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.

15 entries on 1 page. Showing entries 1 - 15.
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Effect     

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AscendingDNA change (cDNA)     

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+/? 6 c.487G>A r.(?) p.(Gly163Arg) Motor domain (1-729);ATP binding site (158-165) Paternal (inferred) ACMG likely pathogenic g.76867722G>A g.77156676G>A - - MYO7A_000099 Homozygous PubMed: Roux 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/664 controls +BstNI;+PspGI;-HpaII;-NciI;-MspI; - - DNA SEQ - - USH1B ? PubMed: Roux 2006 Proband M - Turkey - - - - - 1 Anne-Françoise Roux
+/? 6 c.487G>A r.(?) p.(Gly163Arg) Motor domain (1-729);ATP binding site (158-165) Maternal (inferred) ACMG likely pathogenic g.76867722G>A g.77156676G>A - - MYO7A_000099 Homozygous PubMed: Roux 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/664 controls +BstNI;+PspGI;-HpaII;-NciI;-MspI; - - DNA SEQ - - USH1B ? PubMed: Roux 2006 Proband M - Turkey - - - - - 1 Anne-Françoise Roux
+/? 6 c.487G>A r.(?) p.(Gly163Arg) Motor domain (1-729);ATP binding site (158-165) Paternal (confirmed) ACMG likely pathogenic g.76867722G>A g.77156676G>A - - MYO7A_000099 Heterozygous PubMed: Roux 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - +BstNI;+PspGI;-HpaII;-NciI;-MspI; - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband F - France - - - - - 1 Anne-Françoise Roux
+/? 6 c.487G>A r.(?) p.(Gly163Arg) Motor domain (1-729), ATP binding site (158-165) Parent #1 ACMG likely pathogenic g.76867722G>A g.77156676G>A - - MYO7A_000099 Heterozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+/? 6 c.487G>A r.(?) p.(Gly163Arg) Motor domain (1-729);ATP binding site (158-165) Paternal (confirmed) ACMG likely pathogenic g.76867722G>A g.77156676G>A - - MYO7A_000099 Heterozygous PubMed: Abdi 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/664 controls +BstNI;+PspGI;-HpaII;-NciI;-MspI; - - DNA SEQ - - USH1B ? PubMed: Abdi 2016 Proband M - Algeria - - - - - 1 Crystel Bonnet
+/. 6 c.487G>A r.(?) p.(Gly163Arg) - Both (homozygous) ACMG pathogenic (recessive) g.76867722G>A - - - MYO7A_000099 - PubMed: Bahena 2021 - - Germline yes - - - - DNA SEQ-NG-I - Exome sequencing USH1B Pat8 PubMed: Bahena 2021 - F yes Iran - - - - - 1 Barbara Vona
+/. 6 c.487G>A r.(?) p.(Gly163Arg) - Parent #2 ACMG pathogenic (recessive) g.76867722G>A - - - MYO7A_000099 - - - - Germline yes - - - - DNA SEQ-NG-I - Exome sequencing USH Pat13 PubMed: Bahena 2021 - M no Mexico - - - - - 2 Barbara Vona
+?/. - c.487G>A r.(?) p.(Gly163Arg) - Both (homozygous) ACMG likely pathogenic (recessive) g.76867722G>A g.77156676G>A NM_000260.3:c.487G>A;p.(Gly163Arg) - MYO7A_000099 - PubMed: Patel 2018 - rs28937873 Germline yes - - - - DNA SEQ-NG - 322 eye disease gene panel retinal disease 15DG0530 PubMed: Patel 2018 - - yes Saudi Arabia - - - - - 1 LOVD
+?/. - c.487G>A r.(?) p.(Gly163Arg) - Maternal (confirmed) ACMG likely pathogenic g.76867722G>A - - - MYO7A_000099 - PubMed: Mansard et al, 2021 - rs1472566324 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - ? - - - - - - - 1 Anne-Françoise Roux
+?/. - c.487G>A r.(?) p.(Gly163Arg) - Both (homozygous) ACMG likely pathogenic g.76867722G>A - - - MYO7A_000099 - PubMed: Mansard et al, 2021 - rs1472566324 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
+?/. 6 c.487G>A r.(?) p.(Gly163Arg) - Parent #1 - likely pathogenic g.76867722G>A - c.487G>A,p.G163R - MYO7A_000099 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease 2000(F-LMG353) PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
+?/. 6 c.487G>A r.(?) p.(Gly163Arg) - Parent #1 - likely pathogenic g.76867722G>A - c.487G>A,p.G163R - MYO7A_000099 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease 2001(F-LMG353) PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
+?/. 6 c.487G>A r.(?) p.(Gly163Arg) - Paternal (confirmed) - likely pathogenic (recessive) g.76867722G>A - c.487G>A - MYO7A_000099 - PubMed: Khateb 2020 - - Germline yes - - - - DNA ? - - retinal disease CIC00417 PubMed: Khateb 2020 Two affected brothers M - - - - - - - 1 LOVD
+?/. 6 c.487G>A r.(?) p.(Gly163Arg) - Paternal (confirmed) - likely pathogenic (recessive) g.76867722G>A - c.487G>A p.Gly163Arg - MYO7A_000099 - PubMed: Khateb 2020 - - Germline yes - - - - DNA ? - - retinal disease CIC00418 PubMed: Khateb 2020 Two affected brothers M - - - - - - - 1 LOVD
+?/. 6 c.487G>A r.(?) p.(Gly163Arg) - Parent #1 - likely pathogenic (recessive) g.76867722G>A - c.487G>A p.Gly163Arg - MYO7A_000099 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease CIC01199 PubMed: Khateb 2020 Two affected brothers M - - - - - - - 1 LOVD
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