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     
+/+ 31 c.4117C>T r.(?) p.(Arg1373*) FERM 1 (1258-1602) Parent #1 - pathogenic g.76903288C>T g.77192243C>T - - MYO7A_000185 Heterozygous PubMed: Najera 2002 - - Germline - - -MwoI;-BstAPI; - - DNA SEQ - - USH1B ? PubMed: Najera 2002 Proband M - Spain - - - - - 1 Jose Maria Millan
+/+ 31 c.4117C>T r.(?) p.(Arg1373*) FERM 1 (1258-1602) Unknown - pathogenic g.76903288C>T g.77192243C>T - - MYO7A_000185 Heterozygous PubMed: Roux 2011 - - Germline - - -MwoI;-BstAPI; - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband F - France - - - - - 1 Anne-Françoise Roux
+/+ 31 c.4117C>T r.(?) p.(Arg1373*) FERM 1 (1258-1602) Maternal (confirmed) - pathogenic g.76903288C>T g.77192243C>T - - MYO7A_000185 Heterozygous PubMed: Baux, Vaché 2017 - - Germline - - -MwoI;-BstAPI; - - DNA SEQ, SEQ-NG-S - - DFNB S1763 PubMed: Baux 2017 Proband F - France - - - - - 1 Anne-Françoise Roux
+/. 31 c.4117C>T r.(?) p.(Arg1373*) - Parent #2 ACMG pathogenic (recessive) g.76903288C>T - - - MYO7A_000185 - - - - Germline yes - - - - DNA SEQ-NG-I - Exome sequencing USH Pat14 PubMed: Bahena 2021 - M no Mexico - - - - - 1 Barbara Vona
+/. 31 c.4117C>T r.(?) p.(Arg1373*) - Parent #2 - pathogenic g.76903288C>T - c.4117C>T - MYO7A_000185 - PubMed: Galbis-Martinez-2021 - - Germline - - - - - DNA ? - - retinal disease - PubMed: Galbis-Martinez-2021 - - - - - - - - - 4 LOVD
+/. - c.4117C>T r.(?) p.(Arg1373Ter) - Unknown ACMG pathogenic (recessive) g.76903288C>T g.77192243C>T - - MYO7A_000185 ACMG PM2, PVS1, PP5 PubMed: Weisschuh 2024 551138 - Germline - - - - - DNA SEQ-NG - WGS ? USHI-81 PubMed: Weisschuh 2024 patient M - Germany - - - - - 1 Johan den Dunnen
Legend   How to query  


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