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.

9 entries on 1 page. Showing entries 1 - 9.
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+?/? 8 c.1531G>A r.(?) p.(Glu511Lys) Laminin N-terminal (271-517) Unknown ACMG VUS g.216496835C>T g.216323493C>T - - USH2A_000529 Heterozygous PubMed: Baux 2014, USMA missense analysis, missense variant in MSV3d - - Germline - 0/184 controls none - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband M - France - - - - - 1 Anne-Françoise Roux
+?/? 8 c.1531G>A r.(?) p.(Glu511Lys) Laminin N-terminal (271-517) Unknown ACMG VUS g.216496835C>T g.216323493C>T - - USH2A_000529 Heterozygous PubMed: Baux 2014, USMA missense analysis, missense variant in MSV3d - - Germline - 0/184 controls none - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband F - France - - - - - 1 Anne-Françoise Roux
+?/? 8 c.1531G>A r.(?) p.(Glu511Lys ) Laminin N-terminal (271-517) Parent #1 ACMG VUS g.216496835C>T g.216323493C>T - - USH2A_000529 Heterozygous PubMed: Bonnet 2016, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband F - France - - - - - 1 Crystel Bonnet
+/. - c.1531G>A r.(?) p.(Glu511Lys) - Parent #2 - pathogenic (recessive) g.216496835C>T g.216323493C>T - - USH2A_000529 - PubMed: Fuster-Garcia 2018 - - Germline - - - - - DNA arraySEQ - - retinal disease RP971 PubMed: Fuster-Garcia 2018 analysis 77 USH patients - - Spain - - - - - 1 Global Variome, with Curator vacancy
+?/. - c.1531G>A r.(?) p.(Glu511Lys) - Unknown - likely pathogenic g.216496835C>T - USH2A(NM_206933.4):c.1531G>A (p.E511K) - USH2A_000529 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.1531G>A r.(?) p.(Glu511Lys) - Parent #1 - likely pathogenic g.216496835C>T g.216323493C>T USH2A, variant 1: c.3812-2A>G/p.?, variant 2: c.1531G>A/p.E511K - USH2A_000529 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET9 targeted sequencing panel - see paper retinal disease 1276 PubMed: Weisschuh 2020 Filing key number: 1093, sporadic retinitis pigmentosa, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
+?/. 8 c.1531G>A r.(?) p.(Glu511Lys) - Unknown - likely pathogenic g.216496835C>T - c.1531G>A - USH2A_000529 - PubMed: Colombo-2020 - rs767209934 Germline - - - - - DNA SEQ - - retinal disease - PubMed: Colombo-2020 - F yes - - - - - - 1 LOVD
?/. - c.1531G>A r.(?) p.(Glu511Lys) - Unknown ACMG VUS g.216496835C>T g.216323493C>T - - USH2A_000529 ACMG GN005 criteria: PM2_P PM3_M PP1_P PubMed: Colombo, L. et al., 2022; PubMed: Weisschuh, N. et al., 2020 - rs767209934 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.1531G>A r.(?) p.(Glu511Lys) - Unknown - likely pathogenic g.216496835C>T - USH2A(NM_206933.4):c.1531G>A (p.E511K) - USH2A_000529 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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