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.

11 entries on 1 page. Showing entries 1 - 11.
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Effect     

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+?/? 25 c.5012G>A r.(?) p.(Gly1671Asp) Laminin G-like 1 (1517-1709) Unknown ACMG VUS g.216258195C>T g.216084853C>T - - USH2A_000616 Heterozygous; Neutral PubMed: Le Quesne Stabej 2012, USMA missense analysis, missense variant in MSV3d - - Germline - - +Hpy166II;+HpyCH4III;-CviKI_1; - - DNA SEQ - - USH3 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+?/? 25 c.5012G>A r.(?) p.(Gly1671Asp) Laminin G-like 1 (1517-1709) Unknown ACMG VUS g.216258195C>T g.216084853C>T - - USH2A_000616 Heterozygous; Neutral PubMed: Le Quesne Stabej 2012, USMA missense analysis, missense variant in MSV3d - - Germline - - +Hpy166II;+HpyCH4III;-CviKI_1; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+?/. - c.5012G>A r.(?) p.(Gly1671Asp) - Parent #1 ACMG likely pathogenic g.216258195C>T - c.[12448A>G;5012G>A] - USH2A_000616 - PubMed: Sharon 2019 - - Germline - 1/2420 IRD families - - - DNA SEQ - - retinal disease - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - 1 Global Variome, with Curator vacancy
+/. - c.5012G>A r.(?) p.(Gly1671Asp) - Both (homozygous) - pathogenic (recessive) g.216258195C>T - 1:216258195C>T ENST00000307340.3:c.5012G>A (Gly1671Asp) - USH2A_000616 - PubMed: Carss 2017 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease G001367 PubMed: Carss 2017 - M - United Kingdom (Great Britain) Asia-South - - - - 1 LOVD
+/. - c.5012G>A r.(?) p.(Gly1671Asp) - Both (homozygous) - pathogenic (recessive) g.216258195C>T - 1:216258195C>T ENST00000307340.3:c.5012G>A (Gly1671Asp) - USH2A_000616 - PubMed: Carss 2017 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease G007281 PubMed: Carss 2017 - F - United Kingdom (Great Britain) Asia-South - - - - 1 LOVD
+/. - c.5012G>A r.(?) p.(Gly1671Asp) - Both (homozygous) - pathogenic g.216258195C>T g.216084853C>T - - USH2A_000616 - PubMed: Ge 2015 - - Germline - - - - - DNA SEQ-NG - 195-gene panel retinal disease JX+6.76 PubMed: Ge 2015 family - - United States - - - - - 1 LOVD
+/. - c.5012G>A r.(?) p.(Gly1671Asp) - Both (homozygous) - pathogenic g.216258195C>T g.216084853C>T - - USH2A_000616 - PubMed: Ge 2015 - - Germline - - - - - DNA SEQ-NG - 195-gene panel retinal disease 5ZU+U.41 PubMed: Ge 2015 simplex case - - United States - - - - - 1 LOVD
+?/. - c.5012G>A r.(?) p.(Gly1671Asp) - Both (homozygous) - likely pathogenic g.216258195C>T g.216084853C>T USH2A c.5012G>A, p.Gly1671Asp - USH2A_000616 homozygous PubMed: Turro 2020 - - Germline/De novo (untested) ? - - - - DNA SEQ-NG-I blood whole genome sequencing retinal disease G001367 PubMed: Turro 2020 only individuals with mutations in retinal disease genes from this publication were inserted into LOVD ? - (United Kingdom (Great Britain)) - - - - - 1 LOVD
+?/. - c.5012G>A r.(?) p.(Gly1671Asp) - Both (homozygous) - likely pathogenic g.216258195C>T g.216084853C>T USH2A c.5012G>A, p.Gly1671Asp - USH2A_000616 homozygous PubMed: Turro 2020 - - Germline/De novo (untested) ? - - - - DNA SEQ-NG-I blood whole genome sequencing retinal disease G007281 PubMed: Turro 2020 only individuals with mutations in retinal disease genes from this publication were inserted into LOVD ? - (United Kingdom (Great Britain)) - - - - - 1 LOVD
+?/. - c.5012G>A r.(?) p.(Gly1671Asp) - Unknown - likely pathogenic g.216258195C>T g.216084853C>T USH2A c.5012G>A, p.Gly1671Asp - USH2A_000616 heterozygous PubMed: Turro 2020 - - Germline/De novo (untested) ? - - - - DNA SEQ-NG-I blood whole genome sequencing retinal disease G005236 PubMed: Turro 2020 only individuals with mutations in retinal disease genes from this publication were inserted into LOVD ? - (United Kingdom (Great Britain)) - - - - - 1 LOVD
+/. - c.5012G>A r.(?) p.(Gly1671Asp) - Parent #1 - pathogenic g.216258195C>T g.216084853C>T - - USH2A_000616 - PubMed: Midgley 2024 - rs727505116 Germline - - - - - DNA SEQ-NG - gene panel retinal disease Pat53 PubMed: Midgley 2024 - F - South Africa India - - - - 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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