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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Owner     
+?/? 40 c.5507T>C r.(?) p.(Leu1836Pro) MyTH4 2 (1747-1896) Paternal (inferred) ACMG VUS g.76916533T>C g.77205488T>C - - MYO7A_000175 Homozygous 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
+?/? 40 c.5507T>C r.(?) p.(Leu1836Pro) MyTH4 2 (1747-1896) Maternal (inferred) ACMG VUS g.76916533T>C g.77205488T>C - - MYO7A_000175 Homozygous 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
+?/+ 40 c.5507T>C r.(?) p.(Leu1836Pro) MyTH4 2 (1747-1896) Parent #2 ACMG VUS g.76916533T>C g.77205488T>C - - MYO7A_000175 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
+?/. - c.5507T>C r.(?) p.(Leu1836Pro) - Parent #2 - likely pathogenic g.76916533T>C g.77205488T>C MYO7A c.5507T>C, p.L1836P - MYO7A_000175 compound heterozygous PubMed: Jauregui 2020 - - Unknown ? - - - - DNA SEQ-NG blood targeted sequencing retinal disease 140 PubMed: Jauregui 2020 - F - (United States) Other - - - - 1 LOVD
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