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 (genomic) (hg19)     

DNA change (hg38)     

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Owner     
-?/? 44 c.6043T>C r.(?) p.(Tyr2015His) FERM 2 (1902-2205) Maternal (inferred) ACMG likely benign g.76919840T>C g.77208795T>C - - MYO7A_000217 Homozygous; UV2 PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/878 controls +BslI - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-?/? 44 c.6043T>C r.(?) p.(Tyr2015His) FERM 2 (1902-2205) Paternal (inferred) ACMG likely benign g.76919840T>C g.77208795T>C - - MYO7A_000217 Homozygous; UV2 PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/878 controls +BslI - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-?/? 44 c.6043T>C r.(?) p.(Tyr2015His) FERM 2 (1902-2205) Parent #2 ACMG likely benign g.76919840T>C g.77208795T>C - - MYO7A_000217 Heterozygous PubMed: Jacobson 2009; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - +BslI - - DNA SEQ - - USH1B ? PubMed: Jacobson 2009 Proband M - - - - - - - 1 William J. Kimberling
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