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.

13 entries on 1 page. Showing entries 1 - 13.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

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DNA change (hg38)     

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DB-ID     

Variant remarks     

Reference     

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Disease     

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Owner     
-/. - c.5975A>G r.(?) p.(Tyr1992Cys) - Unknown - benign g.216243517T>C g.216070175T>C USH2A(NM_206933.2):c.5975A>G (p.Y1992C), USH2A(NM_206933.4):c.5975A>G (p.Y1992C) - USH2A_000415 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/? 30 c.5975A>G r.(?) p.(Tyr1992Cys) Fibronectin type-III 6 (1954-2051) Unknown ACMG likely benign g.216243517T>C g.216070175T>C - - USH2A_000415 Heterozygous; UV1 PubMed: Le Quesne Stabej 2012, USMA missense analysis, missense variant in MSV3d - rs41303287 Germline - 1/96 controls none - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-?/? 30 c.5975A>G r.(?) p.(Tyr1992Cys) Fibronectin type-III 6 (1954-2051) Unknown ACMG likely benign g.216243517T>C g.216070175T>C - - USH2A_000415 Heterozygous; possibly deleterious PubMed: McGee 2010, USMA missense analysis, missense variant in MSV3d - rs41303287 Germline - - none - - DNA SEQ - - USH2 - PubMed: McGee 2010 Proband - No genotype in the publication - - United States - - - - - 2 Anne-Françoise Roux
-?/? 30 c.5975A>G r.(?) p.(Tyr1992Cys) Fibronectin type-III 6 (1954-2051) Parent #1 ACMG likely benign g.216243517T>C g.216070175T>C - - USH2A_000415 Heterozygous; UV3 PubMed: Garcia-Garcia 2011, USMA missense analysis, missense variant in MSV3d - rs41303287 Germline - - none - - DNA SEQ - - ? - PubMed: Garcia-Garcia 2011 Proband M - Spain - - - - - 1 Jose Maria Millan
-?/? 30 c.5975A>G r.(?) p.(Tyr1992Cys) Fibronectin type-III 6 (1954-2051) Unknown ACMG likely benign g.216243517T>C g.216070175T>C - - USH2A_000415 Heterozygous; likely polymorphism PubMed: Vastinsalo 2012, USMA missense analysis, missense variant in MSV3d - rs41303287 Germline - - none - - DNA PE, SEQ - APEX USH1 - PubMed: Vastinsalo 2012 Proband - - Finland - - - - - 1 Anne-Françoise Roux
-?/? 30 c.5975A>G r.(?) p.(Tyr1992Cys) Fibronectin type-III 6 (1954-2051) Unknown ACMG likely benign g.216243517T>C g.216070175T>C - - USH2A_000415 Heterozygous; mutation PubMed: Krawitz 2014, USMA missense analysis, missense variant in MSV3d - rs41303287 Germline - - none - - DNA SEQ-NG-S - - USH2 - PubMed: Krawitz 2014 Proband F - Germany - - - - - 1 Peter Krawitz
-?/. - c.5975A>G r.(?) p.(Tyr1992Cys) - Unknown - likely benign g.216243517T>C g.216070175T>C USH2A(NM_206933.2):c.5975A>G (p.Y1992C), USH2A(NM_206933.4):c.5975A>G (p.Y1992C) - USH2A_000415 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.5975A>G r.(?) p.(Tyr1992Cys) - Unknown - likely benign g.216243517T>C g.216070175T>C USH2A(NM_206933.2):c.5975A>G (p.Y1992C), USH2A(NM_206933.4):c.5975A>G (p.Y1992C) - USH2A_000415 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.5975A>G r.(?) p.(Tyr1992Cys) - Parent #1 - likely pathogenic g.216243517T>C - - - USH2A_000415 - PubMed: Holtan 2020 - - Germline - 4/899 cases - - - DNA SEQ - - retinal disease - PubMed: Holtan 2020 4 patients with variant in heterozygous or compound heterozygous form - - Norway - - - - - 4 Global Variome, with Curator vacancy
+?/. - c.5975A>G r.(?) p.(Tyr1992Cys) - Unknown - likely pathogenic g.216243517T>C g.216070175T>C - - USH2A_000415 - PubMed: Ellingford 2016 - - Germline - - - - - DNA SEQ - 105-gene panel retinal disease 13011433 PubMed: Ellingford 2016 familial segregation analysis requested - - - - - - - - 1 LOVD
?/. - c.5975A>G r.(?) p.(Tyr1992Cys) - Unknown ACMG VUS g.216243517T>C g.216070175T>C USH2A c.2522C>A, p.(Ser841Tyr), c.5975A>G, p.(Tyr1992Cys) - USH2A_000415 - 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
+?/. 30 c.5975A>G r.(?) p.(Tyr1992Cys) - Unknown - likely pathogenic g.216243517T>C - c.5975A>G - USH2A_000415 - PubMed: Booij-2011 - rs41303287 Germline - - - - - DNA arraySEQ Blood - retinal disease - PubMed: Booij-2011 - - - - - - - - - 1 LOVD
-/. - c.5975A>G r.(?) p.(Tyr1992Cys) - Unknown ACMG benign g.216243517T>C g.216070175T>C - - USH2A_000415 ACMG GN005 criteria: BS1_S BS2_S PubMed: Garcia-Garcia, G. et al., 2011 - rs41303287 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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