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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-/- 35 c.4697C>T r.(?) p.(Thr1566Met) FERM 1 (1258-1602) Unknown - benign g.76910708C>T g.77199663C>T - - MYO7A_000082 Heterozygous PubMed: Licastro 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs41298747 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Licastro 2012 Proband - - Italy - - - - - 1 Anne-Françoise Roux
-/- 35 c.4697C>T r.(?) p.(Thr1566Met) FERM 1 (1258-1602) Parent #1 - benign g.76910708C>T g.77199663C>T - - MYO7A_000082 Heterozygous PubMed: Roux 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs41298747 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Roux 2006 Proband F - France - - - - - 1 Anne-Françoise Roux
-/- 35 c.4697C>T r.(?) p.(Thr1566Met) FERM 1 (1258-1602) Unknown - benign g.76910708C>T g.77199663C>T - - MYO7A_000082 Heterozygous PubMed: Najera 2002; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs41298747 Germline - 0/200 controls - - - DNA SEQ - - USH1B ? PubMed: Najera 2002 Proband - - Spain - - - - - 1 Jose Maria Millan
-/- 35 c.4697C>T r.(?) p.(Thr1566Met) FERM 1 (1258-1602) Paternal (inferred) - benign g.76910708C>T g.77199663C>T - - MYO7A_000082 Homozygous PubMed: Le Guédard-Méreuze 2010; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs41298747 Germline - - - - - DNA minigene, SEQ - - USH1B ? PubMed: Le Guédard-Méreuze 2010 Proband F - Algeria - - - - - 1 Anne-Françoise Roux
-/- 35 c.4697C>T r.(?) p.(Thr1566Met) FERM 1 (1258-1602) Maternal (inferred) - benign g.76910708C>T g.77199663C>T - - MYO7A_000082 Homozygous PubMed: Le Guédard-Méreuze 2010; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs41298747 Germline - - - - - DNA minigene, SEQ - - USH1B ? PubMed: Le Guédard-Méreuze 2010 Proband F - Algeria - - - - - 1 Anne-Françoise Roux
-/- 35 c.4697C>T r.(?) p.(Thr1566Met) FERM 1 (1258-1602) Maternal (confirmed) - benign g.76910708C>T g.77199663C>T - - MYO7A_000082 Heterozygous; potential PubMed: Vastinsalo 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs41298747 Germline - 0/150 controls - - - DNA PE, SEQ - APEX USH2 ? PubMed: Vastinsalo 2012 Proband M - Finland - - - - - 1 Anne-Françoise Roux
-/. - c.4697C>T r.(?) p.(Thr1566Met) - Unknown - benign g.76910708C>T g.77199663C>T MYO7A(NM_000260.3):c.4697C>T (p.T1566M), MYO7A(NM_000260.4):c.4697C>T (p.T1566M) - MYO7A_000082 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.4697C>T r.(?) p.(Thr1566Met) - Unknown - VUS g.76910708C>T g.77199663C>T MYO7A(NM_000260.3):c.4697C>T (p.T1566M), MYO7A(NM_000260.4):c.4697C>T (p.T1566M) - MYO7A_000082 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.4697C>T r.(?) p.(Thr1566Met) - Parent #1 - likely pathogenic g.76910708C>T g.77199663C>T - - MYO7A_000082 - PubMed: Holtan 2020 - - Germline - 1/899 cases - - - DNA SEQ - - retinal disease - PubMed: Holtan 2020 1 patient with variant in heterozygous or compound heterozygous form - - Norway - - - - - 1 Global Variome, with Curator vacancy
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