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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Effect     

Exon     

AscendingDNA change (cDNA)     

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+/+ 59i c.11549-1G>A r.spl p.? - Unknown - pathogenic g.215914880C>T g.215741538C>T - - USH2A_000899 Heterozygous PubMed: Lenassi 2015 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Lenassi 2015 Proband - - Canada - - - - - 1 Eva Lenassi
+/+ 59i c.11549-1G>A r.spl p.? - Parent #2 - pathogenic g.215914880C>T g.215741538C>T - - USH2A_000899 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband F - Germany - - - - - 1 Crystel Bonnet
+/+ 59i c.11549-1G>A r.spl p.? - Parent #1 - pathogenic g.215914880C>T g.215741538C>T - - USH2A_000899 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S, PCRq, arrayCGH - - USH2 - PubMed: Bonnet 2016 Proband F - Germany - - - - - 1 Crystel Bonnet
?/. - c.11549-1G>A r.spl p.? - Unknown - VUS g.215914880C>T g.215741538C>T - - USH2A_000899 - PubMed: Ellingford 2016 - - Germline - - - - - DNA SEQ - 105-gene panel retinal disease 12011781 PubMed: Ellingford 2016 patient - - - - - - - - 1 LOVD
+/. - c.11549-1G>A r.spl p.? - Parent #2 - pathogenic g.215914880C>T g.215741538C>T - - USH2A_000899 - PubMed: Neuhaus 2017 - - Germline - - - - - DNA SEQ-NG - gene panel USH Pat66 PubMed: Neuhaus 2017 - - no Germany - - - - - 1 LOVD
+/. - c.11549-1G>A r.spl p.? - Parent #2 - pathogenic g.215914880C>T g.215741538C>T - - USH2A_000899 - PubMed: Neuhaus 2017 - - Germline - - - - - DNA SEQ - - USH Pat19 PubMed: Neuhaus 2017 - - no Germany - - - - - 1 LOVD
+?/. - c.11549-1G>A r.spl p.(?) - Parent #1 - likely pathogenic g.215914880C>T g.215741538C>T USH2A, variant 1: c.11549-1G>A/p.?, variant 2: c.14761G>T/p.E4921* - USH2A_000899 solved, compound heterozygous PubMed: Weisschuh 2020 - - Germline yes - - - - DNA SEQ-NG blood RET7 targeted sequencing panel - see paper retinal disease 692 PubMed: Weisschuh 2020 Filing key number: 251, Usher syndrome type 2, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
+?/. - c.11549-1G>A r.spl p.(?) - Parent #2 - likely pathogenic g.215914880C>T g.215741538C>T USH2A c.11549-1G>A - USH2A_000899 protein variant annotation not written; heterozygous PubMed: Toms 2020 - - Unknown ? - - - - ? ? - retrospective cohort retinal disease 36 PubMed: Toms 2020 - ? - United Kingdom (Great Britain) - - - - - 1 LOVD
+/. 59i c.11549-1G>A r.spl p.? - Parent #1 ACMG pathogenic g.215914880C>T g.215741538C>T - - USH2A_000899 - PubMed: de Bruijn 2023, PubMed: Reurink 2023, Journal: Reurink 2023 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease 073255;USH31 PubMed: de Bruijn 2023, PubMed: Reurink 2023, Journal: Reurink 2023 - - - - - - - - - 1 Janine Reurink
+/. - c.11549-1G>A r.spl p.? - Unknown ACMG pathogenic g.215914880C>T g.215741538C>T - - USH2A_000899 ACMG GN005 criteria: PVS1_VS PM2_P PM3_S PubMed: Lenassi, E. et al., 2015; PubMed: Bonnet, C. et al., 2016; PubMed: Weisschuh, N. et al., 2020; PubMed: Neuhaus, C. et al., 2017 - rs878853407 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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