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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Effect     

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AscendingDNA change (cDNA)     

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+?/? 11 c.1189G>A r.(?) p.(Ala397Thr) Motor domain (1-729) Maternal (inferred) ACMG VUS g.76871317G>A g.77160271G>A - - MYO7A_000326 Homozygous; likely pathogenic PubMed: Glöcke 2013; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Glöcke 2013 Proband - - - - - - - - 1 Anne-Françoise Roux
+?/? 11 c.1189G>A r.(?) p.(Ala397Thr) Motor domain (1-729) Paternal (inferred) ACMG VUS g.76871317G>A g.77160271G>A - - MYO7A_000326 Homozygous; likely pathogenic PubMed: Glöcke 2013; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Glöcke 2013 Proband - - - - - - - - 1 Anne-Françoise Roux
+?/? 11 c.1189G>A r.(?) p.(Ala397Thr) Motor domain (1-729) Unknown ACMG VUS g.76871317G>A g.77160271G>A - - MYO7A_000326 Heterozygous PubMed: Kimberling 2010; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - -HgaI;-BsaHI;-Hpy99I; - - DNA SEQ - - DFNB ? PubMed: Kimberling 2010 Proband - No ophtalmologic examination - - United States - - - - - 1 Anne-Françoise Roux
+?/. - c.1189G>A r.(?) p.(Ala397Thr) - Unknown - likely pathogenic g.76871317G>A g.77160271G>A - - MYO7A_000326 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.1189G>A r.(?) p.(Ala397Thr) - Parent #1 - pathogenic g.76871317G>A g.77160271G>A - - MYO7A_000326 - PubMed: Neuhaus 2017 - - Germline yes - - - - DNA SEQ-NG - gene panel USH Pat63 PubMed: Neuhaus 2017 - - no Germany - - - - - 1 LOVD
?/. - c.1189G>A r.(?) p.(Ala397Thr) - Unknown ACMG VUS g.76871317G>A - - - MYO7A_000326 - PubMed: Mansard et al, 2021 - rs1297886521 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - M - - - - - - - 1 Anne-Françoise Roux
+?/. - c.1189G>A r.(?) p.(Ala397Thr) - Parent #1 - likely pathogenic g.76871317G>A g.77160271G>A MYO7A, variant 1: c.1189G>A/p.A397T, variant 2: c.1189G>A/p.A397T - MYO7A_000326 solved, homozygous PubMed: Weisschuh 2020 - - Germline yes - - - - DNA SEQ-NG blood RET2 targeted sequencing panel - see paper retinal disease 123 PubMed: Weisschuh 2020 Filing key number: 55, Usher syndrome type I, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
+?/. 11 c.1189G>A r.(?) p.(Ala397Thr) - Parent #1 - likely pathogenic g.76871317G>A - c.1189G>A,p.A397T - MYO7A_000326 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease 2002(F-LMG353) PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
+?/. 11 c.1189G>A r.(?) p.(Ala397Thr) - Parent #2 - likely pathogenic g.76871317G>A - c.1189G>A,p.A397T - MYO7A_000326 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease 2000(F-LMG353) PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
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