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.

16 entries on 1 page. Showing entries 1 - 16.
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Effect     

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AscendingDNA change (cDNA)     

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?/. - c.9433C>T r.(?) p.(Leu3145Phe) - Unknown - VUS g.215990476G>A g.215817134G>A USH2A(NM_206933.4):c.9433C>T (p.L3145F) - USH2A_001187 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.9433C>T r.(?) p.(Leu3145Phe) - Unknown - VUS g.215990476G>A g.215817134G>A USH2A(NM_206933.4):c.9433C>T (p.L3145F) - USH2A_001187 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.9433C>T r.(?) p.(Leu3145Phe) - Both (homozygous) - likely pathogenic g.215990476G>A g.215817134G>A - - USH2A_001187 - PubMed: Perez-Carro 2016 - - Germline yes - - - - DNA SEQ-NG - gene panel retinal disease RP-0338 PubMed: Perez-Carro 2016 - - - Spain - - - - - 1 LOVD
+?/. - c.9433C>T r.(?) p.(Leu3145Phe) - Parent #1 - likely pathogenic (recessive) g.215990476G>A g.215817134G>A - - USH2A_001187 - PubMed: Weisschuh 2016 - - Germline - - - - - DNA SEQ-NG - WES retinal disease ARRP82 PubMed: Weisschuh 2016 family - - Germany - - - - - 1 LOVD
+/. - c.9433C>T r.(?) p.(Leu3145Phe) - Parent #2 - pathogenic g.215990476G>A g.215817134G>A - - USH2A_001187 - PubMed: Ge 2015 - - Germline - - - - - DNA SEQ-NG - 195-gene panel retinal disease 5CV+J.77 PubMed: Ge 2015 simplex case - - United States - - - - - 1 LOVD
?/. 48 c.9433C>T r.(9433c>u) p.(Leu3145Phe) - Parent #2 ACMG VUS g.215990476G>A g.215817134G>A - - USH2A_001187 - Journal: Reurink 2021 - - Germline no - - - - DNA SEQ-NG - gene panel retinal disease W19-0120 Journal: Reurink 2021 - - - - - - - - - 1 Janine Reurink
+?/. - c.9433C>T r.(?) p.(Leu3145Phe) - Parent #1 - likely pathogenic g.215990476G>A g.215817134G>A USH2A, variant 1: c.9433C>T/p.L3145F, variant 2: c.13335_13347delinsCTTG/ p.E4445_S4449delinsDL - USH2A_001187 solved, compound heterozygous PubMed: Weisschuh 2020 - - Germline yes - - - - DNA SEQ blood Sanger sequencing retinal disease 239 PubMed: Weisschuh 2020 Filing key number: 82, autosomal recessive retinitis pigmentosa, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
+?/. - c.9433C>T r.(?) p.(Leu3145Phe) - Parent #1 - likely pathogenic g.215990476G>A g.215817134G>A USH2A, variant 1: c.9433C>T/p.L3145F, variant 2: c.13335_13347delinsCTTG/ p.E4445_S4449delinsDL - USH2A_001187 solved, compound heterozygous PubMed: Weisschuh 2020 - - Germline yes - - - - DNA SEQ-NG blood RET2 targeted sequencing panel - see paper retinal disease 240 PubMed: Weisschuh 2020 Filing key number: 82, autosomal recessive retinitis pigmentosa, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
+?/. - c.9433C>T r.(?) p.(Leu3145Phe) - Parent #1 - likely pathogenic g.215990476G>A g.215817134G>A USH2A, variant 1: c.9433C>T/p.L3145F, variant 2: c.13335_13347delinsCTTG/ p.E4445_S4449delinsDL - USH2A_001187 solved, compound heterozygous PubMed: Weisschuh 2020 - - Germline yes - - - - DNA SEQ blood Sanger sequencing retinal disease 241 PubMed: Weisschuh 2020 Filing key number: 82, autosomal recessive retinitis pigmentosa, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
?/. - c.9433C>T r.(?) p.(Leu3145Phe) - Parent #2 ACMG VUS g.215990476G>A g.215817134G>A USH2A c.9433C>T, p.(Leu3145Phe) - USH2A_001187 heterozygous PubMed: Reurink 2021 - - Unknown ? - - - - DNA SEQ-NG-I - molecular inversion probe-based sequencing retinal disease W19-0120 PubMed: Reurink 2021 genetically unexplained subjects from centers in the Netherlands, Ireland and Poland ? - Netherlands - - - - - 1 LOVD
?/. 48 c.9433C>T r.(?) p.(Leu3145Phe) - Parent #2 - VUS g.215990476G>A - c.9433C>T - USH2A_001187 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - M - - - - - - - 1 Daan Panneman
?/. 48 c.9433C>T r.(?) p.(Leu3145Phe) - Parent #1 - VUS g.215990476G>A - c.9433C>T - USH2A_001187 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing retinal disease - PubMed: Panneman 2023 - M - - - - - - - 1 Daan Panneman
?/. 48 c.9433C>T r.(?) p.(Leu3145Phe) - Parent #1 - VUS g.215990476G>A - c.9433C>T - USH2A_001187 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - F - - - - - - - 1 Daan Panneman
?/. 48 c.9433C>T r.(9433c>u) p.(Leu3145Phe) - Parent #2 ACMG VUS g.215990476G>A g.215817134G>A - - USH2A_001187 - PubMed: Reurink 2023, Journal: Reurink 2023 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease arRP24 PubMed: Reurink 2023, Journal: Reurink 2023 - - - - - - - - - 1 Janine Reurink
?/? 48 c.9433C>T r.(?) p.(Leu3145Phe) Fibronectin type-III 18 (3113 - 3209) Unknown ACMG VUS g.215990476G>A g.215817134G>A - - USH2A_001187 PM2_P, PM3_S following ClinGen GN005 - - rs267598373 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.9433C>T r.(?) p.(Leu3145Phe) - Unknown ACMG VUS g.215990476G>A g.215817134G>A - - USH2A_001187 ACMG GN005 criteria: PM2_P PM3_M PP1_M PubMed: Reurink, J. et al., 2021; PubMed: Weisschuh, N. et al., 2020 - rs267598373 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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