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.

2 entries on 1 page. Showing entries 1 - 2.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

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DNA change (hg38)     

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-/? 49 c.6640G>A r.(?) p.(Gly2214Ser) - Paternal (confirmed) ACMG likely benign g.76925733G>A g.77214688G>A - - MYO7A_000388 Heterozygous; UV1 PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033231 Germline - 1/876 controls +ApeKI;+BbvI;+TseI;-BsrBI;-AciI; - - DNA SEQ - - USH2 ? PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/? 49 c.6640G>A r.(?) p.(Gly2214Ser) - Paternal (inferred) ACMG likely benign g.76925733G>A g.77214688G>A - - MYO7A_000388 Heterozygous; UV1 PubMed: Neveling 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033231 Germline - - +ApeKI;+BbvI;+TseI;-BsrBI;-AciI; - - DNA SEQ, SEQ-NG-S - - RPar ? PubMed: Neveling 2012 Proband M - - - - - - - 1 Anne-Françoise Roux
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