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.

5 entries on 1 page. Showing entries 1 - 5.
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Effect     

Exon     

AscendingDNA change (cDNA)     

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+?/? 28 c.3610C>A r.(?) p.(Pro1204Thr) MyTH4 1 (1017-1253) Unknown ACMG VUS g.76900495C>A g.77189450C>A - - MYO7A_000484 Heterozygous PubMed: Besnard, Garcia-Garcia 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Besnard, Garcia-Garcia 2014 Proband - - Spain - - - - - 1 Anne-Françoise Roux
+?/. - c.3610C>A r.(?) p.(Pro1204Thr) - Parent #1 - likely pathogenic g.76900495C>A g.77189450C>A MYO7A, variant 1: c.494C>T/p.T165M, variant 2: c.3610C>A/p.P1204T - MYO7A_000484 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET6 targeted sequencing panel - see paper retinal disease 690 PubMed: Weisschuh 2020 Filing key number: 249, Usher syndrome type 2, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
+?/. 28 c.3610C>A r.(?) p.(Pro1204Thr) - Unknown - likely pathogenic g.76900495C>A - c.3610C>A - MYO7A_000484 - PubMed: Colombo-2020 - - Germline - - - - - DNA SEQ - - retinal disease - PubMed: Colombo-2020 - M no - - - - - - 1 LOVD
+/. 28 c.3610C>A r.(?) p.(Pro1204Thr) - Parent #1 - pathogenic g.76900495C>A - c.3610C>A - MYO7A_000484 - PubMed: Galbis-Martinez-2021 - - Germline - - - - - DNA ? - - retinal disease - PubMed: Galbis-Martinez-2021 - - - - - - - - - 4 LOVD
+?/. - c.3610C>A r.(?) p.(Pro1204Thr) - Unknown - likely pathogenic g.76900495C>A - - - MYO7A_000484 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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