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.

7 entries on 1 page. Showing entries 1 - 7.
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-?/. - c.2546G>A r.(?) p.(Cys849Tyr) - Unknown - likely benign g.216420190C>T g.216246848C>T USH2A(NM_206933.2):c.2546G>A (p.C849Y), USH2A(NM_206933.4):c.2546G>A (p.C849Y) - USH2A_000306 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.2546G>A r.(?) p.(Cys849Tyr) - Unknown - likely benign g.216420190C>T g.216246848C>T USH2A(NM_206933.2):c.2546G>A (p.C849Y), USH2A(NM_206933.4):c.2546G>A (p.C849Y) - USH2A_000306 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/- 13 c.2546G>A r.(?) p.(Cys849Tyr) Laminin EGF-like 7 (847-899) Unknown - benign g.216420190C>T g.216246848C>T - - USH2A_000306 Heterozygous; previously reported as UV4 but reclassified based on MAF (see gnomAD for instance) PubMed: Baux 2014, USMA missense analysis, missense variant in MSV3d - rs111033481 Germline - - - - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband M - Cameroon - - - - - 1 Anne-Françoise Roux
?/. - c.2546G>A r.(?) p.(Cys849Tyr) - Unknown - VUS g.216420190C>T g.216246848C>T - - USH2A_000306 - PubMed: Wang 2014 - rs111033481 Germline - - - - - DNA SEQ-NG - 66-gene panel retinal disease 64 PubMed: Wang 2014 - F - United States - - - - - 1 LOVD
+?/. - c.2546G>A r.(?) p.(Cys849Tyr) - Parent #1 - likely pathogenic g.216420190C>T g.216246848C>T USH2A, variant 1: c.14650G>T/p.E4884*, variant 2: c.2546G>A/p.C849Y - USH2A_000306 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET6 targeted sequencing panel - see paper retinal disease 1148 PubMed: Weisschuh 2020 Filing key number: 811, sporadic retinitis pigmentosa, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
+?/. 13 c.2546G>A r.(?) p.(Cys849Tyr) - Unknown - likely pathogenic g.216420190C>T - p.C849Y - USH2A_000306 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
-/. - c.2546G>A r.(?) p.(Cys849Tyr) - Unknown ACMG benign g.216420190C>T g.216246848C>T - - USH2A_000306 ACMG GN005 criteria: PP3_P BS1_S BS2_S PubMed: Wafa, T. T. et al., 2021; PubMed: Weisschuh, N. et al., 2020; PubMed: Sloan-Heggen, C. M. et al., 2016 - rs111033481 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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