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.
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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     
+/+ 18 c.2115C>A r.(?) p.(Cys705*) Motor domain (1-729) Paternal (inferred) - pathogenic g.76886438C>A g.77175392C>A - - MYO7A_000511 Homozygous; possible pathogenic PubMed: Yoshimura 2014 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Yoshimura 2014 Proband - - Japan - - - - - 1 Anne-Françoise Roux
+/+ 18 c.2115C>A r.(?) p.(Cys705*) Motor domain (1-729) Maternal (inferred) - pathogenic g.76886438C>A g.77175392C>A - - MYO7A_000511 Homozygous; possible pathogenic PubMed: Yoshimura 2014 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Yoshimura 2014 Proband - - Japan - - - - - 1 Anne-Françoise Roux
+/. - c.2115C>A r.(?) p.(Cys705Ter) - Unknown ACMG pathogenic g.76886438C>A g.77175392C>A MYO7A c.C2115A, p.C705X - MYO7A_000511 marked as causative, heterozygous PubMed: Ma 2021 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ - whole exome sequencing retinal disease 54 PubMed: Ma 2021 - ? - Korea - - - - - 1 LOVD
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