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.

17 entries on 1 page. Showing entries 1 - 17.
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Effect     

Exon     

AscendingDNA change (cDNA)     

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+?/. - c.5573T>C r.(?) p.(Leu1858Pro) - Unknown - likely pathogenic g.76916599T>C g.77205554T>C MYO7A(NM_000260.3):c.5573T>C (p.L1858P), MYO7A(NM_000260.4):c.5573T>C (p.L1858P) - MYO7A_000080 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/+ 40 c.5573T>C r.(?) p.(Leu1858Pro) MyTH4 2 (1747-1896) Unknown ACMG likely pathogenic g.76916599T>C g.77205554T>C - - MYO7A_000080 Heterozygous PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/878 controls +FauI;+AciI;-PstI;-HpyCH4V;-SfcI; - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/? 40 c.5573T>C r.(?) p.(Leu1858Pro) MyTH4 2 (1747-1896) Parent #2 ACMG likely pathogenic g.76916599T>C g.77205554T>C - - MYO7A_000080 Heterozygous PubMed: Roux 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/1176 controls +FauI;+AciI;-PstI;-HpyCH4V;-SfcI; - - DNA SEQ - - USH1B ? PubMed: Roux 2006 Proband F - France - - - - - 1 Anne-Françoise Roux
+/? 40 c.5573T>C r.(?) p.(Leu1858Pro) MyTH4 2 (1747-1896) Parent #1 ACMG likely pathogenic g.76916599T>C g.77205554T>C - - MYO7A_000080 Heterozygous PubMed: Blanchet 2007; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - +FauI;+AciI;-PstI;-HpyCH4V;-SfcI; - - DNA SEQ - - USH1B ? PubMed: Blanchet 2007 Proband M - France - - - - - 1 Anne-Françoise Roux
+/? 40 c.5573T>C r.(?) p.(Leu1858Pro) MyTH4 2 (1747-1896) Parent #2 ACMG likely pathogenic g.76916599T>C g.77205554T>C - - MYO7A_000080 Heterozygous PubMed: Roux 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - +FauI;+AciI;-PstI;-HpyCH4V;-SfcI; - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband F - France - - - - - 1 Anne-Françoise Roux
+/? 40 c.5573T>C r.(?) p.(Leu1858Pro) MyTH4 2 (1747-1896) Unknown ACMG likely pathogenic g.76916599T>C g.77205554T>C - - MYO7A_000080 Heterozygous PubMed: Bharadwaj 2000; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/172 controls +FauI;+AciI;-PstI;-HpyCH4V;-SfcI; - - DNA SEQ - - USH1B ? PubMed: Bharadwaj 2000 Proband - - Canada - - - - - 1 Anne-Françoise Roux
+/? 40 c.5573T>C r.(?) p.(Leu1858Pro) MyTH4 2 (1747-1896) Parent #1 ACMG likely pathogenic g.76916599T>C g.77205554T>C - - MYO7A_000080 Heterozygous PubMed: Jacobson 2008; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - +FauI;+AciI;-PstI;-HpyCH4V;-SfcI; - - DNA SEQ - - USH1B ? PubMed: Jacobson 2008 Proband F - - - - - - - 1 Anne-Françoise Roux
+/? 40 c.5573T>C r.(?) p.(Leu1858Pro) MyTH4 2 (1747-1896) Parent #2 ACMG likely pathogenic g.76916599T>C g.77205554T>C - - MYO7A_000080 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 F - Germany - - - - - 1 Crystel Bonnet
+/? 40 c.5573T>C r.(?) p.(Leu1858Pro) MyTH4 2 (1747-1896) Parent #1 ACMG likely pathogenic g.76916599T>C g.77205554T>C - - MYO7A_000080 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 M - Spain - - - - - 1 Crystel Bonnet
+?/. - c.5573T>C r.(?) p.(Leu1858Pro) - Unknown - likely pathogenic g.76916599T>C g.77205554T>C MYO7A(NM_000260.3):c.5573T>C (p.L1858P), MYO7A(NM_000260.4):c.5573T>C (p.L1858P) - MYO7A_000080 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.5573T>C r.(?) p.(Leu1858Pro) - Unknown - likely pathogenic g.76916599T>C g.77205554T>C MYO7A(NM_000260.3):c.5573T>C (p.L1858P), MYO7A(NM_000260.4):c.5573T>C (p.L1858P) - MYO7A_000080 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. 40 c.5573T>C r.(?) p.(Leu1858Pro) - Both (homozygous) ACMG pathogenic (recessive) g.76916599T>C - - - MYO7A_000080 - Bahena et al., 2021 - - Germline yes - - - - DNA SEQ-NG-I - Exome sequencing USH1B Pat4 PubMed: Bahena 2021 - F yes Iran - - - - - 3 Barbara Vona
+/. - c.5573T>C r.(?) p.(Leu1858Pro) - Parent #2 - pathogenic g.76916599T>C g.77205554T>C - - MYO7A_000080 - PubMed: Neuhaus 2017 - - Germline - - - - - DNA SEQ-NG - gene panel USH Pat14 PubMed: Neuhaus 2017 - - no Germany - - - - - 1 LOVD
+?/. - c.5573T>C r.(?) p.(Leu1858Pro) - Paternal (confirmed) ACMG likely pathogenic g.76916599T>C - - - MYO7A_000080 - PubMed: Mansard et al, 2021 - rs368657015 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
+?/. 40 c.5573T>C r.(?) p.(Leu1858Pro) - Parent #2 - likely pathogenic (recessive) g.76916599T>C - c.5573T>C p.Leu1858Pro - MYO7A_000080 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease 1027955 PubMed: Khateb 2020 simplex case F - - French - - - - 1 LOVD
+?/. 40 c.5573T>C r.(?) p.(Leu1858Pro) - Parent #2 - likely pathogenic (recessive) g.76916599T>C - c.5573T>C p.Leu1858Pro - MYO7A_000080 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease CIC08509 PubMed: Khateb 2020 Simplex case F - - - - - - - 1 LOVD
+/. - c.5573T>C r.(?) p.(Leu1858Pro) - Unknown ACMG pathogenic (recessive) g.76916599T>C g.77205554T>C - - MYO7A_000080 ACMG PP3, PM2, PP5_STRONG PubMed: Weisschuh 2024 43288 - Germline - - - - - DNA SEQ-NG - WGS ? USHI-73 PubMed: Weisschuh 2024 patient, no family history F - Germany - - - - - 1 Johan den Dunnen
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