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.

9 entries on 1 page. Showing entries 1 - 9.
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AscendingDNA change (cDNA)     

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+?/? 11 c.1097T>C r.(?) p.(Leu366Pro) Motor domain (1-729) Parent #2 ACMG VUS g.76871225T>C g.77160179T>C - - MYO7A_000167 Heterozygous PubMed: Jaijo 2007; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/100 controls - - - DNA minigene, SEQ - - USH1B ? PubMed: Jaijo 2007 Proband - Minigene studies in Aparisi et al., 2013 M - Italy - - - - - 1 Jose Maria Millan
+?/+ 11 c.1097T>C r.(?) p.(Leu366Pro) Motor domain (1-729) Parent #2 ACMG VUS g.76871225T>C g.77160179T>C - - MYO7A_000167 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 - - Slovenia - - - - - 1 Crystel Bonnet
+?/+ 11 c.1097T>C r.(?) p.(Leu366Pro) Motor domain (1-729) Paternal (inferred) ACMG VUS g.76871225T>C g.77160179T>C - - MYO7A_000167 Homozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband - - Slovenia - - - - - 1 Crystel Bonnet
+?/? 11 c.1097T>C r.(?) p.(Leu366Pro) Motor domain (1-729) Maternal (inferred) ACMG VUS g.76871225T>C g.77160179T>C - - MYO7A_000167 Homozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband - - Slovenia - - - - - 1 Crystel Bonnet
+?/+ 11 c.1097T>C r.(?) p.(Leu366Pro) Motor domain (1-729) Paternal (inferred) ACMG VUS g.76871225T>C g.77160179T>C - - MYO7A_000167 Homozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband - - Slovenia - - - - - 1 Crystel Bonnet
+?/? 11 c.1097T>C r.(?) p.(Leu366Pro) Motor domain (1-729) Maternal (inferred) ACMG VUS g.76871225T>C g.77160179T>C - - MYO7A_000167 Homozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband - - Slovenia - - - - - 1 Crystel Bonnet
+?/. 11 c.1097T>C r.(?) p.(Leu366Pro) - Unknown - likely pathogenic g.76871225T>C - c.1097T>C - MYO7A_000167 - PubMed: Colombo-2020 - rs397516281 Germline - - - - - DNA SEQ - - retinal disease - PubMed: Colombo-2020 - M no - - - - - - 1 LOVD
+?/. - c.1097T>C r.(?) p.(Leu366Pro) - Unknown ACMG likely pathogenic (recessive) g.76871225T>C g.77160179T>C - - MYO7A_000167 ACMG PP3, PM2, PP5_STRONG PubMed: Weisschuh 2024 43133 - Germline - - - - - DNA SEQ-NG - WGS ? USHI-84 PubMed: Weisschuh 2024 patient, no family history F - Germany - - - - - 1 Johan den Dunnen
+?/. - c.1097T>C r.(?) p.(Leu366Pro) - Unknown ACMG likely pathogenic (recessive) g.76871225T>C g.77160179T>C - - MYO7A_000167 ACMG PP3, PM2, PP5_STRONG PubMed: Weisschuh 2024 43133 - Germline - - - - - DNA SEQ-NG - WGS ? USHII-348 PubMed: Weisschuh 2024 patient, no family history M - Germany - - - - - 1 Johan den Dunnen
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