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.

11 entries on 1 page. Showing entries 1 - 11.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

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DNA change (hg38)     

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ClinVar ID     

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Owner     
+?/? 41 c.5648G>A r.(?) p.(Arg1883Gln) MyTH4 2 (1747-1896) Unknown ACMG VUS g.76917153G>A g.77206108G>A - - MYO7A_000233 Heterozygous; UV4 PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033215 Germline - 0/878 controls -BssKI;-StyD4I;-MspI;-HpaII;-ScrFI;-NciI; - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+?/? 41 c.5648G>A r.(?) p.(Arg1883Gln) MyTH4 2 (1747-1896) Unknown ACMG VUS g.76917153G>A g.77206108G>A - - MYO7A_000233 Heterozygous PubMed: Ouyang 2005; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033215 Germline - - -BssKI;-StyD4I;-MspI;-HpaII;-ScrFI;-NciI; - - DNA SEQ - - USH1B ? PubMed: Ouyang 2005 Proband - - United States - - - - - 1 Anne-Françoise Roux
+?/? 41 c.5648G>A r.(?) p.(Arg1883Gln) MyTH4 2 (1747-1896) Maternal (inferred) ACMG VUS g.76917153G>A g.77206108G>A - - MYO7A_000233 Heterozygous; probable pathogenic PubMed: Nakanishi 2010; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033215 Germline - 0/200 controls -BssKI;-StyD4I;-MspI;-HpaII;-ScrFI;-NciI; - - DNA SEQ - - USH1B ? PubMed: Nakanishi 2010 Proband F - Japan - - - - - 1 Anne-Françoise Roux
+?/? 41 c.5648G>A r.(?) p.(Arg1883Gln) MyTH4 2 (1747-1896) Parent #2 ACMG VUS g.76917153G>A g.77206108G>A - - MYO7A_000233 Heterozygous; Presumably pathogenic PubMed: Bonnet 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033215 Germline - 0/306 controls -BssKI;-StyD4I;-MspI;-HpaII;-ScrFI;-NciI; - - DNA SEQ - - USH1B ? PubMed: Bonnet 2011 Proband - - - - - - - - 1 Anne-Françoise Roux
+?/+ 41 c.5648G>A r.(?) p.(Arg1883Gln) MyTH4 2 (1747-1896) Parent #2 ACMG VUS g.76917153G>A g.77206108G>A - - MYO7A_000233 Heterozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033215 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband F - Germany - - - - - 1 Crystel Bonnet
+?/. - c.5648G>A r.(?) p.(Arg1883Gln) - Unknown - likely pathogenic g.76917153G>A g.77206108G>A MYO7A(NM_000260.3):c.5648G>A (p.R1883Q) - MYO7A_000233 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.5648G>A r.(?) p.(Arg1883Gln) - Parent #2 - pathogenic (recessive) g.76917153G>A g.77206108G>A - - MYO7A_000233 - PubMed: Fuster-Garcia 2018 - - Germline - - - - - DNA arraySEQ - - retinal disease RP2069 PubMed: Fuster-Garcia 2018 analysis 77 USH patients - - Spain - - - - - 1 Global Variome, with Curator vacancy
+?/. - c.5648G>A r.(?) p.(Arg1883Gln) - Unknown - likely pathogenic g.76917153G>A g.77206108G>A c.93C>A p.(Cys31*), c.5648G>A p.(Arg1883Gln) - MYO7A_000233 - PubMed: Hagag 2020 - - Germline/De novo (untested) ? - - - - DNA ? - - retinal disease Subject 034 PubMed: Hagag 2020 - ? - - - - - - - 1 LOVD
+/. 41 c.5648G>A r.(?) p.(Gly1883Glu) - Both (homozygous) - pathogenic g.76917153G>A - c.5648G>A - MYO7A_000233 - PubMed: Galbis-Martinez-2021 - - Germline - - - - - DNA ? - - retinal disease - PubMed: Galbis-Martinez-2021 - - - - - - - - - 4 LOVD
+/. - c.5648G>A r.(?) p.(Arg1883Gln) - Maternal (confirmed) - pathogenic (recessive) g.76917153G>A - - - MYO7A_000233 - PubMed: Popp 2022 - rs111033215 Germline - - - - - DNA SEQ, SEQ-NG - WES USH FamPatII12/3 PubMed: Lin 2022 2-generation family, affected brother/sister, unaffected heterozygous carrier parents/relatives F;M yes China - - - - - 2 Johan den Dunnen
+/. - c.5648G>A r.(?) p.(Arg1883Gln) - Unknown ACMG pathogenic (recessive) g.76917153G>A g.77206108G>A - - MYO7A_000233 ACMG PP3, PM2, PM5, PP5_STRONG PubMed: Weisschuh 2024 43294 - Germline - - - - - DNA SEQ-NG - WGS ? USHII-348 PubMed: Weisschuh 2024 patient, no family history M - Germany - - - - - 1 Johan den Dunnen
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