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.

4 entries on 1 page. Showing entries 1 - 4.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

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DNA change (hg38)     

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+?/? 13 c.1370C>T r.(?) p.(Ala457Val) Motor domain (1-729) Parent #1 ACMG VUS g.76873192C>T g.77162146C>T - - MYO7A_000011 Heterozygous PubMed: Ebermann 2007; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033286 Germline - - none - - DNA SEQ - - USH1B ? PubMed: Ebermann 2007 Proband - - Canada - - - - - 1 Anne-Françoise Roux
+?/? 13 c.1370C>T r.(?) p.(Ala457Val) Motor domain (1-729) Unknown ACMG VUS g.76873192C>T g.77162146C>T - - MYO7A_000011 Heterozygous PubMed: Bharadwaj 2000; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033286 Germline - 0/172 controls none - - DNA SEQ - - USH1B ? PubMed: Bharadwaj 2000 Proband - - Ireland - - - - - 1 Anne-Françoise Roux
+?/? 13 c.1370C>T r.(?) p.(Ala457Val) Motor domain (1-729) Parent #1 ACMG VUS g.76873192C>T g.77162146C>T - - MYO7A_000011 Heterozygous; Presumably pathogenic PubMed: Bonnet 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033286 Germline - 0/306 controls none - - DNA SEQ - - USH2 ? PubMed: Bonnet 2011 Proband - - - - - - - - 1 Anne-Françoise Roux
+?/. 13 c.1370C>T r.(?) p.(Ala457Val) - Unknown - likely pathogenic g.76873192C>T - c.1370C>T,p.A457V - MYO7A_000011 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
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