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.

27 entries on 1 page. Showing entries 1 - 27.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

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Re-site     

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Methylation     

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Disease     

ID_report     

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Owner     
+/. - c.5617C>T r.(?) p.(Arg1873Trp) - Both (homozygous) ACMG pathogenic g.76916643C>T g.77205598C>T - - MYO7A_000032 - PubMed: Trujillano 2017 - - Germline - - - - - DNA SEQ, SEQ-NG - - USH1 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - 1 Daniel Trujillano
+?/? 40 c.5617C>T r.(?) p.(Arg1873Trp) MyTH4 2 (1747-1896) Parent #1 ACMG VUS g.76916643C>T g.77205598C>T - - MYO7A_000032 Heterozygous PubMed: Roux 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs397516321 Germline - 0/1176 controls +BsrDI;-BceAI; - - DNA SEQ - - USH1B ? PubMed: Roux 2006 Proband M - France - - - - - 1 Anne-Françoise Roux
+?/? 40 c.5617C>T r.(?) p.(Arg1873Trp) MyTH4 2 (1747-1896) Paternal (inferred) ACMG VUS g.76916643C>T g.77205598C>T - - MYO7A_000032 Homozygous USMA-USMA missense analysis USMA-missense variant in MSV3d - rs397516321 Germline - - +BsrDI;-BceAI; - - DNA SEQ - - USH1B ? - Proband M - - - - - - - 1 Anne-Françoise Roux
+?/? 40 c.5617C>T r.(?) p.(Arg1873Trp) MyTH4 2 (1747-1896) Maternal (inferred) ACMG VUS g.76916643C>T g.77205598C>T - - MYO7A_000032 Homozygous USMA-USMA missense analysis USMA-missense variant in MSV3d - rs397516321 Germline - - +BsrDI;-BceAI; - - DNA SEQ - - USH1B ? - Proband M - - - - - - - 1 Anne-Françoise Roux
+?/? 40 c.5617C>T r.(?) p.(Arg1873Trp) MyTH4 2 (1747-1896) Paternal (inferred) ACMG VUS g.76916643C>T g.77205598C>T - - MYO7A_000032 Homozygous USMA-USMA missense analysis USMA-missense variant in MSV3d - rs397516321 Germline - - +BsrDI;-BceAI; - - DNA SEQ - - USH1B ? - Proband M - - - - - - - 1 Anne-Françoise Roux
+?/? 40 c.5617C>T r.(?) p.(Arg1873Trp) MyTH4 2 (1747-1896) Maternal (inferred) ACMG VUS g.76916643C>T g.77205598C>T - - MYO7A_000032 Homozygous USMA-USMA missense analysis USMA-missense variant in MSV3d - rs397516321 Germline - - +BsrDI;-BceAI; - - DNA SEQ - - USH1B ? - Proband M - - - - - - - 1 Anne-Françoise Roux
+?/? 40 c.5617C>T r.(?) p.(Arg1873Trp) MyTH4 2 (1747-1896) Unknown ACMG VUS g.76916643C>T g.77205598C>T - - MYO7A_000032 Heterozygous PubMed: Roux 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs397516321 Germline - 0/352 controls +BsrDI;-BceAI; - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband M - - - - - - - 1 Anne-Françoise Roux
+?/? 40 c.5617C>T r.(?) p.(Arg1873Trp) MyTH4 2 (1747-1896) Unknown ACMG VUS g.76916643C>T g.77205598C>T - - MYO7A_000032 Heterozygous PubMed: Roux 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs397516321 Germline - 0/352 controls +BsrDI;-BceAI; - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband F - France - - - - - 1 Anne-Françoise Roux
+?/? 40 c.5617C>T r.(?) p.(Arg1873Trp) MyTH4 2 (1747-1896) Unknown ACMG VUS g.76916643C>T g.77205598C>T - - MYO7A_000032 Heterozygous; Mutation PubMed: Vozzi 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs397516321 Germline - - +BsrDI;-BceAI; - - DNA PE, SEQ - APEX USH1B ? PubMed: Vozzi 2011 Proband - - Italy - - - - - 1 Anne-Françoise Roux
+?/? 40 c.5617C>T r.(?) p.(Arg1873Trp) MyTH4 2 (1747-1896) Parent #2 ACMG VUS g.76916643C>T g.77205598C>T - - MYO7A_000032 Heterozygous PubMed: Sodi 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs397516321 Germline - - +BsrDI;-BceAI; - - DNA SEQ - - USH1B ? PubMed: Sodi 2014 Proband - - Italy - - - - - 1 Anne-Françoise Roux
+?/+ 40 c.5617C>T r.(?) p.(Arg1873Trp) MyTH4 2 (1747-1896) Parent #1 ACMG VUS g.76916643C>T g.77205598C>T - - MYO7A_000032 Heterozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs397516321 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband F - Germany - - - - - 1 Crystel Bonnet
+?/+ 40 c.5617C>T r.(?) p.(Arg1873Trp) MyTH4 2 (1747-1896) Maternal (confirmed) ACMG VUS g.76916643C>T g.77205598C>T - - MYO7A_000032 Homozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs397516321 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband F - France - - - - - 1 Crystel Bonnet
+?/? 40 c.5617C>T r.(?) p.(Arg1873Trp) MyTH4 2 (1747-1896) Paternal (confirmed) ACMG VUS g.76916643C>T g.77205598C>T - - MYO7A_000032 Homozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs397516321 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband F - France - - - - - 1 Crystel Bonnet
+?/+ 40 c.5617C>T r.(?) p.(Arg1873Trp) MyTH4 2 (1747-1896) Parent #1 ACMG VUS g.76916643C>T g.77205598C>T - - MYO7A_000032 Heterozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs397516321 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband M - Italy - - - - - 1 Crystel Bonnet
+?/? 40 c.5617C>T r.(?) p.(Arg1873Trp) MyTH4 2 (1747-1896) Unknown ACMG VUS g.76916643C>T g.77205598C>T - - MYO7A_000032 Heterozygous PubMed: Baux, Vaché 2017; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs397516321 Germline - - +BsrDI;-BceAI; - - DNA SEQ, SEQ-NG-S - - DFNB S1763 PubMed: Baux 2017 Proband F - France - - - - - 1 Anne-Françoise Roux
+?/. - c.5617C>T r.(?) p.(Arg1873Trp) - Parent #1 - likely pathogenic (recessive) g.76916643C>T g.77205598C>T - - MYO7A_000032 - PubMed: Eandi 2017 - - Germline yes - - - - DNA SEQ-NG - 11-gene panel retinal disease Fam13PatTO16 PubMed: Eandi 2017 2-generation family, 2 affected M - Italy - - - - - 2 LOVD
+?/. - c.5617C>T r.(?) p.(Arg1873Trp) - Parent #1 - likely pathogenic (recessive) g.76916643C>T g.77205598C>T - - MYO7A_000032 - PubMed: Eandi 2017 - - Germline yes - - - - DNA SEQ-NG - 11-gene panel retinal disease Fam13PatTO17 PubMed: Eandi 2017 brother M - Italy - - - - - 1 LOVD
+?/. - c.5617C>T r.(?) p.(Arg1873Trp) - Unknown - likely pathogenic g.76916643C>T g.77205598C>T - - MYO7A_000032 - PubMed: Ellingford 2016 - - Germline - - - - - DNA SEQ - 105-gene panel retinal disease 12006582 PubMed: Ellingford 2016 patient - - - - - - - - 1 LOVD
+/. 40 c.5617C>T r.(?) p.(Arg1873Trp) - Parent #1 ACMG pathogenic (recessive) g.76916643C>T - - - MYO7A_000032 - PubMed: Bahena 2021 - - Germline yes - - - - DNA SEQ-NG-I - Exome sequencing USH1B Pat3 PubMed: Bahena 2021 - F no Iran - - - - - 1 Barbara Vona
+/. - c.5617C>T r.(?) p.(Arg1873Trp) - Parent #2 - pathogenic g.76916643C>T g.77205598C>T - - MYO7A_000032 - PubMed: Neuhaus 2017 - - Germline yes - - - - DNA SEQ - - USH Pat87 PubMed: Neuhaus 2017 - - no Italy - - - - - 1 LOVD
+?/. - c.5617C>T r.(?) p.(Arg1873Trp) - Unknown ACMG likely pathogenic g.76916643C>T - - - MYO7A_000032 - PubMed: Mansard et al, 2021 - rs397516321 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - M - - - - - - - 1 Anne-Françoise Roux
+?/. - c.5617C>T r.(?) p.(Arg1873Trp) - Both (homozygous) ACMG likely pathogenic g.76916643C>T - - - MYO7A_000032 - PubMed: Mansard et al, 2021 - rs397516321 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
+?/. - c.5617C>T r.(?) p.(Arg1873Trp) - Paternal (confirmed) ACMG likely pathogenic g.76916643C>T - - - MYO7A_000032 - PubMed: Mansard et al, 2021 - rs397516321 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - M - - - - - - - 1 Anne-Françoise Roux
+?/. - c.5617C>T r.(?) p.(Arg1873Trp) - Parent #1 - likely pathogenic g.76916643C>T g.77205598C>T MYO7A, variant 1: c.5581C>T/p.R1861*, variant 2: c.5617C>T/p.R1873W - MYO7A_000032 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET6 targeted sequencing panel - see paper retinal disease 86 PubMed: Weisschuh 2020 Filing key number: 43, Usher syndrome type I, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
+/. 40 c.5617C>T r.(=) p.(Arg1873Trp) - Maternal (confirmed) - pathogenic (recessive) g.76916643C>T - c.5617C>T - MYO7A_000032 - PubMed: Bakhchane 2017 - - Germline yes 0/100 healthy controls - - - DNA SEQ-NG, SEQ blood - retinal disease SF42.14 PubMed: Bakhchane 2017 - M - - Moroccan - - - - 1 LOVD
+/. 40 c.5617C>T r.(=) p.(Arg1873Trp) - Maternal (confirmed) - pathogenic (recessive) g.76916643C>T - c.5617C>T - MYO7A_000032 - PubMed: Bakhchane 2017 - - Germline yes 0/100 healthy controls - - - DNA SEQ blood - retinal disease SF42:12,13,14,15 PubMed: Bakhchane 2017 - M;F - - Moroccan - - - - 4 LOVD
+/. - c.5617C>T r.(?) p.(Arg1873Trp) - Unknown - pathogenic g.76916643C>T - MYO7A(NM_000260.3):c.5617C>T (p.(Arg1873Trp)) - MYO7A_000032 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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