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.

6 entries on 1 page. Showing entries 1 - 6.
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+?/? 50 c.9921T>G r.(?) p.(Cys3307Trp) Cystein rich (3192-3358) Unknown ACMG VUS g.215972286A>C g.215798944A>C - - USH2A_000544 Heterozygous; Presumably pathogenic PubMed: Bonnet 2011, USMA missense analysis, missense variant in MSV3d - - Germline - 0/482 controls none - - DNA SEQ - - USH1 - PubMed: Bonnet 2011 Proband - - - - - - - - 1 Anne-Françoise Roux
+/. - c.9921T>G r.(?) p.(Cys3307Trp) - Parent #1 - pathogenic g.215972286A>C g.215798944A>C - - USH2A_000544 - PubMed: Ge 2015 - - Germline - - - - - DNA SEQ-NG - 195-gene panel retinal disease 5FV+T.56 PubMed: Ge 2015 simplex case - - United States - - - - - 1 LOVD
+?/. - c.9921T>G r.(?) p.(Cys3307Trp) - Parent #1 - likely pathogenic g.215972286A>C g.215798944A>C USH2A, variant 1: c.9921T>G/p.C3307W, variant 2: c.12284G>A/p.G4095D - USH2A_000544 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
?/. 50 c.9921T>G r.(?) p.(Cys3307Trp) - Parent #2 - VUS g.215972286A>C - c.9921T>G - USH2A_000544 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - F - - - - - - - 1 Daan Panneman
?/. 50 c.9921T>G r.(?) p.(Cys3307Trp) - Both (homozygous) - VUS g.215972286A>C - c.9921T>G - USH2A_000544 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - M - - - - - - - 1 Daan Panneman
?/. - c.9921T>G r.(?) p.(Cys3307Trp) - Unknown ACMG VUS g.215972286A>C g.215798944A>C - - USH2A_000544 ACMG GN005 criteria: PM2_P PubMed: Weisschuh, N. et al., 2020 - rs1057519382 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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