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.

3 entries on 1 page. Showing entries 1 - 3.
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     
+?/? 20 c.2311G>T r.(?) p.(Ala771Ser) IQ 2 (768-788) Maternal (confirmed) ACMG VUS g.76890119G>T g.77179073G>T - - MYO7A_000352 Heterozygous; possible pathogenic PubMed: Yoshimura 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - -Fnu4HI;-ApeKI;-BbvI;-TseI; - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Yoshimura 2014 Proband - - Japan - - - - - 1 Anne-Françoise Roux
+?/? 20 c.2311G>T r.(?) p.(Ala771Ser) IQ 2 (768-788) Unknown ACMG VUS g.76890119G>T g.77179073G>T - - MYO7A_000352 Heterozygous; probable pathogenic PubMed: Nakanishi 2010; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/270 controls -Fnu4HI;-ApeKI;-BbvI;-TseI; - - DNA SEQ - - USH1B ? PubMed: Nakanishi 2010 Proband M - Japan - - - - - 1 Anne-Françoise Roux
?/. - c.2311G>T r.(?) p.(Ala771Ser) - Unknown ACMG VUS g.76890119G>T g.77179073G>T MYO7A c.G2311T, p.A771S - MYO7A_000352 marked as possibly causative, single heterozygous change in a recessive gene, heterozygous PubMed: Ma 2021 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ - whole exome sequencing retinal disease 156 PubMed: Ma 2021 - ? - Korea - - - - - 1 LOVD
Legend   How to query  


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