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.

12 entries on 1 page. Showing entries 1 - 12.
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Effect     

Exon     

AscendingDNA change (cDNA)     

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-?/. - c.7685T>C r.(?) p.(Val2562Ala) - Unknown - likely benign g.216062306A>G g.215888964A>G USH2A(NM_206933.2):c.7685T>C (p.V2562A) - USH2A_000266 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/? 41 c.7685T>C r.(?) p.(Val2562Ala) Fibronectin type-III 12 (2533-2619) Paternal (confirmed) ACMG likely benign g.216062306A>G g.215888964A>G - - USH2A_000266 Heterozygous PubMed: Vastinsalo 2012, USMA missense analysis, missense variant in MSV3d - rs56385601 Germline - 0.6% (150 controls) +CviKI_1 - - DNA PE, SEQ - APEX USH3 - PubMed: Vastinsalo 2012 Proband F - Finland - - - - - 1 Anne-Françoise Roux
-?/? 41 c.7685T>C r.(?) p.(Val2562Ala) Fibronectin type-III 12 (2533-2619) Parent #1 ACMG likely benign g.216062306A>G g.215888964A>G - - USH2A_000266 Heterozygous PubMed: Jaijo 2010, USMA missense analysis, missense variant in MSV3d - rs56385601 Germline - - +CviKI_1 - - DNA SEQ - - USH2 - PubMed: Jaijo 2010 Proband M - Spain - - - - - 1 Jose Maria Millan
-?/? 41 c.7685T>C r.(?) p.(Val2562Ala) Fibronectin type-III 12 (2533-2619) Paternal (confirmed) ACMG likely benign g.216062306A>G g.215888964A>G - - USH2A_000266 Heterozygous PubMed: Baux 2014, USMA missense analysis, missense variant in MSV3d - rs56385601 Germline - - +CviKI_1 - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband F - France - - - - - 1 Anne-Françoise Roux
-?/? 41 c.7685T>C r.(?) p.(Val2562Ala) Fibronectin type-III 12 (2533-2619) Parent #2 ACMG likely benign g.216062306A>G g.215888964A>G - - USH2A_000266 Heterozygous PubMed: Le Guédard-Méreuze 2010, USMA missense analysis, missense variant in MSV3d - rs56385601 Germline - - +CviKI_1 - - DNA minigene, SEQ - - USH2 - PubMed: Le Guédard-Méreuze 2010 Proband M - France - - - - - 1 Anne-Françoise Roux
-?/? 41 c.7685T>C r.(?) p.(Val2562Ala) Fibronectin type-III 12 (2533-2619) Unknown ACMG likely benign g.216062306A>G g.215888964A>G - - USH2A_000266 Heterozygous; benign PubMed: McGee 2010, USMA missense analysis, missense variant in MSV3d - rs56385601 Germline - - +CviKI_1 - - DNA SEQ - - USH2 - PubMed: McGee 2010 Proband - No genotype in the publication - - United States - - - - - 1 Anne-Françoise Roux
-?/? 41 c.7685T>C r.(?) p.(Val2562Ala) Fibronectin type-III 12 (2533-2619) Unknown ACMG likely benign g.216062306A>G g.215888964A>G - - USH2A_000266 Heterozygous; benign PubMed: McGee 2010, USMA missense analysis, missense variant in MSV3d - rs56385601 Germline - - +CviKI_1 - - DNA SEQ - - RPar - PubMed: McGee 2010 Proband - No genotype in the publication - - United States - - - - - 4 Anne-Françoise Roux
-?/? 41 c.7685T>C r.(?) p.(Val2562Ala) Fibronectin type-III 12 (2533-2619) Unknown ACMG likely benign g.216062306A>G g.215888964A>G - - USH2A_000266 Heterozygous PubMed: Baux 2014, USMA missense analysis, missense variant in MSV3d - rs56385601 Germline - - +CviKI_1 - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband F - France - - - - - 1 Anne-Françoise Roux
-/? 41 c.7685T>C r.(?) p.(Val2562Ala) Fibronectin type-III 12 (2533-2619) Unknown ACMG likely benign g.216062306A>G g.215888964A>G - - USH2A_000266 Heterozygous PubMed: Baux 2014, USMA missense analysis, missense variant in MSV3d - rs56385601 Germline - - +CviKI_1 - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband M - France - - - - - 1 Anne-Françoise Roux
-?/. - c.7685T>C r.(?) p.(Val2562Ala) - Unknown - likely benign g.216062306A>G g.215888964A>G USH2A(NM_206933.2):c.7685T>C (p.V2562A) - USH2A_000266 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.7685T>C r.(?) p.(Val2562Ala) - Unknown - likely pathogenic g.216062306A>G g.215888964A>G c.4222C>T p.(Gln1408*), c.13576C>T p.(Arg4526*), c.7685T>C p.(Val2562Ala) - USH2A_000266 - PubMed: Hagag 2020 - - Germline/De novo (untested) ? - - - - DNA ? - - retinal disease Subject 032 PubMed: Hagag 2020 - ? - - - - - - - 1 LOVD
-?/. - c.7685T>C r.(?) p.(Val2562Ala) - Unknown - likely benign g.216062306A>G g.215888964A>G - - USH2A_000266 - PubMed: Eisenberger 2018 - rs56385601 Germline - - - - - DNA SEQ-NG-I - - DFNA FamPatIV2 PubMed: Eisenberger 2018 4-generation family, 8 affected (4F, 4M) M no Germany white - - - - 8 Hanno Bolz
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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