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.

19 entries on 1 page. Showing entries 1 - 19.
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Effect     

Exon     

AscendingDNA change (cDNA)     

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-?/. - c.6240G>T r.(?) p.(Lys2080Asn) - Unknown - likely benign g.216219858C>A g.216046516C>A USH2A(NM_206933.2):c.6240G>T (p.K2080N), USH2A(NM_206933.4):c.6240G>T (p.K2080N) - USH2A_000122 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/? 32 c.6240G>T r.(?) p.(Lys2080Asn) Fibronectin type-III 7 (2052-2138) Parent #1 ACMG likely benign g.216219858C>A g.216046516C>A - - USH2A_000122 Heterozygous PubMed: Baux 2007, USMA missense analysis, missense variant in MSV3d - rs114402911 Germline - - +HpyCH4V - - DNA SEQ - - USH2 - PubMed: Baux 2007 Proband F - France - - - - - 1 Anne-Françoise Roux
-/? 32 c.6240G>T r.(?) p.(Lys2080Asn) Fibronectin type-III 7 (2052-2138) Unknown ACMG likely benign g.216219858C>A g.216046516C>A - - USH2A_000122 Heterozygous; benign PubMed: McGee 2010, USMA missense analysis, missense variant in MSV3d - rs114402911 Germline - - +HpyCH4V - - DNA SEQ - - USH2 - PubMed: McGee 2010 Proband - No genotype in the publication - - United States - - - - - 1 Anne-Françoise Roux
-/? 32 c.6240G>T r.(?) p.(Lys2080Asn) Fibronectin type-III 7 (2052-2138) Unknown ACMG likely benign g.216219858C>A g.216046516C>A - - USH2A_000122 Heterozygous; benign PubMed: McGee 2010, USMA missense analysis, missense variant in MSV3d - rs114402911 Germline - - +HpyCH4V - - DNA SEQ - - RPar - PubMed: McGee 2010 Proband - No genotype in the publication - - United States - - - - - 1 Anne-Françoise Roux
-/? 32 c.6240G>T r.(?) p.(Lys2080Asn) Fibronectin type-III 7 (2052-2138) Unknown ACMG likely benign g.216219858C>A g.216046516C>A - - USH2A_000122 Heterozygous; Predicted benign PubMed: Neveling 2012, USMA missense analysis, missense variant in MSV3d - rs114402911 Germline - - +HpyCH4V - - DNA SEQ, SEQ-NG-S - - RPar - PubMed: Neveling 2012 Proband F - - - - - - - 1 Anne-Françoise Roux
-?/? 32 c.6240G>T r.(?) p.(Lys2080Asn) Fibronectin type-III 7 (2052-2138) Unknown ACMG likely benign g.216219858C>A g.216046516C>A - - USH2A_000122 Heterozygous PubMed: Baux 2014, USMA missense analysis, missense variant in MSV3d - rs114402911 Germline - - +HpyCH4V - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband M - France - - - - - 1 Anne-Françoise Roux
-/? 32 c.6240G>T r.(?) p.(Lys2080Asn) Fibronectin type-III 7 (2052-2138) Unknown ACMG likely benign g.216219858C>A g.216046516C>A - - USH2A_000122 Heterozygous PubMed: Baux 2014, USMA missense analysis, missense variant in MSV3d - rs114402911 Germline - - +HpyCH4V - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband M - France - - - - - 1 Anne-Françoise Roux
-/. - c.6240G>T r.(?) p.(Lys2080Asn) - Unknown - benign g.216219858C>A g.216046516C>A USH2A(NM_206933.2):c.6240G>T (p.K2080N), USH2A(NM_206933.4):c.6240G>T (p.K2080N) - USH2A_000122 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.6240G>T r.(?) p.(Lys2080Asn) - Parent #1 - likely pathogenic g.216219858C>A - - - USH2A_000122 - PubMed: Holtan 2020 - - Germline - 7/899 cases - - - DNA SEQ - - retinal disease - PubMed: Holtan 2020 7 patients with variant in heterozygous or compound heterozygous form - - Norway - - - - - 7 Global Variome, with Curator vacancy
+?/. - c.6240G>T r.(?) p.(Lys2080Asn) - Both (homozygous) - likely pathogenic (recessive) g.216219858C>A - - - USH2A_000122 - PubMed: Holtan 2020 - - Germline - 1/899 cases - - - DNA SEQ - - retinal disease - PubMed: Holtan 2020 1 homozygous patient - - Norway - - - - - 1 Global Variome, with Curator vacancy
+?/. - c.6240G>T r.(?) p.(Lys2080Asn) - Unknown - likely pathogenic (recessive) g.216219858C>A - 1:216219858C>A ENST00000307340.3:c.6240G>T (Lys2080Asn) - USH2A_000122 - PubMed: Carss 2017 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease G007671 PubMed: Carss 2017 - M - United Kingdom (Great Britain) Europe - - - - 1 LOVD
-/. - c.6240G>T r.(?) p.(Lys2080Asn) - Unknown - benign g.216219858C>A - USH2A(NM_206933.2):c.6240G>T (p.K2080N), USH2A(NM_206933.4):c.6240G>T (p.K2080N) - USH2A_000122 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.6240G>T r.(?) p.(Lys2080Asn) - Unknown - VUS g.216219858C>A g.216046516C>A - - USH2A_000122 - PubMed: Tiwari 2016 - - Germline - - - - - DNA SEQ-NG - WES retinal disease Case70946 PubMed: Tiwari 2016 see paper F - Switzerland - - - - - 1 LOVD
+/. - c.6240G>T r.(?) p.(Lys2080Asn) - Parent #1 - pathogenic (recessive) g.216219858C>A g.216046516C>A - - USH2A_000122 - PubMed: Consugar 2015 - - Germline yes - - - - DNA SEQ-NG - 238-gene panel retinal disease OGI-021-053 PubMed: Consugar 2015 - - - United States - - - - - 1 LOVD
?/. - c.6240G>T r.(?) p.(Lys2080Asn) - Unknown - VUS g.216219858C>A g.216046516C>A - - USH2A_000122 - PubMed: Wang 2014 - rs114402911 Germline - - - - - DNA SEQ-NG - 66-gene panel retinal disease 10 PubMed: Wang 2014 - M - United States - - - - - 1 LOVD
?/. - c.6240G>T r.(?) p.(Lys2080Asn) - Unknown - VUS g.216219858C>A g.216046516C>A - - USH2A_000122 - PubMed: Wang 2014 - rs114402911 Germline - - - - - DNA SEQ-NG - 66-gene panel retinal disease 60 PubMed: Wang 2014 - F - United States - - - - - 1 LOVD
+?/. 32 c.6240G>T r.(?) p.(Lys2080Asn) - Unknown - likely pathogenic g.216219858C>A - c.6240G>T - USH2A_000122 - PubMed: Booij-2011 - - Germline - - - - - DNA arraySEQ Blood - retinal disease - PubMed: Booij-2011 - - - - - - - - - 1 LOVD
-/. 32 c.6240G>T r.(6240g>u) p.(Lys2080Asn) - Parent #1 ACMG benign g.216219858C>A g.216046516C>A - - USH2A_000122 no variant 2nd chromome PubMed: Reurink 2023, Journal: Reurink 2023 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease arRP9 PubMed: Reurink 2023, Journal: Reurink 2023 - - - - - - - - - 1 Janine Reurink
-/. 32 c.6240G>T r.(6240g>u) p.(Lys2080Asn) - Parent #2 ACMG benign g.216219858C>A g.216046516C>A - - USH2A_000122 - PubMed: Reurink 2023, Journal: Reurink 2023 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease arRP25 PubMed: Reurink 2023, Journal: Reurink 2023 - - - - - - - - - 1 Janine Reurink
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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