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)     

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+?/? 14 c.1556G>A r.(?) p.(Gly519Asp) Motor domain (1-729) Maternal (confirmed) ACMG VUS g.76873900G>A g.77162854G>A - - MYO7A_000017 Heterozygous PubMed: Bonnet 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033206 Germline - 0/306 controls -BaeGI;-Bsp1286I; - - DNA SEQ - - USH1 - PubMed: Bonnet 2011 Proband F - - - - - - - 1 Anne-Françoise Roux
+?/? 14 c.1556G>A r.(?) p.(Gly519Asp) Motor domain (1-729) Parent #1 ACMG VUS g.76873900G>A g.77162854G>A - - MYO7A_000017 Heterozygous PubMed: Roux 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033206 Germline - 0/352 controls -BaeGI;-Bsp1286I; - - DNA SEQ - - USH1B ? PubMed: Roux 2006 Proband M - France - - - - - 1 Anne-Françoise Roux
+?/? 14 c.1556G>A r.(?) p.(Gly519Asp) Motor domain (1-729) Paternal (inferred) ACMG VUS g.76873900G>A g.77162854G>A - - MYO7A_000017 Homozygous PubMed: Bharadwaj 2000; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033206 Germline - 0/172 controls -BaeGI;-Bsp1286I; - - DNA SEQ - - USH1B ? PubMed: Bharadwaj 2000 Proband - - Ireland - - - - - 1 Anne-Françoise Roux
+?/? 14 c.1556G>A r.(?) p.(Gly519Asp) Motor domain (1-729) Maternal (inferred) ACMG VUS g.76873900G>A g.77162854G>A - - MYO7A_000017 Homozygous PubMed: Bharadwaj 2000; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033206 Germline - 0/172 controls -BaeGI;-Bsp1286I; - - DNA SEQ - - USH1B ? PubMed: Bharadwaj 2000 Proband - - Ireland - - - - - 1 Anne-Françoise Roux
+?/? 14 c.1556G>A r.(?) p.(Gly519Asp) Motor domain (1-729) Unknown ACMG VUS g.76873900G>A g.77162854G>A - - MYO7A_000017 Heterozygous PubMed: Bujakowska 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033206 Germline - - -BaeGI;-Bsp1286I; - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bujakowska 2014 Proband - - United States - - - - - 1 Anne-Françoise Roux
+?/. - c.1556G>A r.(?) p.(Gly519Asp) - Paternal (confirmed) ACMG likely pathogenic g.76873900G>A - - - MYO7A_000017 - PubMed: Mansard et al, 2021 - rs111033206 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - M - - - - - - - 1 Anne-Françoise Roux
+?/. - c.1556G>A r.(?) p.(Gly519Asp) - Unknown ACMG likely pathogenic g.76873900G>A - - - MYO7A_000017 - PubMed: Mansard et al, 2021 - rs111033206 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - M - - - - - - - 1 Anne-Françoise Roux
+?/. 14 c.1556G>A r.(?) p.(Gly519Asp) - Unknown - likely pathogenic g.76873900G>A - p.G519D - MYO7A_000017 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
+?/. 14 c.1556G>A r.(?) p.(Gly519Asp) - Parent #1 - likely pathogenic (recessive) g.76873900G>A - c.1556G>A - MYO7A_000017 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease 1744338 PubMed: Khateb 2020 One affected sister M - - - - - - - 1 LOVD
+?/. 14 c.1556G>A r.(?) p.(Gly519Asp) - Parent #1 - likely pathogenic (recessive) g.76873900G>A - c.1556G>A - MYO7A_000017 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease 1744335 PubMed: Khateb 2020 One affected brother F - - - - - - - 1 LOVD
+?/. 14 c.1556G>A r.(?) p.(Gly519Asp) - Parent #1 - likely pathogenic (recessive) g.76873900G>A - c.1556G>A - MYO7A_000017 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease CIC06286 PubMed: Khateb 2020 simplex case F - - French - - - - 1 LOVD
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