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.

5 entries on 1 page. Showing entries 1 - 5.
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Effect     

Exon     

AscendingDNA change (cDNA)     

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DNA change (hg38)     

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Owner     
+?/? 35 c.6795_6797del r.(?) p.(p.Glu2265_Tyr2266delinsAsp) Fibronectin type-III 9 (2241-2325) Unknown ACMG VUS g.216166371_216166373del g.215993029_215993031del 6795_6797delATA - USH2A_000483 Heterozygous; Pathogenic PubMed: Le Quesne Stabej 2012 - - Germline - - +AlwI;+Sau3AI;+MboI;+DpnI;+BfuCI;+DpnII; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/. 35 c.6795_6797del r.(?) p.(Glu2265_Tyr2266delinsAsp) - Parent #2 - pathogenic (recessive) g.216166371_216166373del g.215993029_215993031del 6795_6797delATA - USH2A_000483 possible duplicate PubMed: Dreyer 2000, PubMed: Dreyer 2008, PubMed: Dad 2016 - - Germline - - - - - DNA SEQ - - retinal disease USH2-24 (D53) PubMed: Dreyer 2000, PubMed: Dreyer 2008, PubMed: Dad 2016 - M no Denmark - - - - - 1 Anne-Françoise Roux
+/. - c.6795_6797del r.(?) p.(Glu2265_Tyr2266delinsAsp) - Parent #2 - pathogenic g.216166371_216166373del g.215993029_215993031del - - USH2A_000483 - PubMed: Ge 2015 - - Germline - - - - - DNA SEQ-NG - 195-gene panel retinal disease 32V+Y.3 PubMed: Ge 2015 simplex case - - United States - - - - - 1 LOVD
+?/. - c.6795_6797del r.(?) p.(Glu2265_Tyr2266delinsAsp) - Parent #2 - likely pathogenic g.216166371_216166373del g.215993029_215993031del USH2A c.6795_6797del - USH2A_000483 protein variant annotation not written; heterozygous PubMed: Toms 2020 - - Unknown ? - - - - ? ? - retrospective cohort retinal disease 42 PubMed: Toms 2020 - ? - United Kingdom (Great Britain) - - - - - 1 LOVD
?/. - c.6795_6797del r.(?) p.(Glu2265_Tyr2266delinsAsp) - Unknown ACMG VUS g.216166371_216166373del g.215993029_215993031del - - USH2A_000483 ACMG GN005 criteria: PM2_P PM3_P PubMed: Le Quesne Stabej, P. et al., 2012 - rs727503723 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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