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.

6 entries on 1 page. Showing entries 1 - 6.
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Effect     

Exon     

AscendingDNA change (cDNA)     

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DNA change (hg38)     

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Owner     
+/+ 48 c.9459C>A r.(?) p.(Cys3153*) Fibronectin type-III 18 (3110-3200) Unknown - pathogenic g.215990450G>T g.215817108G>T - - USH2A_000613 Heterozygous; Pathogenic PubMed: Le Quesne Stabej 2012 - - Germline - - +AluI;+CviKI_1;- HinP1I;-HhaI; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+?/. - c.9459C>A r.(?) p.(Cys3153*) - Unknown - likely pathogenic g.215990450G>T g.215817108G>T - - USH2A_000613 no variant 2nd chromosome PubMed: Stone 2017 - - Germline - - - - - DNA SEQ-NG - - retinal disease 592 PubMed: Stone 2017 1 affected F - (United States) - - - - - 1 LOVD
+?/. - c.9459C>A r.(?) p.(Cys3153*) - Unknown - likely pathogenic g.215990450G>T g.215817108G>T c.9459C>A p.(Cys3153*), c.1333513347delinsCTTG p.(Glu4445_4449delinsAspLeu) - USH2A_000613 - PubMed: Hagag 2020 - - Germline/De novo (untested) ? - - - - DNA ? - - retinal disease Subject 053 PubMed: Hagag 2020 - ? - - - - - - - 1 LOVD
+?/. - c.9459C>A r.(?) p.(Cys3153*) - Parent #2 - likely pathogenic g.215990450G>T g.215817108G>T USH2A c.9459C>A, p.C3153X - USH2A_000613 compound heterozygous PubMed: Jauregui 2020 - - Unknown ? - - - - DNA SEQ-NG blood targeted sequencing retinal disease 145 PubMed: Jauregui 2020 - M - (United States) white - - - - 1 LOVD
+/. 48 c.9459C>A r.(?) p.(Cys3153*) - Parent #2 - pathogenic g.215990450G>T - c.9459C>A - USH2A_000613 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - F - - - - - - - 1 Daan Panneman
+?/. - c.9459C>A r.(?) p.(Cys3153Ter) - Unknown ACMG likely pathogenic g.215990450G>T g.215817108G>T - - USH2A_000613 ACMG GN005 criteria: PVS1_VS PM2_P PubMed: Le Quesne Stabej, P. et al., 2012; PubMed: Jauregui, R. et al., 2020 - rs73090721 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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