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.

7 entries on 1 page. Showing entries 1 - 7.
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Effect     

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AscendingDNA change (cDNA)     

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+?/? 5 c.397C>T r.(?) p.(His133Tyr) Motor domain (1-729) Parent #1 ACMG VUS g.76867064C>T g.77156018C>T - - MYO7A_000272 Heterozygous PubMed: Roux 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033403 Germline - - - - - DNA minigene, SEQ - - USH1B ? PubMed: Roux 2011 Proband M - France - - - - - 1 Anne-Françoise Roux
+?/? 5 c.397C>T r.(?) p.(His133Tyr) Motor domain (1-729) Parent #1 ACMG VUS g.76867064C>T g.77156018C>T - - MYO7A_000272 Heterozygous PubMed: Le Guédard-Méreuze 2010; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033403 Germline - - - - - DNA minigene, SEQ - - USH1B ? PubMed: Le Guédard-Méreuze 2010 Relative M - France - - - - - 1 Anne-Françoise Roux
+/. - c.397C>T r.(?) p.(His133Tyr) - Parent #1 - pathogenic g.76867064C>T g.77156018C>T - - MYO7A_000272 - PubMed: Neuhaus 2017 - rs111033403 Germline - - - - - DNA SEQ-NG - gene panel USH Pat101 PubMed: Neuhaus 2017 - - no Saudi Arabia - - - - - 1 LOVD
+?/. - c.397C>T r.(?) p.(His133Tyr) - Both (homozygous) ACMG likely pathogenic g.76867064C>T g.77156018C>T MYO7A c.397C>T, p.(His133Tyr) - MYO7A_000272 homozygous PubMed: Dineiro 2020 - - Germline ? - - - - DNA SEQ-NG-I, SEQ blood, saliva targeted sequencing with 1 of 4 panels of OFTALMOgenics probes retinal disease OFTALMO.018 PubMed: Dineiro 2020 - ? - Spain - - - - - 1 LOVD
+/. 5 c.397C>T r.(?) p.(His133Tyr) - Both (homozygous) - pathogenic g.76867064C>T - c.397C>T - MYO7A_000272 - PubMed: Galbis-Martinez-2021 - - Germline - - - - - DNA ? - - retinal disease - PubMed: Galbis-Martinez-2021 - - - - - - - - - 8 LOVD
+/. 5 c.397C>T r.(?) p.(His133Tyr) - Both (homozygous) - pathogenic g.76867064C>T - c.397C>T - MYO7A_000272 - PubMed: Galbis-Martinez-2021 - - Germline - - - - - DNA ? - - retinal disease - PubMed: Galbis-Martinez-2021 - - - - - - - - - 4 LOVD
+/. 5 c.397C>T r.(?) p.(His133Tyr) - Both (homozygous) - pathogenic g.76867064C>T - c.397C>T - MYO7A_000272 - PubMed: Galbis-Martinez-2021 - - Germline - - - - - DNA ? - - retinal disease - PubMed: Galbis-Martinez-2021 - - - - - - - - - 4 LOVD
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