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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?/. - c.6670G>T r.(?) p.(Gly2224Cys) - Unknown - VUS g.216166497C>A g.215993155C>A USH2A(NM_206933.2):c.6670G>T (p.G2224C) - USH2A_001624 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.6670G>T r.(?) p.(Gly2224Cys) - Unknown - VUS g.216166497C>A - USH2A(NM_206933.2):c.6670G>T (p.G2224C) - USH2A_001624 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.6670G>T r.(?) p.(Gly2224Cys) - Unknown - pathogenic (recessive) g.216166497C>A - 1:216166497C>A ENST00000307340.3:c.6670G>T (Gly2224Cys) - USH2A_001624 - PubMed: Carss 2017 - - Germline - - - - - DNA SEQ-NG - WES retinal disease B240237 PubMed: Carss 2017 - M - United Kingdom (Great Britain) - - - - - 1 LOVD
+?/. - c.6670G>T r.(?) p.(Gly2224Cys) - Unknown - likely pathogenic (recessive) g.216166497C>A - 1:216166497C>A ENST00000307340.3:c.6670G>T (Gly2224Cys) - USH2A_001624 - PubMed: Carss 2017 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease G005495 PubMed: Carss 2017 - M - United Kingdom (Great Britain) Europe - - - - 1 LOVD
+?/. - c.6670G>T r.(?) p.(Gly2224Cys) - Unknown - likely pathogenic g.216166497C>A g.215993155C>A - - USH2A_001624 - PubMed: Stone 2017 - - Germline - - - - - DNA SEQ-NG - - retinal disease 105 PubMed: Stone 2017 1 affected F - (United States) - - - - - 1 LOVD
+/. - c.6670G>T r.(?) p.(Gly2224Cys) - Parent #2 - pathogenic g.216166497C>A g.215993155C>A - - USH2A_001624 - PubMed: Khan 2017 - - Germline - - - - - DNA SEQ-NG - 105-gene panel retinal disease 27978 PubMed: Khan 2017 see paper - - United Kingdom (Great Britain) - - - - - 1 LOVD
+/. - c.6670G>T r.(?) p.(Gly2224Cys) - Parent #2 - pathogenic (recessive) g.216166497C>A g.215993155C>A - - USH2A_001624 - PubMed: Consugar 2015 - - Germline yes - - - - DNA SEQ-NG - 238-gene panel retinal disease OGI-546-1114 PubMed: Consugar 2015 - - - United States - - - - - 1 LOVD
+?/. 35 c.6670G>T r.(?) p.(Gly2224Cys) - Unknown - likely pathogenic g.216166497C>A g.215993155C>A USH2A Ex.35 c.6670G>T p.(Gly2224Cys), Ex.44 c.8725G>A p.(Gly2909Ser) - USH2A_001624 compound heterozygous PubMed: Martin Merida 2019 - - Germline/De novo (untested) ? - - - - DNA SEQ-NG-I - - retinal disease RP-2083 PubMed: Martin Merida 2019 - ? - Spain - - - - - 1 LOVD
+?/. - c.6670G>T r.(?) p.(Gly2224Cys) - Unknown - likely pathogenic g.216166497C>A g.215993155C>A USH2A;NM_206933.2;c.[6670G>T];[10342G>A];p.[(Gly2224Cys)];[(Glu3448Lys)] - USH2A_001624 compound heterozygous PubMed: Jiman 2020 - - Unknown ? - - - - DNA SEQ-NG-I - 105 genes panel retinal disease 69 PubMed: Jiman 2020 - M - (United Kingdom (Great Britain)) - - - - - 1 LOVD
?/. - c.6670G>T r.(?) p.(Gly2224Cys) - Unknown - VUS g.216166497C>A g.215993155C>A USH2A c.6670G>T, p.Gly2224Cys - USH2A_001624 This variant is likely in cis with the above missense variant, heterozygous PubMed: Zampaglione 2020 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ blood - retinal disease 039-207 PubMed: Zampaglione 2020 - ? - - - - - - - 1 LOVD
+?/. - c.6670G>T r.(?) p.(Gly2224Cys) - Parent #1 - likely pathogenic g.216166497C>A g.215993155C>A USH2A, variant 1: c.2299del/p.E767Sfs*21, variant 2: c.6670G>T/p.G2224C - USH2A_001624 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET3 targeted sequencing panel - see paper retinal disease 950 PubMed: Weisschuh 2020 Filing key number: 422, sporadic retinitis pigmentosa, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
?/. 35 c.6670G>T r.(?) p.(Gly2224Cys) - Parent #1 - VUS g.216166497C>A - c.6670G>T - USH2A_001624 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - M - - - - - - - 1 Daan Panneman
?/. 35 c.6670G>T r.(6670g>u) p.(Gly2224Cys) - Parent #1 ACMG VUS g.216166497C>A g.215993155C>A - - USH2A_001624 - PubMed: Reurink 2023, Journal: Reurink 2023 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease USH6 PubMed: Reurink 2023, Journal: Reurink 2023 - - - - - - - - - 1 Janine Reurink
?/. - c.6670G>T r.(?) p.(Gly2224Cys) - Unknown ACMG VUS g.216166497C>A g.215993155C>A - - USH2A_001624 ACMG GN005 criteria: PubMed: Weisschuh, N. et al., 2020 - rs149553844 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.6670G>T r.(?) p.(Gly2224Cys) - Unknown ACMG VUS g.216166497C>A g.215993155C>A - - USH2A_001624 ACMG PM2, PP5 PubMed: Weisschuh 2024 - - Germline - - - - - DNA SEQ-NG - WGS ? SRP-670 PubMed: Weisschuh 2024 patient, no family history M - 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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