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.

15 entries on 1 page. Showing entries 1 - 15.
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Effect     

Exon     

AscendingDNA change (cDNA)     

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+/+ 44 c.8740C>T r.(?) p.(Arg2914*) Fibronectin type-III 15 (2821-2920) Paternal (confirmed) - pathogenic g.216040454G>A g.215867112G>A - - USH2A_000275 Heterozygous PubMed: Baux 2014 - - Germline - - +DdeI;+BspCNI;+AluI; - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband M - Italy - - - - - 1 Anne-Françoise Roux
+/+ 44 c.8740C>T r.(?) p.(Arg2914*) Fibronectin type-III 15 (2821-2920) Paternal (confirmed) - pathogenic g.216040454G>A g.215867112G>A - - USH2A_000275 Heterozygous PubMed: Baux 2014 - - Germline - - +DdeI;+BspCNI;+AluI; - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband F - France - - - - - 1 Anne-Françoise Roux
+/+ 44 c.8740C>T r.(?) p.(Arg2914*) Fibronectin type-III 15 (2821-2920) Unknown - pathogenic g.216040454G>A g.215867112G>A - - USH2A_000275 Heterozygous PubMed: McGee 2010 - - Germline - - +DdeI;+BspCNI;+AluI; - - DNA SEQ - - USH2 - PubMed: McGee 2010 No genotype in the publication - - United States - - - - - 1 Anne-Françoise Roux
+/+ 44 c.8740C>T r.(?) p.(Arg2914*) Fibronectin type-III 15 (2821-2920) Paternal (confirmed) - pathogenic g.216040454G>A g.215867112G>A - - USH2A_000275 Heterozygous PubMed: Baux 2014 - - Germline - - +DdeI;+BspCNI;+AluI; - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband F - France - - - - - 1 Anne-Françoise Roux
+/+ 44 c.8740C>T r.(?) p.(Arg2914*) Fibronectin type-III 15 (2821-2920) Parent #2 - pathogenic g.216040454G>A g.215867112G>A - - USH2A_000275 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband - - Slovenia - - - - - 1 Crystel Bonnet
+?/. - c.8740C>T r.(?) p.(Arg2914*) - Unknown - likely pathogenic g.216040454G>A g.215867112G>A - - USH2A_000275 - PubMed: Ellingford 2016 - - Germline - - - - - DNA SEQ - 105-gene panel retinal disease 12013066 PubMed: Ellingford 2016 familial segregation analysis requested - - - - - - - - 1 LOVD
+/. - c.8740C>T r.(?) p.(Arg2914Ter) - Unknown - pathogenic g.216040454G>A g.215867112G>A - - USH2A_000275 - PubMed: Zhao 2015 - - Germline - - - - - DNA SEQ-NG - 86-gene panel retinal disease RD1200002 PubMed: Zhao 2015 simplex case - - Northern Ireland - - - - - 1 LOVD
+/. 44 c.8740C>T r.(8740c>u) p.(Arg2914*) - Parent #1 ACMG pathogenic g.216040454G>A g.215867112G>A - - USH2A_000275 - Journal: Reurink 2021 - - Germline no - - - - DNA SEQ-NG - gene panel retinal disease W19-0945 Journal: Reurink 2021 - - - - - - - - - 1 Janine Reurink
+/. 44 c.8740C>T r.(8740c>u) p.(Arg2914*) - Parent #2 ACMG pathogenic g.216040454G>A g.215867112G>A - - USH2A_000275 - Journal: Reurink 2021 - - Germline no - - - - DNA SEQ-NG - gene panel retinal disease W19-0948 Journal: Reurink 2021 - - - - - - - - - 1 Janine Reurink
+?/. - c.8740C>T r.(?) p.(Arg2914*) - Parent #1 - likely pathogenic g.216040454G>A g.215867112G>A USH2A, variant 1: c.8740C>T/p.R2914*, variant 2 :Deletion exon 5-32 - USH2A_000275 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET8 targeted sequencing panel - see paper retinal disease 1244 PubMed: Weisschuh 2020 Filing key number: 1014, sporadic retinitis pigmentosa, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
+/. - c.8740C>T r.(?) p.(Arg2914*) - Parent #1 ACMG pathogenic g.216040454G>A g.215867112G>A USH2A c.8740C>T, p.(Arg2914*) - USH2A_000275 heterozygous PubMed: Reurink 2021 - - Unknown ? - - - - DNA SEQ-NG-I - molecular inversion probe-based sequencing retinal disease W19-0945 PubMed: Reurink 2021 genetically unexplained subjects from centers in the Netherlands, Ireland and Poland ? - Netherlands - - - - - 1 LOVD
+/. - c.8740C>T r.(?) p.(Arg2914*) - Parent #2 ACMG pathogenic g.216040454G>A g.215867112G>A USH2A c.8740C>T, p.(Arg2914*) - USH2A_000275 heterozygous PubMed: Reurink 2021 - - Unknown ? - - - - DNA SEQ-NG-I - molecular inversion probe-based sequencing retinal disease W19-0948 PubMed: Reurink 2021 genetically unexplained subjects from centers in the Netherlands, Ireland and Poland ? - Netherlands - - - - - 1 LOVD
+/. 44 c.8740C>T r.(8740c>u) p.(Arg2914Ter) - Parent #1 ACMG pathogenic g.216040454G>A g.215867112G>A - - USH2A_000275 - PubMed: Reurink 2023, Journal: Reurink 2023 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease USH19 PubMed: Reurink 2023, Journal: Reurink 2023 - - - - - - - - - 1 Janine Reurink
+/. - c.8740C>T r.(?) p.(Arg2914Ter) - Unknown ACMG pathogenic g.216040454G>A g.215867112G>A - - USH2A_000275 ACMG GN005 criteria: PVS1_VS PM2_P PM3_M PubMed: Reurink, J. et al., 2021; PubMed: Bonnet, C. et al., 2016; PubMed: Weisschuh, N. et al., 2020 - rs766590491 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.8740C>T r.(?) p.(Arg2914Ter) - Paternal (confirmed) ACMG pathogenic (recessive) g.216040454G>A g.215867112G>A - - USH2A_000275 ACMG PM2, PVS1, PP5 PubMed: Weisschuh 2024 228417 - Germline - - - - - DNA SEQ-NG - WGS ? USHII-320 PubMed: Weisschuh 2024 patient, no family history F - Germany - - - - - 1 Johan den Dunnen
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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