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.

8 entries on 1 page. Showing entries 1 - 8.
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     
+/+ 42 c.5749G>T r.(?) p.(Glu1917*) FERM 2 (1902-2205) Unknown - pathogenic g.76918340G>T g.77207295G>T - - MYO7A_000362 Heterozygous PubMed: Jacobson 2008 - - Germline - - +DdeI;-BstBI;-TaqI; - - DNA SEQ - - USH1B ? PubMed: Jacobson 2008 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 42 c.5749G>T r.(?) p.(Glu1917*) FERM 2 (1902-2205) Parent #2 - pathogenic g.76918340G>T g.77207295G>T - - MYO7A_000362 Heterozygous PubMed: Bonnet 2011 - - Germline - - +DdeI;-BstBI;-TaqI; - - DNA SEQ - - USH1B ? PubMed: Bonnet 2011 Proband - - - - - - - - 1 Anne-Françoise Roux
+/+ 42 c.5749G>T r.(?) p.(Glu1917*) FERM 2 (1902-2205) Parent #2 - pathogenic g.76918340G>T g.77207295G>T - - MYO7A_000362 Heterozygous PubMed: Bonnet 2011 - - Germline - - +DdeI;-BstBI;-TaqI; - - DNA SEQ - - USH1B ? PubMed: Bonnet 2011 Proband - - - - - - - - 1 Anne-Françoise Roux
+/+ 42 c.5749G>T r.(?) p.(Glu1917*) FERM 2 (1902-2205) Unknown - pathogenic g.76918340G>T g.77207295G>T - - MYO7A_000362 Heterozygous PubMed: Aparisi 2014 - - Germline - - +DdeI;-BstBI;-TaqI; - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Aparisi 2014 Proband - - Spain - - - - - 1 Anne-Françoise Roux
+/. - c.5749G>T r.(?) p.(Glu1917*) - Parent #2 - pathogenic g.76918340G>T g.77207295G>T - - MYO7A_000362 - PubMed: Neuhaus 2017 - - Germline yes - - - - DNA SEQ-NG - gene panel USH Pat53 PubMed: Neuhaus 2017 - - no Germany - - - - - 1 LOVD
+/. - c.5749G>T r.(?) p.(Glu1917Ter) - Unknown ACMG pathogenic (recessive) g.76918340G>T g.77207295G>T - - MYO7A_000362 ACMG PM2, PVS1, PP5 PubMed: Weisschuh 2024 - - Germline - - - - - DNA SEQ-NG - WGS ? CRD-858 PubMed: Weisschuh 2024 patient, no family history M - Germany - - - - - 1 Johan den Dunnen
+/. - c.5749G>T r.(?) p.(Glu1917Ter) - Unknown ACMG pathogenic (recessive) g.76918340G>T g.77207295G>T - - MYO7A_000362 ACMG PM2, PVS1, PP5 PubMed: Weisschuh 2024 866518 - Germline - - - - - DNA SEQ-NG - WGS ? USHI-81 PubMed: Weisschuh 2024 patient M - Germany - - - - - 1 Johan den Dunnen
+/. - c.5749G>T r.(?) p.(Glu1917*) - Unknown - pathogenic g.76918340G>T - - - MYO7A_000362 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
Legend   How to query  


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