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.

6 entries on 1 page. Showing entries 1 - 6.
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Effect     

Exon     

AscendingDNA change (cDNA)     

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DNA change (hg38)     

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+/+ 25 c.3262C>T r.(?) p.(Gln1088*) MyTH4 1 (1017-1253) Maternal (confirmed) - pathogenic g.76893622C>T g.77182577C>T - - MYO7A_000493 Heterozygous; likely pathogenic PubMed: Glöcke 2013 - - Germline - - -AlwNI;-ApeKI;-BbvI;-BstAPI;-Cac8I;-Fnu4HI; - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Glöcke 2013 Proband - - - - - - - - 1 Anne-Françoise Roux
+/+ 25 c.3262C>T r.(?) p.(Gln1088*) MyTH4 1 (1017-1253) Parent #2 - pathogenic g.76893622C>T g.77182577C>T - - MYO7A_000493 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband - - Slovenia - - - - - 1 Crystel Bonnet
+/. 25 c.3262C>T r.(?) p.(Gln1088*) MyTH4 1 (1017-1253) Parent #2 - pathogenic (recessive) g.76893622C>T - - - MYO7A_000493 - PubMed: Ivanova 2018 - - Germline - - -AlwNI;-ApeKI;-BbvI;-BstAPI;-Cac8I;-Fnu4HI; - - DNA SEQ-NG-S - - USH1B Pat23 PubMed: Ivanova 2018 Proband M - Russian Federation Slavonian - - - - 1 Vladimir Strelnikov
+/. 25 c.3262C>T r.(?) p.(Gln1088*) MyTH4 1 (1017-1253) Unknown - likely pathogenic (recessive) g.76893622C>T - - - MYO7A_000493 - PubMed: Ivanova 2018 - - Germline - - -AlwNI;-ApeKI;-BbvI;-BstAPI;-Cac8I;-Fnu4HI; - - DNA SEQ-NG-S - - USH1B Pat22 PubMed: Ivanova 2018 Proband F - Russian Federation Slavonian - - - - 1 Vladimir Strelnikov
+/. - c.3262C>T r.(?) p.(Gln1088*) - Unknown ACMG pathogenic g.76893622C>T - - - MYO7A_000493 - PubMed: Sharon 2019 - - Germline - 1/2420 IRD families - - - DNA SEQ - - retinal disease - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - 1 Global Variome, with Curator vacancy
+?/. - c.3262C>T r.(?) p.(Gln1088*) - Parent #1 - likely pathogenic g.76893622C>T g.77182577C>T - - MYO7A_000493 - PubMed: Neuhaus 2017 - - Germline - - - - - DNA SEQ-NG - gene panel USH Pat11 PubMed: Neuhaus 2017 - - no Germany - - - - - 1 LOVD
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