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     

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AscendingDNA change (cDNA)     

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+/+ 17 c.3684T>A r.(?) p.(Cys1228*) Fibronectin type-III 2 (1145-1238) Parent #2 - pathogenic g.216373096A>T g.216199754A>T - - USH2A_000995 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband M - Italy - - - - - 1 Crystel Bonnet
+/. - c.3684T>A r.(?) p.(Cys1228 *) - Parent #2 - pathogenic (recessive) g.216373096A>T g.216199754A>T - - USH2A_000995 - PubMed: Karali 2019, Journal: Karali 2019 - - Germline - - - - - DNA SEQ-NG - - retinal disease Fam33P39 PubMed: Karali 2019, Journal: Karali 2019 - - - Italy - - - - - 1 Sandro Banfi
+?/. - c.3684T>A r.(?) p.(Cys1228*) - Parent #1 - likely pathogenic g.216373096A>T g.216199754A>T USH2A c.3684T>A, p.Cys1228X - USH2A_000995 compound heterozygous PubMed: Jauregui 2020 - - Unknown ? - - - - DNA SEQ-NG blood targeted sequencing retinal disease 134 PubMed: Jauregui 2020 - M - (United States) white - - - - 1 LOVD
+/. 17 c.3684T>A r.(?) p.(Cys1228*) - Both (homozygous) - pathogenic g.216373096A>T - c.3684T>A - USH2A_000995 - PubMed: Colombo-2020 - - Germline - - - - - DNA SEQ - - retinal disease - PubMed: Colombo-2020 - M no - - - - - - 1 LOVD
+/. - c.3684T>A r.(?) p.(Cys1228Ter) - Unknown ACMG pathogenic g.216373096A>T g.216199754A>T - - USH2A_000995 ACMG GN005 criteria: PVS1_VS PM2_P PM3_M PubMed: Bonnet, C. et al., 2016; PubMed: Colombo, L. et al., 2022; PubMed: Ganapathi, M. et al., 2022; PubMed: Karali, M. et al., 2019; PubMed: Colombo, L. et al., 2021; PubMed: Jauregui, R. et al., 2020 - rs2102466516 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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