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.

8 entries on 1 page. Showing entries 1 - 8.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

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DNA change (genomic) (hg19)     

DNA change (hg38)     

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DB-ID     

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Reference     

ClinVar ID     

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Disease     

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Owner     
+?/? 42 c.5824G>A r.(?) p.(Gly1942Arg) FERM 2 (1902-2205) Paternal (inferred) ACMG VUS g.76918415G>A g.77207370G>A - - MYO7A_000358 Homozygous; Mutation PubMed: Duman 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033192 Germline - 0/192 controls -MnlI - - DNA SEQ - - DFNB ? PubMed: Duman 2011 Proband - - Turkey - - - - - 1 Anne-Françoise Roux
+?/? 42 c.5824G>A r.(?) p.(Gly1942Arg) FERM 2 (1902-2205) Maternal (inferred) ACMG VUS g.76918415G>A g.77207370G>A - - MYO7A_000358 Homozygous; Mutation PubMed: Duman 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033192 Germline - 0/192 controls -MnlI - - DNA SEQ - - DFNB ? PubMed: Duman 2011 Proband - - Turkey - - - - - 1 Anne-Françoise Roux
+?/? 42 c.5824G>A r.(?) p.(Gly1942Arg) FERM 2 (1902-2205) Paternal (inferred) ACMG VUS g.76918415G>A g.77207370G>A - - MYO7A_000358 Homozygous; Mutation PubMed: Duman 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033192 Germline - 0/192 controls -MnlI - - DNA SEQ - - DFNB ? PubMed: Duman 2011 Relative - - Turkey - - - - - 1 Anne-Françoise Roux
+?/? 42 c.5824G>A r.(?) p.(Gly1942Arg) FERM 2 (1902-2205) Maternal (inferred) ACMG VUS g.76918415G>A g.77207370G>A - - MYO7A_000358 Homozygous; Mutation PubMed: Duman 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033192 Germline - 0/192 controls -MnlI - - DNA SEQ - - DFNB ? PubMed: Duman 2011 Relative - - Turkey - - - - - 1 Anne-Françoise Roux
+?/? 42 c.5824G>A r.(?) p.(Gly1942Arg) FERM 2 (1902-2205) Paternal (inferred) ACMG VUS g.76918415G>A g.77207370G>A - - MYO7A_000358 Homozygous; Mutation PubMed: Duman 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033192 Germline - 0/192 controls -MnlI - - DNA SEQ - - DFNB ? PubMed: Duman 2011 Relative - - Turkey - - - - - 1 Anne-Françoise Roux
+?/? 42 c.5824G>A r.(?) p.(Gly1942Arg) FERM 2 (1902-2205) Maternal (inferred) ACMG VUS g.76918415G>A g.77207370G>A - - MYO7A_000358 Homozygous; Mutation PubMed: Duman 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033192 Germline - 0/192 controls -MnlI - - DNA SEQ - - DFNB ? PubMed: Duman 2011 Relative - - Turkey - - - - - 1 Anne-Françoise Roux
+?/+ 42 c.5824G>A r.(?) p.(Gly1942Arg) FERM2 (1902-2205) Parent #2 ACMG VUS g.76918415G>A g.77207370G>A - - MYO7A_000358 Heterozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033192 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband M - France - - - - - 1 Crystel Bonnet
?/. - c.5824G>A r.(?) p.(Gly1942Arg) - Both (homozygous) - VUS g.76918415G>A - - - MYO7A_000358 - PubMed: Roman 2020, Journal: Roman 2020 - - Germline - - - - - DNA SEQ, SEQ-NG - WES HL HL004 PubMed: Roman 2020, Journal: Roman 2020 new-born screening - - United States - - - - - 1 Johan den Dunnen
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