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.

6 entries on 1 page. Showing entries 1 - 6.
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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     
-/- 48i c.6558+25A>G r.(=) p.(=) - Unknown - benign g.76925049A>G g.77214004A>G - - MYO7A_000115 Heterozygous; Neutral PubMed: Le Quesne Stabej 2012 - - Germline - 0/96 controls +PspGI;+BssKI;+ScrFI;+StyD4I;+BstNI;-BfaI; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/- 48i c.6558+25A>G r.(=) p.(=) - Unknown - benign g.76925049A>G g.77214004A>G - - MYO7A_000115 Heterozygous; Neutral PubMed: Le Quesne Stabej 2012 - - Germline - 0/96 controls +PspGI;+BssKI;+ScrFI;+StyD4I;+BstNI;-BfaI; - - DNA SEQ - - USH - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/- 48i c.6558+25A>G r.(=) p.(=) - Unknown - benign g.76925049A>G g.77214004A>G - - MYO7A_000115 Heterozygous PubMed: Roux 2011 - - Germline - - +PspGI;+BssKI;+ScrFI;+StyD4I;+BstNI;-BfaI; - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband F - France - - - - - 1 Anne-Françoise Roux
-/- 48i c.6558+25A>G r.(=) p.(=) - Unknown - benign g.76925049A>G g.77214004A>G - - MYO7A_000115 Heterozygous PubMed: Jaijo 2006 - - Germline - - +PspGI;+BssKI;+ScrFI;+StyD4I;+BstNI;-BfaI; - - DNA minigene, SEQ - - USH1B ? PubMed: Jaijo 2006 Relative F - Spain - - - - - 1 Jose Maria Millan
-/- 48i c.6558+25A>G r.(=) p.(=) - Paternal (inferred) - benign g.76925049A>G g.77214004A>G - - MYO7A_000115 Homozygous PubMed: Jaijo 2006 - - Germline - - +PspGI;+BssKI;+ScrFI;+StyD4I;+BstNI;-BfaI; - - DNA SEQ - - USH1B ? PubMed: Jaijo 2006 Proband F - Spain - - - - - 1 Jose Maria Millan
-/- 48i c.6558+25A>G r.(=) p.(=) - Maternal (inferred) - benign g.76925049A>G g.77214004A>G - - MYO7A_000115 Homozygous PubMed: Jaijo 2006 - - Germline - - +PspGI;+BssKI;+ScrFI;+StyD4I;+BstNI;-BfaI; - - DNA SEQ - - USH1B ? PubMed: Jaijo 2006 Proband F - Spain - - - - - 1 Jose Maria Millan
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