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.

10 entries on 1 page. Showing entries 1 - 10.
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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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Reference     

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Owner     
+?/? 7 c.722G>A r.(?) p.(Arg241His) Motor domain (1-729) Parent #2 ACMG VUS g.76868037G>A g.77156991G>A - - MYO7A_000284 Heterozygous PubMed: Roux 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033284 Germline - 0/180 controls +NspI;+FatI;+NlaIII;-HpyCH4IV;-PmlI;-BsaAI; - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband F - France - - - - - 1 Anne-Françoise Roux
+?/+ 7 c.722G>A r.(?) p.(Arg241His) Motor domain (1-729) Parent #2 ACMG VUS g.76868037G>A g.77156991G>A - - MYO7A_000284 Heterozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033286 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+?/+ 7 c.722G>A r.(?) p.(Arg241His) Motor domain (1-729) Parent #1 ACMG VUS g.76868037G>A g.77156991G>A - - MYO7A_000284 Heterozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033286 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband M - Spain - - - - - 1 Crystel Bonnet
+?/. 7 c.722G>A r.(?) p.(Arg241His) - Parent #1 ACMG likely pathogenic (recessive) g.76868037G>A - - - MYO7A_000284 - - - - Germline yes - - - - DNA SEQ-NG-I - Exome sequencing USH Pat11 PubMed: Bahena 2021 - F no Mexico - - - - - 5 Barbara Vona
+?/. - c.722G>A r.(?) p.(Arg241His) - Unknown - likely pathogenic g.76868037G>A - - - MYO7A_000284 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. 7 c.722G>A r.(?) p.(Arg241His) - Parent #2 - likely pathogenic (recessive) g.76868037G>A - c.722G>A p.Arg241His - MYO7A_000284 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease CIC08846 PubMed: Khateb 2020 one affected sister M - - French - - - - 1 LOVD
+?/. 7 c.722G>A r.(?) p.(Arg241His) - Parent #2 - likely pathogenic (recessive) g.76868037G>A - c.722G>A - MYO7A_000284 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease CIC06731 PubMed: Khateb 2020 one affected brother F - - French - - - - 1 LOVD
+/. - c.722G>A r.(?) p.(Arg241His) - Both (homozygous) - pathogenic (recessive) g.76868037G>A g.77156991G>A - - MYO7A_000284 - PubMed: Richard 2019 - - Germline - - - - - DNA SEQ, SEQ-NG - - HL DEM4141 PubMed: Richard 2019 - - yes Pakistan - - - - - 1 Johan den Dunnen
+/. - c.722G>A r.(?) p.(Arg241His) - Both (homozygous) - pathogenic (recessive) g.76868037G>A g.77156991G>A - - MYO7A_000284 - PubMed: Richard 2019 - - Germline - - - - - DNA SEQ, SEQ-NG - - HL DEM4299 PubMed: Richard 2019 - - yes Pakistan - - - - - 1 Johan den Dunnen
+/. - c.722G>A r.(?) p.(Arg241His) - Both (homozygous) - pathogenic (recessive) g.76868037G>A g.77156991G>A - - MYO7A_000284 - PubMed: Richard 2019 - - Germline - - - - - DNA SEQ, SEQ-NG - - HL DEM4365 PubMed: Richard 2019 - - yes Pakistan - - - - - 1 Johan den Dunnen
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