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.

23 entries on 1 page. Showing entries 1 - 23.
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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     
+/+ 9 c.999T>G r.(?) p.(Tyr333*) Motor domain (1-729) Parent #1 - pathogenic g.76869472T>G g.77158426T>G - - MYO7A_000126 Hemizygous PubMed: Roux 2011 - rs111033285 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 9 c.999T>G r.(?) p.(Tyr333*) Motor domain (1-729) Parent #2 - pathogenic g.76869472T>G g.77158426T>G - - MYO7A_000126 Heterozygous PubMed: Gerber 2006 - rs111033285 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Gerber 2006 Proband - - France - - - - - 1 Anne-Françoise Roux
+/+ 9 c.999T>G r.(?) p.(Tyr333*) Motor domain (1-729) Parent #1 - pathogenic g.76869472T>G g.77158426T>G - - MYO7A_000126 Heterozygous PubMed: Gerber 2006 - rs111033285 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Gerber 2006 Proband - - France - - - - - 1 Anne-Françoise Roux
+/+ 9 c.999T>G r.(?) p.(Tyr333*) Motor domain (1-729) Parent #1 - pathogenic g.76869472T>G g.77158426T>G - - MYO7A_000126 Heterozygous PubMed: Gerber 2006 - rs111033285 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Gerber 2006 Proband - - France - - - - - 1 Anne-Françoise Roux
+/+ 9 c.999T>G r.(?) p.(Tyr333*) Motor domain (1-729) Parent #2 - pathogenic g.76869472T>G g.77158426T>G - - MYO7A_000126 Heterozygous PubMed: Gerber 2006 - rs111033285 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Gerber 2006 Proband - - France - - - - - 1 Anne-Françoise Roux
+/+ 9 c.999T>G r.(?) p.(Tyr333*) Motor domain (1-729) Paternal (inferred) - pathogenic g.76869472T>G g.77158426T>G - - MYO7A_000126 Homozygous PubMed: Weston 1996 - rs111033285 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Weston 1996 Proband - - United States - - - - - 1 William J. Kimberling
+/+ 9 c.999T>G r.(?) p.(Tyr333*) Motor domain (1-729) Maternal (inferred) - pathogenic g.76869472T>G g.77158426T>G - - MYO7A_000126 Homozygous PubMed: Weston 1996 - rs111033285 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Weston 1996 Proband - - United States - - - - - 1 William J. Kimberling
+/+ 9 c.999T>G r.(?) p.(Tyr333*) Motor domain (1-729) Paternal (inferred) - pathogenic g.76869472T>G g.77158426T>G - - MYO7A_000126 Homozygous PubMed: Jacobson 2008 - rs111033285 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Jacobson 2008 Proband M - - - - - - - 1 Anne-Françoise Roux
+/+ 9 c.999T>G r.(?) p.(Tyr333*) Motor domain (1-729) Maternal (inferred) - pathogenic g.76869472T>G g.77158426T>G - - MYO7A_000126 Homozygous PubMed: Jacobson 2008 - rs111033285 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Jacobson 2008 Proband M - - - - - - - 1 Anne-Françoise Roux
+/+ 9 c.999T>G r.(?) p.(Tyr333*) Motor domain (1-729) Paternal (inferred) - pathogenic g.76869472T>G g.77158426T>G - - MYO7A_000126 Homozygous PubMed: Jacobson 2008 - rs111033285 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Jacobson 2008 Relative M - - - - - - - 1 Anne-Françoise Roux
+/+ 9 c.999T>G r.(?) p.(Tyr333*) Motor domain (1-729) Maternal (inferred) - pathogenic g.76869472T>G g.77158426T>G - - MYO7A_000126 Homozygous PubMed: Jacobson 2008 - rs111033285 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Jacobson 2008 Relative M - - - - - - - 1 Anne-Françoise Roux
+/+ 9 c.999T>G r.(?) p.(Tyr333*) Motor domain (1-729) Parent #1 - pathogenic g.76869472T>G g.77158426T>G - - MYO7A_000126 Heterozygous; mutation PubMed: Bonnet 2016 - rs111033285 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband M - France - - - - - 1 Crystel Bonnet
+/+ 9 c.999T>G r.(?) p.(Tyr333*) Motor domain (1-729) Maternal (confirmed) - pathogenic g.76869472T>G g.77158426T>G - - MYO7A_000126 Homozygous; mutation PubMed: Bonnet 2016 - rs111033285 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband F - Spain - - - - - 1 Crystel Bonnet
+/+ 9 c.999T>G r.(?) p.(Tyr333*) Motor domain (1-729) Paternal (confirmed) - pathogenic g.76869472T>G g.77158426T>G - - MYO7A_000126 Homozygous; mutation PubMed: Bonnet 2016 - rs111033285 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband F - Spain - - - - - 1 Crystel Bonnet
+/+ 9 c.999T>G r.(?) p.(Tyr333*) Motor domain (1-729) Maternal (confirmed) - pathogenic g.76869472T>G g.77158426T>G - - MYO7A_000126 Homozygous; mutation PubMed: Bonnet 2016 - rs111033285 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband M - Spain - - - - - 1 Crystel Bonnet
+/+ 9 c.999T>G r.(?) p.(Tyr333*) Motor domain (1-729) Paternal (confirmed) - pathogenic g.76869472T>G g.77158426T>G - - MYO7A_000126 Homozygous; mutation PubMed: Bonnet 2016 - rs111033285 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband M - Spain - - - - - 1 Crystel Bonnet
+/+ 9 c.999T>G r.(?) p.(Tyr333*) Motor domain (1-729) Maternal (confirmed) - pathogenic g.76869472T>G g.77158426T>G - - MYO7A_000126 Homozygous; mutation PubMed: Bonnet 2016 - rs111033285 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband M - Spain - - - - - 1 Crystel Bonnet
+/+ 9 c.999T>G r.(?) p.(Tyr333*) Motor domain (1-729) Paternal (confirmed) - pathogenic g.76869472T>G g.77158426T>G - - MYO7A_000126 Homozygous; mutation PubMed: Bonnet 2016 - rs111033285 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband M - Spain - - - - - 1 Crystel Bonnet
+/+ 9 c.999T>G r.(?) p.(Tyr333*) Motor domain (1-729) Maternal (confirmed) - pathogenic g.76869472T>G g.77158426T>G - - MYO7A_000126 Homozygous; mutation PubMed: Bonnet 2016 - rs111033285 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband F - Spain - - - - - 1 Crystel Bonnet
+/+ 9 c.999T>G r.(?) p.(Tyr333*) Motor domain (1-729) Paternal (confirmed) - pathogenic g.76869472T>G g.77158426T>G - - MYO7A_000126 Homozygous; mutation PubMed: Bonnet 2016 - rs111033285 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband F - Spain - - - - - 1 Crystel Bonnet
+?/. - c.999T>G r.(?) p.(Tyr333*) - Both (homozygous) - likely pathogenic g.76869472T>G g.77158426T>G MYO7A c.999T>G, p.Y333X - MYO7A_000126 homozygous PubMed: Jauregui 2020 - - Unknown ? - - - - DNA SEQ-NG blood targeted sequencing retinal disease 139 PubMed: Jauregui 2020 - F - (United States) Hispanic - - - - 1 LOVD
+?/. - c.999T>G r.(?) p.(Tyr333*) - Parent #2 - likely pathogenic g.76869472T>G g.77158426T>G MYO7A c.999T>G, p.Y333X - MYO7A_000126 compound heterozygous PubMed: Jauregui 2020 - - Unknown ? - - - - DNA SEQ-NG blood targeted sequencing retinal disease 138 PubMed: Jauregui 2020 - M - (United States) Hispanic - - - - 1 LOVD
+/. - c.999T>G r.(?) p.(Tyr333Ter) - Unknown ACMG pathogenic g.76869472T>G - - - MYO7A_000126 - PubMed: Mansard et al, 2021 - rs111033285 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
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