Full data view for gene MYO7A


This database is one of the ”Retinal and hearing impairment genetic variant databases”.
Information The variants shown are described using the NM_000260.3 transcript reference sequence.

10 entries on 1 page. Showing entries 1 - 10.
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+?/? 27 c.3503G>A r.(?) p.(Arg1168Gln) MyTH4 1 (1017-1253) Parent #2 ACMG VUS g.76895760G>A g.77184715G>A - - MYO7A_000521 Heterozygous; UV3 PubMed: Aparisi 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 ? PubMed: Aparisi 2014 Proband - - Spain - - - - - 1 Anne-Françoise Roux
+?/? 27 c.3503G>A r.(?) p.(Arg1168Gln) MyTH4 1 (1017-1253) Parent #2 ACMG VUS g.76895760G>A g.77184715G>A - - MYO7A_000521 Heterozygous; UV3 PubMed: Aparisi 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Aparisi 2014 Proband - - Spain - - - - - 1 Anne-Françoise Roux
+?/+ 27 c.3503G>A r.(?) p.(Arg1168Gln) MyTH4 1 (1017-1253) Parent #1 ACMG VUS g.76895760G>A g.77184715G>A - - MYO7A_000521 Heterozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S, PCRq - - USH1B ? PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+/. - c.3503G>A r.(?) p.(Arg1168Gln) - Both (homozygous) - pathogenic (recessive) g.76895760G>A g.77184715G>A - - MYO7A_000521 - PubMed: Fuster-Garcia 2018 - - Germline - - - - - DNA arraySEQ - - retinal disease RP1944 PubMed: Fuster-Garcia 2018 analysis 77 USH patients - - Spain - - - - - 1 Global Variome, with Curator vacancy
+/. 27A c.3503G>A r.(?) p.(Arg1168Gln) - Parent #1 - pathogenic (recessive) g.76895760G>A g.77184715G>A - - MYO7A_000521 - PubMed: Dad 2016 - - Germline - - - - - DNA SEQ-NG - gene panel USH retinal disease USH1-3 PubMed: Dad 2016 - F no Denmark - - - - - 1 LOVD
+?/. - c.3503G>A r.(?) p.(Arg1168Gln) - Parent #1 - likely pathogenic g.76895760G>A g.77184715G>A - - MYO7A_000521 - PubMed: Neuhaus 2017 - - Germline - - - - - DNA SEQ-NG - gene panel USH Pat13 PubMed: Neuhaus 2017 - - no Germany - - - - - 1 LOVD
+/. - c.3503G>A r.(?) p.(Arg1168Gln) - Parent #1 - pathogenic g.76895760G>A g.77184715G>A - - MYO7A_000521 - PubMed: Neuhaus 2017 - - Germline - - - - - DNA SEQ-NG - gene panel USH Pat14 PubMed: Neuhaus 2017 - - no Germany - - - - - 1 LOVD
+?/. - c.3503G>A r.(?) p.(Arg1168Gln) - Paternal (confirmed) ACMG likely pathogenic g.76895760G>A - - - MYO7A_000521 - PubMed: Mansard et al, 2021 - rs797044516 Germline - - - - - DNA SEQ-NG, SEQ - - USH2A - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
+?/. - c.3503G>A r.(?) p.(Arg1168Gln) - Parent #1 - likely pathogenic g.76895760G>A g.77184715G>A MYO7A, variant 1: c.1996C>T/p.R666*, variant 2: c.3503G>A/p.R1168Q - MYO7A_000521 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET8 targeted sequencing panel - see paper retinal disease 126 PubMed: Weisschuh 2020 Filing key number: 56, Usher syndrome type I, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
+?/. 27 c.3503G>A r.(?) p.(Arg1168Gln) - Parent #1 - likely pathogenic (recessive) g.76895760G>A - c.3503G>A p.Arg1168Gln - MYO7A_000521 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease CIC06471 PubMed: Khateb 2020 one affected brother F - - French - - - - 1 LOVD
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