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 (genomic) (hg19)     

DNA change (hg38)     

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Owner     
+?/? 9 c.977T>A r.(?) p.(Leu326Gln) Motor domain (1-729) Unknown ACMG VUS g.76869450T>A g.77158404T>A - - MYO7A_000248 Heterozygous; UV2 PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/96 controls +PflMI;+AlwNI;-BsgI;-HpyCH4V; - - DNA SEQ - - USH - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+?/? 9 c.977T>A r.(?) p.(Leu326Gln) Motor domain (1-729) Paternal (inferred) ACMG VUS g.76869450T>A g.77158404T>A - - MYO7A_000248 Homozygous PubMed: Riazuddin 2008; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/192 controls - - - DNA SEQ - - USH1B ? PubMed: Riazuddin 2008 Proband - - Pakistan - - - - - 1 Anne-Françoise Roux
+?/? 9 c.977T>A r.(?) p.(Leu326Gln) Motor domain (1-729) Maternal (inferred) ACMG VUS g.76869450T>A g.77158404T>A - - MYO7A_000248 Homozygous PubMed: Riazuddin 2008; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/192 controls - - - DNA SEQ - - USH1B ? PubMed: Riazuddin 2008 Proband - - Pakistan - - - - - 1 Anne-Françoise Roux
+/. - c.977T>A r.(?) p.(Leu326Gln) - Both (homozygous) - pathogenic (recessive) g.76869450T>A g.77158404T>A - - MYO7A_000248 - PubMed: Richard 2019 - - Germline - - - - - DNA SEQ, SEQ-NG - - HL PKDF370 PubMed: Richard 2019 - - yes Pakistan - - - - - 1 Johan den Dunnen
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