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.

5 entries on 1 page. Showing entries 1 - 5.
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+?/? 62 c.12284G>A r.(=) p.(Gly4095Asp) Fibronectin type-III 26 (4066-4150) Unknown ACMG VUS g.215853501C>T g.215680159C>T - - USH2A_000846 Heterozygous; mutation PubMed: Krawitz 2014, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ-NG-S - - USH2 - PubMed: Krawitz 2014 Proband F - Germany - - - - - 1 Peter Krawitz
+?/? 62 c.12284G>A r.(?) p.(Gly4095Asp) Fibronectin type-III 26 (4066-4150) Parent #2 ACMG VUS g.215853501C>T g.215680159C>T - - USH2A_000846 Heterozygous; mutation PubMed: Bonnet 2016, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband - - Slovenia - - - - - 1 Crystel Bonnet
+?/. - c.12284G>A r.(?) p.(Gly4095Asp) - Parent #1 - likely pathogenic g.215853501C>T g.215680159C>T USH2A, variant 1: c.9921T>G/p.C3307W, variant 2: c.12284G>A/p.G4095D - USH2A_000846 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET8 targeted sequencing panel - see paper retinal disease 946 PubMed: Weisschuh 2020 Filing key number: 419, sporadic retinitis pigmentosa, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
+?/. 62 c.12284G>A r.(?) p.(Gly4095Asp) - Parent #1 ACMG likely pathogenic g.215853501C>T g.215680159C>T USH2A c.G12284A, p.G4095D - USH2A_000846 - PubMed: Zhu 2021 - - Germline yes - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease HSR505 PubMed: Zhu 2021 family 177, patient HSR505 F - China - - - - - 1 LOVD
?/. - c.12284G>A r.(?) p.(Gly4095Asp) - Unknown ACMG VUS g.215853501C>T g.215680159C>T - - USH2A_000846 ACMG GN005 criteria: PM2_P PM3_P PP3_P PubMed: Bonnet, C. et al., 2016; PubMed: Weisschuh, N. et al., 2020 - rs759898765 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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