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.

15 entries on 1 page. Showing entries 1 - 15.
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+/+ 7 c.721C>G r.(?) p.(Arg241Gly) Motor domain (1-729) Parent #1 - pathogenic g.76868036C>G g.77156990C>G - - MYO7A_000170 Heterozygous PubMed: Jaijo 2007; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/100 controls - - - DNA SEQ - - USH1B ? PubMed: Jaijo 2007 Proband F - Italy - - - - - 1 Jose Maria Millan
+/+ 7 c.721C>G r.(?) p.(Arg241Gly) Motor domain (1-729) Parent #1 - pathogenic g.76868036C>G g.77156990C>G - - MYO7A_000170 Heterozygous PubMed: Jaijo 2007; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/100 controls - - - DNA minigene, SEQ - - USH1B ? PubMed: Jaijo 2007 Proband - Minigene studies in Aparisi et al., 2013 - - Italy - - - - - 1 Jose Maria Millan
+/+ 7 c.721C>G r.(?) p.(Arg241Gly) Motor domain (1-729) Paternal (inferred) - pathogenic g.76868036C>G g.77156990C>G - - MYO7A_000170 Homozygous PubMed: Jaijo 2007; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/100 controls - - - DNA SEQ - - USH1B ? PubMed: Jaijo 2007 Proband M - Italy - - - - - 1 Jose Maria Millan
+/+ 7 c.721C>G r.(?) p.(Arg241Gly) Motor domain (1-729) Maternal (inferred) - pathogenic g.76868036C>G g.77156990C>G - - MYO7A_000170 Homozygous PubMed: Jaijo 2007; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/100 controls - - - DNA SEQ - - USH1B ? PubMed: Jaijo 2007 Proband M - Italy - - - - - 1 Jose Maria Millan
+/+ 7 c.721C>G r.(?) p.(Arg241Gly) Motor domain (1-729) Paternal (inferred) - pathogenic g.76868036C>G g.77156990C>G - - MYO7A_000170 Heterozygous PubMed: Sodi 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ - - USH1B ? PubMed: Sodi 2014 Proband - - Italy - - - - - 1 Anne-Françoise Roux
+/+ 7 c.721C>G r.(?) p.(Arg241Gly) Motor domain (1-729) Maternal (inferred) - pathogenic g.76868036C>G g.77156990C>G - - MYO7A_000170 Heterozygous PubMed: Sodi 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ - - USH1B ? PubMed: Sodi 2014 Proband - - Italy - - - - - 1 Anne-Françoise Roux
+/+ 7 c.721C>G r.(?) p.(Arg241Gly) Motor domain (1-729) Parent #1 - pathogenic g.76868036C>G g.77156990C>G - - MYO7A_000170 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 - Italy - - - - - 1 Crystel Bonnet
+/+ 7 c.721C>G r.(?) p.(Arg241Gly) Motor domain (1-729) Paternal (inferred) - pathogenic g.76868036C>G g.77156990C>G - - MYO7A_000170 Homozygous; 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 - Italy - - - - - 1 Crystel Bonnet
+/+ 7 c.721C>G r.(?) p.(Arg241Gly) Motor domain (1-729) Maternal (inferred) - pathogenic g.76868036C>G g.77156990C>G - - MYO7A_000170 Homozygous; 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 - Italy - - - - - 1 Crystel Bonnet
+/+ 7 c.721C>G r.(?) p.(Arg241Gly) Motor domain (1-729) Paternal (inferred) - pathogenic g.76868036C>G g.77156990C>G - - MYO7A_000170 Homozygous; 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 - Italy - - - - - 1 Crystel Bonnet
+/+ 7 c.721C>G r.(?) p.(Arg241Gly) Motor domain (1-729) Maternal (inferred) - pathogenic g.76868036C>G g.77156990C>G - - MYO7A_000170 Homozygous; 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 - Italy - - - - - 1 Crystel Bonnet
+/+ 7 c.721C>G r.(?) p.(Arg241Gly) Motor domain (1-729) Paternal (inferred) - pathogenic g.76868036C>G g.77156990C>G - - MYO7A_000170 Homozygous; 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 - Italy - - - - - 1 Crystel Bonnet
+/+ 7 c.721C>G r.(?) p.(Arg241Gly) Motor domain (1-729) Maternal (inferred) - pathogenic g.76868036C>G g.77156990C>G - - MYO7A_000170 Homozygous; 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 - Italy - - - - - 1 Crystel Bonnet
+/+ 7 c.721C>G r.(?) p.(Arg241Gly) Motor domain (1-729) Parent #1 - pathogenic g.76868036C>G g.77156990C>G - - MYO7A_000170 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 - Italy - - - - - 1 Crystel Bonnet
+?/. 7 c.721C>G r.(?) p.(Arg241Gly) - Unknown - likely pathogenic g.76868036C>G - c.721C>G - MYO7A_000170 - PubMed: Colombo-2020 - - Germline - - - - - DNA SEQ - - retinal disease - PubMed: Colombo-2020 - M no - - - - - - 1 LOVD
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