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     
+?/? 31 c.3979G>A r.3979g>a p.Glu1327Lys FERM 1 (1258-1602) Parent #2 ACMG VUS g.76903150G>A g.77192105G>A - - MYO7A_000057 Heterozygous; No effect on splicing PubMed: Roux 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - +HpyCH4V - - DNA, RNA RT-PCR, SEQ - - USH1B ? PubMed: Roux 2011 Proband F - France - - - - - 1 Anne-Françoise Roux
+?/? 31 c.3979G>A r.(3979g>a) p.(Glu1327Lys) FERM 1 (1258-1602) Parent #1 ACMG VUS g.76903150G>A g.77192105G>A - - MYO7A_000057 Heterozygous PubMed: Najera 2002; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/200 controls +HpyCH4V - - DNA SEQ - - USH1B ? PubMed: Najera 2002 Proband M - Spain - - - - - 1 Jose Maria Millan
+?/? 31 c.3979G>A r.3979g>a p.Glu1327Lys FERM 1 (1258-1602) Unknown ACMG VUS g.76903150G>A g.77192105G>A - - MYO7A_000057 Heterozygous; No effect on splicing PubMed: Roux 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - +HpyCH4V - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband F - France - - - - - 1 Anne-Françoise Roux
+?/? 31 c.3979G>A r.3979g>a p.Glu1327Lys FERM 1 (1258-1602) Parent #2 ACMG VUS g.76903150G>A g.77192105G>A - - MYO7A_000057 Heterozygous PubMed: Sodi 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - +HpyCH4V - - DNA SEQ - - USH2 ? PubMed: Sodi 2014 Proabnd - - Italy - - - - - 1 Anne-Françoise Roux
+?/. - c.3979G>A r.(?) p.(Glu1327Lys) - Unknown ACMG likely pathogenic g.76903150G>A - - - MYO7A_000057 - PubMed: Mansard et al, 2021 - rs373169422 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
+?/. - c.3979G>A r.(?) p.(Glu1327Lys) - Unknown ACMG likely pathogenic g.76903150G>A - - - MYO7A_000057 - PubMed: Mansard et al, 2021 - rs373169422 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - M - - - - - - - 1 Anne-Françoise Roux
+/. 31 c.3979G>A r.(?) p.(Glu1327Lys) - Parent #2 - pathogenic g.76903150G>A - c.3979G>A - MYO7A_000057 - PubMed: Galbis-Martinez-2021 - - Germline - - - - - DNA ? - - retinal disease - PubMed: Galbis-Martinez-2021 - - - - - - - - - 4 LOVD
+/. 31 c.3979G>A r.(?) p.(Glu1327Lys) - Parent #2 - pathogenic g.76903150G>A - c.3979G>A - MYO7A_000057 - PubMed: Galbis-Martinez-2021 - - Germline - - - - - DNA ? - - retinal disease - PubMed: Galbis-Martinez-2021 - - - - - - - - - 4 LOVD
Legend   How to query  


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