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.

18 entries on 1 page. Showing entries 1 - 18.
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Effect     

Exon     

AscendingDNA change (cDNA)     

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ClinVar ID     

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-/. - c.2522C>A r.(?) p.(Ser841Tyr) - Unknown - benign g.216420214G>T g.216246872G>T USH2A(NM_206933.2):c.2522C>A (p.S841Y), USH2A(NM_206933.4):c.2522C>A (p.S841Y) - USH2A_000184 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/. - c.2522C>A r.(?) p.(Ser841Tyr) - Unknown - benign g.216420214G>T g.216246872G>T USH2A(NM_206933.2):c.2522C>A (p.S841Y), USH2A(NM_206933.4):c.2522C>A (p.S841Y) - USH2A_000184 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/? 13 c.2522C>A r.(?) p.(Ser841Tyr) Laminin EGF-like 6 (795-846) Unknown ACMG likely benign g.216420214G>T g.216246872G>T - - USH2A_000184 Heterozygous; UV1 PubMed: Le Quesne Stabej 2012, USMA missense analysis, missense variant in MSV3d - rs111033282 Germline - 0/96 controls none - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/? 13 c.2522C>A r.(?) p.(Ser841Tyr) Laminin EGF-like 6 (795-846) Unknown ACMG likely benign g.216420214G>T g.216246872G>T - - USH2A_000184 Heterozygous PubMed: Jaijo 2010, USMA missense analysis, missense variant in MSV3d - rs111033282 Germline - - none - - DNA SEQ - - USH2 - PubMed: Jaijo 2010 Proband M - Spain - - - - - 1 Jose Maria Millan
-/- 13 c.2522C>A r.(?) p.(Ser841Tyr) Laminin EGF-like 6 (795-846) Unknown ACMG likely benign g.216420214G>T g.216246872G>T - - USH2A_000184 Heterozygous PubMed: Baux 2014, USMA missense analysis, missense variant in MSV3d - rs111033282 Germline - - none - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband M - France - - - - - 1 Anne-Françoise Roux
-/? 13 c.2522C>A r.(?) p.(Ser841Tyr) Laminin EGF-like 6 (795-846) Unknown ACMG likely benign g.216420214G>T g.216246872G>T - - USH2A_000184 Heterozygous; UV2 PubMed: Garcia-Garcia 2011, USMA missense analysis, missense variant in MSV3d - rs111033282 Germline - - none - - DNA SEQ - - ? - PubMed: Garcia-Garcia 2011 Proband M - Spain - - - - - 1 Jose Maria Millan
-?/. - c.2522C>A r.(?) p.(Ser841Tyr) - Unknown - likely benign g.216420214G>T g.216246872G>T USH2A(NM_206933.2):c.2522C>A (p.S841Y), USH2A(NM_206933.4):c.2522C>A (p.S841Y) - USH2A_000184 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.2522C>A r.(?) p.(Ser841Tyr) - Parent #1 - likely pathogenic g.216420214G>T - - - USH2A_000184 - PubMed: Holtan 2020 - - Germline - 10/899 cases - - - DNA SEQ - - retinal disease - PubMed: Holtan 2020 10 patients with variant in heterozygous or compound heterozygous form - - Norway - - - - - 10 Global Variome, with Curator vacancy
+/. - c.2522C>A r.(?) p.(Ser841Tyr) - Unknown - pathogenic (recessive) g.216420214G>T - 1:216420214G>T ENST00000307340.3:c.2522C>A (Ser841Tyr) - USH2A_000184 - PubMed: Carss 2017 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease G009000 PubMed: Carss 2017 - F - United Kingdom (Great Britain) Europe - - - - 1 LOVD
+/. 13 c.2522C>A r.(?) p.(Ser841Tyr) - Parent #1 - pathogenic g.216420214G>T g.216246872G>T - - USH2A_000184 unknown variant 2nd chromosome PubMed: Dad 2016 - - Germline - - - - - DNA PE - - retinal disease USH2-29 PubMed: Dad 2016 - M no Denmark - - - - - 1 LOVD
+?/. - c.2522C>A r.(?) p.(Ser841Tyr) - Unknown - likely pathogenic g.216420214G>T g.216246872G>T - - USH2A_000184 - PubMed: Ellingford 2016 - - Germline - - - - - DNA SEQ - 105-gene panel retinal disease 13011433 PubMed: Ellingford 2016 familial segregation analysis requested - - - - - - - - 1 LOVD
+?/. - c.2522C>A r.(?) p.(Ser841Tyr) - Unknown - likely pathogenic g.216420214G>T g.216246872G>T - - USH2A_000184 - PubMed: Ellingford 2016 - - Germline - - - - - DNA SEQ - 105-gene panel retinal disease 13005697 PubMed: Ellingford 2016 patient - - - - - - - - 1 LOVD
+?/. - c.2522C>A r.(?) p.(Ser841Tyr) - Unknown - likely pathogenic g.216420214G>T g.216246872G>T - - USH2A_000184 - PubMed: Ellingford 2016 - - Germline - - - - - DNA SEQ - 105-gene panel retinal disease 12012730 PubMed: Ellingford 2016 patient - - - - - - - - 1 LOVD
+/. - c.2522C>A r.(?) p.(Ser841Tyr) - Unknown - pathogenic g.216420214G>T g.216246872G>T - - USH2A_000184 no variant 2nd chromosome PubMed: Neuhaus 2017 - rs111033282 Germline - - - - - DNA SEQ, SEQ-NG - gene panel USH Pat29 PubMed: Neuhaus 2017 - - no Germany - - - - - 1 LOVD
?/. - c.2522C>A r.(?) p.(Ser841Tyr) - Unknown ACMG VUS g.216420214G>T g.216246872G>T USH2A c.2522C>A, p.(Ser841Tyr), c.5975A>G, p.(Tyr1992Cys) - USH2A_000184 - PubMed: Jespersgaar 2019 - - Germline ? - - - - DNA SEQ-NG-I blood 125 genes associated with inherited retinal disorders, see paper supplemental data retinal disease 482 PubMed: Jespersgaar 2019 - ? - Denmark - - - - - 1 LOVD
+?/. - c.2522C>A r.(?) p.(Ser841Tyr) - Unknown - likely pathogenic g.216420214G>T g.216246872G>T USH2A c.2522C>A, p.Ser841Tyr - USH2A_000184 heterozygous PubMed: Turro 2020 - - Germline/De novo (untested) ? - - - - DNA SEQ-NG-I blood whole genome sequencing retinal disease G009000 PubMed: Turro 2020 only individuals with mutations in retinal disease genes from this publication were inserted into LOVD ? - - - - - - - 1 LOVD
-/. 13 c.2522C>A r.(2522c>a) p.(Ser841Tyr) - Parent #1 ACMG benign g.216420214G>T g.216246872G>T - - USH2A_000184 no variant 2nd chromome PubMed: Reurink 2023, Journal: Reurink 2023 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease arRP39 PubMed: Reurink 2023, Journal: Reurink 2023 - - - - - - - - - 1 Janine Reurink
?/. - c.2522C>A r.(?) p.(Ser841Tyr) - Unknown ACMG VUS g.216420214G>T g.216246872G>T - - USH2A_000184 ACMG PM2 PubMed: Weisschuh 2024 - - Germline - - - - - DNA SEQ-NG - WGS ? SRP-907 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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