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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+?/? 33 c.6383G>A r.(?) p.(Cys2128Tyr) Fibronectin type-III 7 (2052-2138) Unknown ACMG VUS g.216173847C>T g.216000505C>T - - USH2A_000417 Heterozygous; likely deleterious PubMed: McGee 2010, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ - - USH2 - PubMed: McGee 2010 Proband - No genotype in the publication - - United States - - - - - 1 Anne-Françoise Roux
+?/? 33 c.6383G>A r.(?) p.(Cys2128Tyr) Fibronectin type-III 7 (2052-2138) Parent #2 ACMG VUS g.216173847C>T g.216000505C>T - - USH2A_000417 Heterozygous; likely deleterious PubMed: Bonnet 2016, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband F - Germany - - - - - 1 Crystel Bonnet
+/. 33 c.6383G>A r.(?) p.(Cys2128Tyr) - Unknown ACMG pathogenic g.216173847C>T g.216000505C>T NM_206933.2:c.6383G>A, NP_996816.2:p.(Cys2128Tyr), NC_000001.10:g.216173847C>T - USH2A_000417 - PubMed: Wang 2018 - - Germline ? - - - - DNA SEQ-NG - exome sequencing retinal disease 2016101023 PubMed: Wang 2018 - M ? China Han Chinese - - - - 1 LOVD
+?/. - c.6383G>A r.(?) p.(Cys2128Tyr) - Parent #1 - likely pathogenic g.216173847C>T g.216000505C>T USH2A, variant 1: c.6383G>A/p.C2128Y, variant 2: c.8834G>A/p.W2945* - USH2A_000417 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET3 targeted sequencing panel - see paper retinal disease 550 PubMed: Weisschuh 2020 Filing key number: 195, Usher syndrome type 2, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
+?/. 33 c.6383G>A r.(?) p.(Cys2128Tyr) - Unknown - likely pathogenic (recessive) g.216173847C>T - c.6383G>A - USH2A_000417 - PubMed: Liu-2020 - - Germline - - - - - DNA SEQ-NG - WES retinal disease - PubMed: Liu-2020 - M - - - - - - - 1 LOVD
?/. - c.6383G>A r.(?) p.(Cys2128Tyr) - Unknown ACMG VUS g.216173847C>T g.216000505C>T - - USH2A_000417 ACMG GN005 criteria: PM2_P PM3_M PubMed: Bonnet, C. et al., 2016; PubMed: Weisschuh, N. et al., 2020 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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