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.
Legend   How to query  

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     
+/+ 3 c.77C>A r.(?) p.(Ala26Glu) - Paternal (confirmed) - pathogenic g.76853813C>A g.77142767C>A - - MYO7A_000168 Heterozygous PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 1/874 controls +MnlI;-AciI; - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/+ 3 c.77C>A r.(?) p.(Ala26Glu) - Parent #1 - pathogenic g.76853813C>A g.77142767C>A - - MYO7A_000168 Heterozygous PubMed: Jaijo 2007; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA minigene, SEQ - - USH1B ? PubMed: Jaijo 2007 Proband - Minigene studies in Aparisi et al., 2013 M - Italy - - - - - 1 Jose Maria Millan
+/+ 3 c.77C>A r.(?) p.(Ala26Glu) - Unknown - pathogenic g.76853813C>A g.77142767C>A - - MYO7A_000168 Heterozygous PubMed: Bharadwaj 2000; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/172 controls - - - DNA SEQ - - USH1B ? PubMed: Bharadwaj 2000 Proband - - Italy - - - - - 1 Anne-Françoise Roux
+/+ 3 c.77C>A r.(?) p.(Ala26Glu) - Unknown - pathogenic g.76853813C>A g.77142767C>A - - MYO7A_000168 Heterozygous PubMed: Licastro 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Licastro 2012 Proband - - Italy - - - - - 1 Anne-Françoise Roux
+/+ 3 c.77C>A r.(?) p.(Ala26Glu) Motor domain (1-729) Parent #2 - pathogenic g.76853813C>A g.77142767C>A - - MYO7A_000168 Heterozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband M - Italy - - - - - 1 Crystel Bonnet
+/+ 3 c.77C>A r.(?) p.(Ala26Glu) Motor domain (1-729) Unknown - pathogenic g.76853813C>A g.77142767C>A - - MYO7A_000168 Heterozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband F - Italy - - - - - 1 Crystel Bonnet
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.