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.

10 entries on 1 page. Showing entries 1 - 10.
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+?/? 11 c.1859G>T r.(?) p.(Cys620Phe) Laminin EGF-like 2 (575-640) Paternal (confirmed) ACMG VUS g.216462734C>A g.216289392C>A - - USH2A_000572 Heterozygous; Pathogenic PubMed: Le Quesne Stabej 2012, USMA missense analysis, missense variant in MSV3d - - Germline - 0/878 controls -HpyCH4V - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+?/? 11 c.1859G>T r.(?) p.(Cys620Phe) Laminin EGF-like 2 (575-640) Unknown ACMG VUS g.216462734C>A g.216289392C>A - - USH2A_000572 Heterozygous; Pathogenic PubMed: Le Quesne Stabej 2012, USMA missense analysis, missense variant in MSV3d - - Germline - 0/878 controls -HpyCH4V - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+?/? 11 c.1859G>T r.(?) p.(Cys620Phe) Laminin EGF-like 2 (575-640) Unknown ACMG VUS g.216462734C>A g.216289392C>A - - USH2A_000572 Heterozygous; Pathogenic PubMed: Le Quesne Stabej 2012, USMA missense analysis, missense variant in MSV3d - - Germline - 0/878 controls -HpyCH4V - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+?/. - c.1859G>T r.(?) p.(Cys620Phe) - Unknown - likely pathogenic g.216462734C>A g.216289392C>A - - USH2A_000572 - PubMed: Ellingford 2016 - - Germline - - - - - DNA SEQ - 105-gene panel retinal disease 12000462 PubMed: Ellingford 2016 patient - - - - - - - - 1 LOVD
+?/. - c.1859G>T r.(?) p.(Cys620Phe) - Unknown - likely pathogenic g.216462734C>A g.216289392C>A c.1859G>T p.(Cys620Phe), c.4821G>A p.(Trp1607*) - USH2A_000572 - PubMed: Hagag 2020 - - Germline/De novo (untested) ? - - - - DNA ? - - retinal disease Subject 024 PubMed: Hagag 2020 - ? - - - - - - - 1 LOVD
+?/. - c.1859G>T r.(?) p.(Cys620Phe) - Unknown - likely pathogenic g.216462734C>A g.216289392C>A USH2A;NM_206933.2;c.[1859G>T];[14803C>T];p.[(Cys620Phe)];[(Arg4935*)] - USH2A_000572 compound heterozygous PubMed: Jiman 2020 - - Unknown ? - - - - DNA SEQ-NG-I - 176 genes panel retinal disease 13 PubMed: Jiman 2020 - M - (United Kingdom (Great Britain)) - - - - - 1 LOVD
+?/. 11 c.1859G>T r.(?) p.(Cys620Phe) - Unknown - likely pathogenic g.216462734C>A - c.1859G>T,p.C620F - USH2A_000572 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
+?/. - c.1859G>T r.(?) p.(Cys620Phe) - Parent #1 - likely pathogenic g.216462734C>A g.216289392C>A USH2A c.1859G>T, p.(Cys620Phe) - USH2A_000572 heterozygous PubMed: Molina-Ramirez 2020 - - Unknown ? - - - - DNA SEQ-NG-I - 14 patients: 105-gene panel, 13 samples: 176-gene panel using previously described method (O', Sullivan J et al. 2012) USH 12000462 PubMed: Molina-Ramirez 2020 - M - United Kingdom (Great Britain) - - - - - 1 LOVD
+?/. - c.1859G>T r.(?) p.(Cys620Phe) - Parent #2 - likely pathogenic g.216462734C>A g.216289392C>A USH2A c.1859G>T - USH2A_000572 protein variant annotation not written; heterozygous PubMed: Toms 2020 - - Unknown ? - - - - ? ? - retrospective cohort retinal disease 2 PubMed: Toms 2020 - ? - United Kingdom (Great Britain) - - - - - 1 LOVD
+?/. - c.1859G>T r.(?) p.(Cys620Phe) - Unknown ACMG likely pathogenic g.216462734C>A g.216289392C>A - - USH2A_000572 ACMG GN005 criteria: PM2_P PM3_P PP3_P PubMed: Molina-Ramirez, L. P. et al., 2020; PubMed: Le Quesne Stabej, P. et al., 2012; PubMed: Toms, M. et al., 2020 - rs758571672 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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