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.

3 entries on 1 page. Showing entries 1 - 3.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

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DNA change (hg38)     

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+?/? 11 c.1200G>T r.(?) p.(Lys400Asn) Motor domain (1-729) Unknown ACMG VUS g.76871328G>T g.77160282G>T - - MYO7A_000127 Heterozygous PubMed: Roux 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband F - France - - - - - 1 Anne-Françoise Roux
+?/. - c.1200G>T r.(?) p.(Lys400Asn) - Unknown - likely pathogenic g.76871328G>T g.77160282G>T NM_000260, c.1200G>T, p.Lys400Asn - MYO7A_000127 - PubMed: Ezquerra-Inchausti 2018 - - Germline ? - - - - DNA SEQ-NG blood - retinal disease ? PubMed: Ezquerra-Inchausti 2018 Family RP59 ? ? Spain - - - - - 1 LOVD
?/. - c.1200G>T r.(?) p.(Lys400Asn) - Unknown ACMG VUS g.76871328G>T g.77160282G>T MYO7A c.G1200T, p.K400N - MYO7A_000127 marked as causative, heterozygous PubMed: Ma 2021 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ - whole exome sequencing retinal disease 119 PubMed: Ma 2021 - ? - Korea - - - - - 1 LOVD
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