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.

12 entries on 1 page. Showing entries 1 - 12.
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     
+?/? 23 c.2863G>A r.(?) p.(Gly955Ser) - Parent #2 ACMG VUS g.76892594G>A g.77181548G>A - - MYO7A_000133 Heterozygous PubMed: Levy 1997; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/100 controls - - - DNA SEQ - - USH1B ? PubMed: Levy 1997 Proband - - - - - - - - 1 Anne-Françoise Roux
+?/? 23 c.2863G>A r.(?) p.(Gly955Ser) - Parent #2 ACMG VUS g.76892594G>A g.77181548G>A - - MYO7A_000133 Heterozygous PubMed: Levy 1997; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/100 controls - - - DNA SEQ - - USH1B ? PubMed: Levy 1997 Relative - - - - - - - - 1 Anne-Françoise Roux
+?/? 23 c.2863G>A r.(?) p.(Gly955Ser) - Parent #1 ACMG VUS g.76892594G>A g.77181548G>A - - MYO7A_000133 Heterozygous PubMed: Jacobson 2009; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ - - USH1B ? PubMed: Jacobson 2009 Proband M - - - - - - - 1 William J. Kimberling
+?/? 23 c.2863G>A r.(?) p.(Gly955Ser) - Paternal (inferred) ACMG VUS g.76892594G>A g.77181548G>A - - MYO7A_000133 Homozygous; mutation PubMed: Reddy 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Reddy 2014 Proband M - Egypt - - - - - 1 Rima Slim
+?/? 23 c.2863G>A r.(?) p.(Gly955Ser) - Maternal (inferred) ACMG VUS g.76892594G>A g.77181548G>A - - MYO7A_000133 Homozygous; mutation PubMed: Reddy 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Reddy 2014 Proband M - Egypt - - - - - 1 Rima Slim
+?/? 23 c.2863G>A r.(?) p.(Gly955Ser) - Paternal (inferred) ACMG VUS g.76892594G>A g.77181548G>A - - MYO7A_000133 Homozygous; mutation PubMed: Reddy 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ - - USH1B ? PubMed: Reddy 2014 Relative M - Egypt - - - - - 1 Rima Slim
+?/? 23 c.2863G>A r.(?) p.(Gly955Ser) - Maternal (inferred) ACMG VUS g.76892594G>A g.77181548G>A - - MYO7A_000133 Homozygous; mutation PubMed: Reddy 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ - - USH1B ? PubMed: Reddy 2014 Relative M - Egypt - - - - - 1 Rima Slim
+?/+ 23 c.2863G>A r.(?) p.(Gly955Ser) - Parent #2 ACMG VUS g.76892594G>A g.77181548G>A - - MYO7A_000133 Heterozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+?/. - c.2863G>A r.(?) p.(Gly955Ser) - Unknown - likely pathogenic g.76892594G>A g.77181548G>A - - MYO7A_000133 - PubMed: Ellingford 2016 - - Germline - - - - - DNA SEQ - 105-gene panel retinal disease 13005796 PubMed: Ellingford 2016 patient - - - - - - - - 1 LOVD
+?/. 23 c.2863G>A r.(?) p.(Gly955Ser) - Parent #1 - likely pathogenic (recessive) g.76892594G>A - c.2863G>A - MYO7A_000133 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease CIC04452 PubMed: Khateb 2020 One affected brother and one affected daughter M - - Father- French/ Mother-Sweden - - - - 1 LOVD
+?/. 23 c.2863G>A r.(?) p.(Gly955Ser) - Parent #2 - likely pathogenic (recessive) g.76892594G>A - c.2863G>A p.Gly955Ser - MYO7A_000133 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease CIC04290 PubMed: Khateb 2020 one affected brother F - - Father French and Mother Sweden - - - - 1 LOVD
+?/. - c.2863G>A r.(?) p.(Gly955Ser) - Unknown - likely pathogenic g.76892594G>A - - - MYO7A_000133 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.