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.

24 entries on 1 page. Showing entries 1 - 24.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

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Re-site     

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Methylation     

Template     

Technique     

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Disease     

ID_report     

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Data_av     

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Owner     
+/+ 3 c.52C>T r.(?) p.(Gln18*) - Paternal (inferred) - pathogenic g.76853788C>T g.77142742C>T - - MYO7A_000279 Homozygous PubMed: Zhou 2012 - - Germline - - - - - DNA SEQ - - USH1B ? PubMed: Zhou 2012 Proband M - Canada - - - - - 1 Anne-Françoise Roux
+/+ 3 c.52C>T r.(?) p.(Gln18*) - Maternal (inferred) - pathogenic g.76853788C>T g.77142742C>T - - MYO7A_000279 Homozygous PubMed: Zhou 2012 - - Germline - - - - - DNA SEQ - - USH1B ? PubMed: Zhou 2012 Proband M - Canada - - - - - 1 Anne-Françoise Roux
+/+ 3 c.52C>T r.(?) p.(Gln18*) - Paternal (inferred) - pathogenic g.76853788C>T g.77142742C>T - - MYO7A_000279 Homozygous PubMed: Zhou 2012 - - Germline - - - - - DNA SEQ - - USH1B ? PubMed: Zhou 2012 Proband M - Canada - - - - - 1 Anne-Françoise Roux
+/+ 3 c.52C>T r.(?) p.(Gln18*) - Maternal (inferred) - pathogenic g.76853788C>T g.77142742C>T - - MYO7A_000279 Homozygous PubMed: Zhou 2012 - - Germline - - - - - DNA SEQ - - USH1B ? PubMed: Zhou 2012 Proband M - Canada - - - - - 1 Anne-Françoise Roux
+/+ 3 c.52C>T r.(?) p.(Gln18*) - Paternal (inferred) - pathogenic g.76853788C>T g.77142742C>T - - MYO7A_000279 Homozygous PubMed: Zhou 2012 - - Germline - - - - - DNA SEQ - - USH1B ? PubMed: Zhou 2012 Proband F - Canada - - - - - 1 Anne-Françoise Roux
+/+ 3 c.52C>T r.(?) p.(Gln18*) - Maternal (inferred) - pathogenic g.76853788C>T g.77142742C>T - - MYO7A_000279 Homozygous PubMed: Zhou 2012 - - Germline - - - - - DNA SEQ - - USH1B ? PubMed: Zhou 2012 Proband F - Canada - - - - - 1 Anne-Françoise Roux
+/+ 3 c.52C>T r.(?) p.(Gln18*) - Paternal (inferred) - pathogenic g.76853788C>T g.77142742C>T - - MYO7A_000279 Homozygous PubMed: Zhou 2012 - - Germline - - - - - DNA SEQ - - USH1B ? PubMed: Zhou 2012 Relative F - Canada - - - - - 1 Anne-Françoise Roux
+/+ 3 c.52C>T r.(?) p.(Gln18*) - Maternal (inferred) - pathogenic g.76853788C>T g.77142742C>T - - MYO7A_000279 Homozygous PubMed: Zhou 2012 - - Germline - - - - - DNA SEQ - - USH1B ? PubMed: Zhou 2012 Relative F - Canada - - - - - 1 Anne-Françoise Roux
+/+ 3 c.52C>T r.(?) p.(Gln18*) - Paternal (confirmed) - pathogenic g.76853788C>T g.77142742C>T - - MYO7A_000279 Heterozygous PubMed: Yoshimura 2012 - - Germline - 0/380 controls - - - DNA SEQ - - USH1B ? PubMed: Yoshimura 2012 Proband M - Japan - - - - - 1 Anne-Françoise Roux
+/+ 3 c.52C>T r.(?) p.(Gln18*) - Parent #2 - pathogenic g.76853788C>T g.77142742C>T - - MYO7A_000279 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband - - Slovenia - - - - - 1 Crystel Bonnet
+/+ 3 c.52C>T r.(?) p.(Gln18*) - Parent #1 - pathogenic g.76853788C>T g.77142742C>T - - MYO7A_000279 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband - - Slovenia - - - - - 1 Crystel Bonnet
+/+ 3 c.52C>T r.(?) p.(Gln18*) - Parent #1 - pathogenic g.76853788C>T g.77142742C>T - - MYO7A_000279 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband - - Slovenia - - - - - 1 Crystel Bonnet
+/+ 3 c.52C>T r.(?) p.(Gln18*) - Parent #1 - pathogenic g.76853788C>T g.77142742C>T - - MYO7A_000279 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband - - Slovenia - - - - - 1 Crystel Bonnet
+/+ 3 c.52C>T r.(?) p.(Gln18*) - Paternal (inferred) - pathogenic g.76853788C>T g.77142742C>T - - MYO7A_000279 Homozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband - - Slovenia - - - - - 1 Crystel Bonnet
+/+ 3 c.52C>T r.(?) p.(Gln18*) - Maternal (inferred) - pathogenic g.76853788C>T g.77142742C>T - - MYO7A_000279 Homozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband - - Slovenia - - - - - 1 Crystel Bonnet
+/+ 3 c.52C>T r.(?) p.(Gln18*) - Paternal (inferred) - pathogenic g.76853788C>T g.77142742C>T - - MYO7A_000279 Homozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband - - Slovenia - - - - - 1 Crystel Bonnet
+/+ 3 c.52C>T r.(?) p.(Gln18*) - Maternal (inferred) - pathogenic g.76853788C>T g.77142742C>T - - MYO7A_000279 Homozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband - - Slovenia - - - - - 1 Crystel Bonnet
+/. 3 c.52C>T r.(?) p.(Gln18*) - Both (homozygous) - pathogenic (recessive) g.76853788C>T - - - MYO7A_000279 - PubMed: Ivanova 2018 - - Germline - - - - - DNA SEQ-NG-S - - USH1B Pat2 PubMed: Ivanova 2018 - M - Ukraine - - - - - 1 Vladimir Strelnikov
+/. 3 c.52C>T r.(?) p.(Gln18*) - Both (homozygous) - pathogenic (recessive) g.76853788C>T - - - MYO7A_000279 - PubMed: Ivanova 2018 - - Germline - - - - - DNA SEQ-NG-S - - USH1B Pat15 PubMed: Ivanova 2018 Proband F - Russian Federation Slavonian - - - - 1 Vladimir Strelnikov
+/. 3 c.52C>T r.(?) p.(Gln18*) - Parent #2 - pathogenic (recessive) g.76853788C>T - - - MYO7A_000279 - PubMed: Ivanova 2018 - - Germline - - - - - DNA SEQ-NG-S - - USH1B Pat21 PubMed: Ivanova 2018 Proband M - Russian Federation Slavonian - - - - 1 Vladimir Strelnikov
+/. - c.52C>T r.(?) p.(Gln18Ter) - Paternal (confirmed) ACMG pathogenic g.76853788C>T - - - MYO7A_000279 - PubMed: Mansard et al, 2021 - rs1555051455 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - ? - - - - - - - 1 Anne-Françoise Roux
+?/. - c.52C>T r.(?) p.(Gln18*) - Parent #1 - likely pathogenic g.76853788C>T g.77142742C>T MYO7A, variant 1: c.52C>T/p.Q18*, variant 2: c.3719G>A/p.R1240Q - MYO7A_000279 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET8 targeted sequencing panel - see paper retinal disease 159 PubMed: Weisschuh 2020 Filing key number: 65, Usher syndrome type I, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
+/. - c.52C>T r.(?) p.(Gln18Ter) - Unknown ACMG pathogenic g.76853788C>T g.77142742C>T MYO7A c.C52T, p.Q18X - MYO7A_000279 marked as causative, heterozygous PubMed: Ma 2021 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ - whole exome sequencing retinal disease 54 PubMed: Ma 2021 - ? - Korea - - - - - 1 LOVD
+/. - c.52C>T r.(?) p.(Gln18Ter) - Unknown ACMG pathogenic g.76853788C>T g.77142742C>T MYO7A c.C52T, p.Q18X - MYO7A_000279 marked as causative, heterozygous PubMed: Ma 2021 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ - whole exome sequencing retinal disease 174 PubMed: Ma 2021 - ? - Korea - - - - - 1 LOVD
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