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.

13 entries on 1 page. Showing entries 1 - 13.
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+/+ 44 c.8834G>A r.(?) p.(Trp2945*) Fibronectin type-III 16 (2925-3015) Paternal (confirmed) - pathogenic g.216040360C>T g.215867018C>T - - USH2A_000584 Heterozygous; Pathogenic PubMed: Le Quesne Stabej 2012 - - Germline - 0/878 controls none - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/+ 44 c.8834G>A r.(?) p.(Trp2945*) Fibronectin type-III 16 (2925-3015) Maternal (confirmed) - pathogenic g.216040360C>T g.215867018C>T - - USH2A_000584 Heterozygous; likely pathogenic PubMed: Glöckle 2014 - - Germline - - none - - DNA SEQ, SEQ-NG-S - - RPar - PubMed: Glöckle 2014 Proband - - - - - - - - 1 Anne-Françoise Roux
+/+ 44 c.8834G>A r.(?) p.(Trp2945*) Fibronectin type-III 16 (2925-3015) Parent #1 - pathogenic g.216040360C>T g.215867018C>T - - USH2A_000584 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband F - Germany - - - - - 1 Crystel Bonnet
+/+ 44 c.8834G>A r.(?) p.(Trp2945*) Fibronectin type-III 16 (2925-3015) Parent #1 - pathogenic g.216040360C>T g.215867018C>T - - USH2A_000584 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband F - Germany - - - - - 1 Crystel Bonnet
+/. - c.8834G>A r.(?) p.(Trp2945Ter) - Unknown - pathogenic g.216040360C>T g.215867018C>T - - USH2A_000584 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.8834G>A r.(?) p.(Trp2945*) - Parent #1 - pathogenic g.216040360C>T g.215867018C>T - - USH2A_000584 - PubMed: Neuhaus 2017 - - Germline - - - - - DNA SEQ - - USH Pat126 PubMed: Neuhaus 2017 - - no Germany - - - - - 1 LOVD
+?/. - c.8834G>A r.(?) p.(Trp2945*) - Unknown - likely pathogenic g.216040360C>T g.215867018C>T c.2299delG p.(Glu767Serfs*21), c.8834G>A p.(Trp2945*) - USH2A_000584 - PubMed: Hagag 2020 - - Germline/De novo (untested) ? - - - - DNA ? - - retinal disease Subject 023 PubMed: Hagag 2020 - ? - - - - - - - 1 LOVD
+/. - c.8834G>A r.(?) p.(Trp2945*) - Unknown - pathogenic g.216040360C>T g.215867018C>T c.8834G>A, p.Trp2945Ter - USH2A_000584 heterozygous PubMed: Zampaglione 2020 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ blood - retinal disease 184-059 PubMed: Zampaglione 2020 - ? - - - - - - - 1 LOVD
+?/. - c.8834G>A r.(?) p.(Trp2945*) - Parent #1 - likely pathogenic g.216040360C>T g.215867018C>T USH2A, variant 1: c.8834G>A/p.W2945*, variant 2 :Deletion exon 22-24 - USH2A_000584 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET7 targeted sequencing panel - see paper retinal disease 43 PubMed: Weisschuh 2020 Filing key number: 23, Usher syndrome type 2, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
+?/. - c.8834G>A r.(?) p.(Trp2945*) - Parent #1 - likely pathogenic g.216040360C>T g.215867018C>T USH2A, variant 1: c.6383G>A/p.C2128Y, variant 2: c.8834G>A/p.W2945* - USH2A_000584 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET3 targeted sequencing panel - see paper retinal disease 550 PubMed: Weisschuh 2020 Filing key number: 195, Usher syndrome type 2, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
+?/. - c.8834G>A r.(?) p.(Trp2945*) - Parent #1 - likely pathogenic g.216040360C>T g.215867018C>T USH2A, variant 1: c.2276G>T/p.C759F, variant 2: c.8834G>A/p.W2945* - USH2A_000584 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET1 targeted sequencing panel - see paper retinal disease 1067 PubMed: Weisschuh 2020 Filing key number: 677, sporadic retinitis pigmentosa, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
+/. 44 c.8834G>A r.(?) p.(Trp2945*) - Unknown - pathogenic (recessive) g.216040360C>T - c.8834G>A - USH2A_000584 - PubMed: Colombo-2020 - rs760302201 Germline yes - - - - DNA SEQ - - retinal disease - PubMed: Colombo-2020 - F no - - - - - - 1 LOVD
+/. - c.8834G>A r.(?) p.(Trp2945Ter) - Unknown ACMG pathogenic g.216040360C>T g.215867018C>T - - USH2A_000584 ACMG GN005 criteria: PVS1_VS PM2_P PM3_S PubMed: Bonnet, C. et al., 2016; PubMed: Le Quesne Stabej, P. et al., 2012; PubMed: Glockle, N. et al., 2014; PubMed: Colombo, L. et al., 2022; PubMed: Hu, J. et al., 2020; PubMed: Colombo, L. et al., 2021; PubMed: Neuhaus, C. et al., 2017 - rs760302201 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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