disease W19-0948 Journal: Reurink 2021 - - - - - - - - - 1 Janine Reurink
+?/. - c.8981G>A r.(?) p.(Trp2994*) - Unknown - likely pathogenic g.216019240C>T g.215845898C>T c.13274C>T p.(Thr44251Met), c.8981G>A p.(Trp2994*) - USH2A_000232 - PubMed: Hagag 2020 - - Germline/De novo (untested) ? - - - - DNA ? - - retinal disease Subject 040 PubMed: Hagag 2020 - ? - - - - - - - 1 LOVD
+/. - c.8981G>A r.(?) p.(Trp2994*) - Unknown - pathogenic g.216019240C>T g.215845898C>T c.8981G>A, p.Trp2994Ter - USH2A_000232 heterozygous PubMed: Zampaglione 2020 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ blood - retinal disease OGI616_001265 PubMed: Zampaglione 2020 - ? - - - - - - - 1 LOVD
+?/. - c.8981G>A r.(?) p.(Trp2994*) - Parent #1 - likely pathogenic g.216019240C>T g.215845898C>T USH2A c.8981G>A - USH2A_000232 protein variant annotation not written; heterozygous PubMed: Toms 2020 - - Unknown ? - - - - ? ? - retrospective cohort retinal disease 18 PubMed: Toms 2020 - ? - United Kingdom (Great Britain) - - - - - 1 LOVD
+/. - c.8981G>A r.(?) p.(Trp2994*) - Parent #1 ACMG pathogenic g.216019240C>T g.215845898C>T USH2A c.8981G>A, p.(Trp2994*) - USH2A_000232 heterozygous PubMed: Reurink 2021 - - Unknown ? - - - - DNA SEQ-NG-I - molecular inversion probe-based sequencing retinal disease W19-0944 PubMed: Reurink 2021 genetically unexplained subjects from centers in the Netherlands, Ireland and Poland ? - Netherlands - - - - - 1 LOVD
+/. - c.8981G>A r.(?) p.(Trp2994*) - Parent #1 ACMG pathogenic g.216019240C>T g.215845898C>T USH2A c.8981G>A, p.(Trp2994*) - USH2A_000232 heterozygous PubMed: Reurink 2021 - - Unknown ? - - - - DNA SEQ-NG-I - molecular inversion probe-based sequencing retinal disease W19-0948 PubMed: Reurink 2021 genetically unexplained subjects from centers in the Netherlands, Ireland and Poland ? - Netherlands - - - - - 1 LOVD
+/. - c.8981G>A r.(?) p.(Trp2994Ter) - Unknown ACMG pathogenic g.216019240C>T g.215845898C>T - - USH2A_000232 ACMG GN005 criteria: PVS1_VS PM2_P PM3_P PubMed: Reurink, J. et al., 2021; PubMed: Yan, D. et al., 2009 - rs397518041 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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