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.

31 entries on 1 page. Showing entries 1 - 31.
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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)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/+ 39 c.5392C>T r.(?) p.(Gln1798*) MyTH4 2 (1747-1896) Parent #2 - pathogenic g.76915186C>T g.77204141C>T - - MYO7A_000028 Heterozygous PubMed: Roux 2006 - - Germline - - +BfaI - - DNA SEQ - - USH1B ? PubMed: Roux 2006 Proband M - France - - - - - 1 Anne-Françoise Roux
+/+ 39 c.5392C>T r.(?) p.(Gln1798*) MyTH4 2 (1747-1896) Parent #1 - pathogenic g.76915186C>T g.77204141C>T - - MYO7A_000028 Heterozygous PubMed: Roux 2011 - - Germline - - +BfaI - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband F - France - - - - - 1 Anne-Françoise Roux
+/+ 39 c.5392C>T r.(?) p.(Gln1798*) MyTH4 2 (1747-1896) Parent #2 - pathogenic g.76915186C>T g.77204141C>T - - MYO7A_000028 Heterozygous PubMed: Pennings 2004 - - Germline - - +BfaI - - DNA SEQ - - USH1B ? PubMed: Pennings 2004 Proband - - Netherlands - - - - - 1 Anne-Françoise Roux
+/+ 39 c.5392C>T r.(?) p.(Gln1798*) MyTH4 2 (1747-1896) Parent #1 - pathogenic g.76915186C>T g.77204141C>T - - MYO7A_000028 Heterozygous PubMed: Pennings 2004 - - Germline - - +BfaI - - DNA SEQ - - USH1B ? PubMed: Pennings 2004 Proband - - Netherlands - - - - - 1 Anne-Françoise Roux
+/+ 39 c.5392C>T r.(?) p.(Gln1798*) MyTH4 2 (1747-1896) Parent #1 - pathogenic g.76915186C>T g.77204141C>T - - MYO7A_000028 Heterozygous PubMed: Pennings 2004 - - Germline - - +BfaI - - DNA SEQ - - USH1B ? PubMed: Pennings 2004 Relative - - Netherlands - - - - - 1 Anne-Françoise Roux
+/+ 39 c.5392C>T r.(?) p.(Gln1798*) MyTH4 2 (1747-1896) Parent #2 - pathogenic g.76915186C>T g.77204141C>T - - MYO7A_000028 Heterozygous PubMed: Bharadwaj 2000 - - Germline - - +BfaI - - DNA SEQ - - USH1B ? PubMed: Bharadwaj 2000 Proband - - United Kingdom (Great Britain) - - - - - 1 Anne-Françoise Roux
+/+ 39 c.5392C>T r.(?) p.(Gln1798*) MyTH4 2 (1747-1896) Unknown - pathogenic g.76915186C>T g.77204141C>T - - MYO7A_000028 Heterozygous PubMed: Bharadwaj 2000 - - Germline - - +BfaI - - DNA SEQ - - USH1B ? PubMed: Bharadwaj 2000 Proband - - Germany - - - - - 1 Anne-Françoise Roux
+/+ 39 c.5392C>T r.(?) p.(Gln1798*) MyTH4 2 (1747-1896) Unknown - pathogenic g.76915186C>T g.77204141C>T - - MYO7A_000028 Heterozygous PubMed: Jacobson 2008 - - Germline - - +BfaI - - DNA SEQ - - USH1B ? PubMed: Jacobson 2008 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 39 c.5392C>T r.(?) p.(Gln1798*) MyTH4 2 (1747-1896) Parent #2 - pathogenic g.76915186C>T g.77204141C>T - - MYO7A_000028 Heterozygous PubMed: Janecke 1999, PubMed: Dad 2016 - - Germline - - +BfaI - - DNA SEQ - - USH1B ? PubMed: Janecke 1999, PubMed: Dad 2016 Proband - - - - - - - - 1 Anne-Françoise Roux
+/+ 39 c.5392C>T r.(?) p.(Gln1798*) MyTH4 2 (1747-1896) Parent #2 - pathogenic g.76915186C>T g.77204141C>T - - MYO7A_000028 Heterozygous PubMed: Roux 2011 - - Germline - - +BfaI - - DNA SEQ - - DFNB ? PubMed: Roux 2011 Proband M - France - - - - - 1 Anne-Françoise Roux
+/+ 39 c.5392C>T r.(?) p.(Gln1798*) MyTH4 2 (1747-1896) Unknown - pathogenic g.76915186C>T g.77204141C>T - - MYO7A_000028 Heterozygous PubMed: Roux 2011 - - Germline - - +BfaI - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband F - France - - - - - 1 Anne-Françoise Roux
+/+ 39 c.5392C>T r.(?) p.(Gln1798*) MyTH4 2 (1747-1896) Parent #1 - pathogenic g.76915186C>T g.77204141C>T - - MYO7A_000028 Heterozygous PubMed: Bonnet 2011 - - Germline - - +BfaI - - DNA SEQ - - USH1B ? PubMed: Bonnet 2011 Proband - - - - - - - - 1 Anne-Françoise Roux
+/+ 39 c.5392C>T r.(?) p.(Gln1798*) MyTH4 2 (1747-1896) Parent #1 - pathogenic g.76915186C>T g.77204141C>T - - MYO7A_000028 Heterozygous PubMed: Bonnet 2011 - - Germline - - +BfaI - - DNA SEQ - - USH1B ? PubMed: Bonnet 2011 Proband - - - - - - - - 1 Anne-Françoise Roux
+/+ 39 c.5392C>T r.(?) p.(Gln1798*) MyTH4 2 (1747-1896) Parent #1 - pathogenic g.76915186C>T g.77204141C>T - - MYO7A_000028 Heterozygous PubMed: Aparisi 2014 - - Germline - - +BfaI - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Aparisi 2014 Proband - - Spain - - - - - 1 Anne-Françoise Roux
+/+ 39 c.5392C>T r.(?) p.(Gln1798*) MyTH4 2 (1747-1896) Paternal (inferred) - pathogenic g.76915186C>T g.77204141C>T - - MYO7A_000028 Homozygous; mutation PubMed: Bonnet 2016 - rs397516317 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband M - Spain - - - - - 1 Crystel Bonnet
+/+ 39 c.5392C>T r.(?) p.(Gln1798*) MyTH4 2 (1747-1896) Maternal (inferred) - pathogenic g.76915186C>T g.77204141C>T - - MYO7A_000028 Homozygous; mutation PubMed: Bonnet 2016 - rs397516317 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband M - Spain - - - - - 1 Crystel Bonnet
+/+ 39 c.5392C>T r.(?) p.(Gln1798*) MyTH4 2 (1747-1896) Parent #2 - pathogenic g.76915186C>T g.77204141C>T - - MYO7A_000028 Heterozygous; mutation PubMed: Bonnet 2016 - rs397516317 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband F - France - - - - - 1 Crystel Bonnet
+/+ 39 c.5392C>T r.(?) p.(Gln1798*) MyTH4 2 (1747-1896) Parent #1 - pathogenic g.76915186C>T g.77204141C>T - - MYO7A_000028 Heterozygous; mutation PubMed: Bonnet 2016 - rs397516317 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband M - France - - - - - 1 Crystel Bonnet
+/. - c.5392C>T r.(?) p.(Gln1798Ter) - Unknown - pathogenic g.76915186C>T g.77204141C>T MYO7A(NM_000260.3):c.5392C>T (p.Q1798*) - MYO7A_000028 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.5392C>T r.(?) p.(Gln1798Ter) - Unknown - pathogenic g.76915186C>T g.77204141C>T MYO7A(NM_000260.3):c.5392C>T (p.Q1798*) - MYO7A_000028 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.5392C>T r.(?) p.(Gln1798*) - Parent #1 - pathogenic (recessive) g.76915186C>T g.77204141C>T - - MYO7A_000028 - PubMed: Fuster-Garcia 2018 - - Germline - - - - - DNA arraySEQ - - retinal disease RP1967 PubMed: Fuster-Garcia 2018 analysis 77 USH patients - - Spain - - - - - 1 Global Variome, with Curator vacancy
+?/. - c.5392C>T r.(?) p.(Gln1798*) - Parent #1 - likely pathogenic g.76915186C>T g.77204141C>T - - MYO7A_000028 - PubMed: Stone 2017 - - Germline - - - - - DNA SEQ-NG - - retinal disease 526 PubMed: Stone 2017 1 affected M - (United States) - - - - - 1 LOVD
+?/. - c.5392C>T r.(?) p.(Gln1798*) - Parent #2 - likely pathogenic g.76915186C>T g.77204141C>T - - MYO7A_000028 - PubMed: Stone 2017 - - Germline - - - - - DNA SEQ-NG - - retinal disease 524 PubMed: Stone 2017 1 affected F - (United States) - - - - - 1 LOVD
+/. 39 c.5392C>T r.(?) p.(Gln1798*) - Parent #2 - pathogenic (recessive) g.76915186C>T g.77204141C>T - - MYO7A_000028 - PubMed: Cremers 2007 - - Germline - - - - - DNA PE - - retinal disease USH1-18 PubMed: Cremers 2007 - M no Denmark - - - - - 1 LOVD
+/. - c.5392C>T r.(?) p.(Gln1798Ter) - Both (homozygous) ACMG pathogenic g.76915186C>T - - - MYO7A_000028 - PubMed: Mansard et al, 2021 - rs397516317 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - M - - - - - - - 1 Anne-Françoise Roux
+?/. - c.5392C>T r.(?) p.(Gln1798*) - Both (homozygous) - likely pathogenic g.76915186C>T g.77204141C>T MYO7A c.5392C >T p.(Gln1798*) - MYO7A_000028 homozygous PubMed: Méjécase 2020 - - Unknown ? - - - - DNA SEQ-NG - retrospective case note review, targeted gene panel testing retinal disease 38 {PMID:Méjécase 2020:3278337 - ? - United Arab Emirates - - - - - 1 LOVD
+?/. 39 c.5392C>T r.(?) p.(Gln1798*) - Unknown - likely pathogenic g.76915186C>T - c.5392C>T,p.Q1798X - MYO7A_000028 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
+?/. 39 c.5392C>T r.(?) p.(Gln1798*) - Parent #2 - likely pathogenic (recessive) g.76915186C>T - c.5392C>T p.Gln1798* - MYO7A_000028 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease CIC08100 PubMed: Khateb 2020 multiple affected subjects F - - French - - - - 1 LOVD
+?/. 39 c.5392C>T r.(?) p.(Gln1798*) - Parent #2 - likely pathogenic (recessive) g.76915186C>T - c.5392C>T p.Gln1798* - MYO7A_000028 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease CIC07979 PubMed: Khateb 2020 multiple affected subjects F - - French - - - - 1 LOVD
+?/. 39 c.5392C>T r.(?) p.(Gln1798*) - Both (homozygous) - likely pathogenic (recessive) g.76915186C>T - c.5392C>T - MYO7A_000028 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease 1373446 PubMed: Khateb 2020 - M - - - - - - - 1 LOVD
+/. 39 c.5392C>T r.(?) p.(Gln1798*) - Parent #1 - pathogenic g.76915186C>T - c.5392C>T - MYO7A_000028 - PubMed: Galbis-Martinez-2021 - - Germline - - - - - DNA ? - - retinal disease - PubMed: Galbis-Martinez-2021 - - - - - - - - - 4 LOVD
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