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.

18 entries on 1 page. Showing entries 1 - 18.
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.2904G>T r.(?) p.(Glu968Asp) - Unknown ACMG VUS g.76892635G>T g.77181589G>T - - MYO7A_000205 Heterozygous PubMed: Bujakowska 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033233 Germline - - -MnlI;-KpnI;-NlaIV;-BanI;-Acc65I; - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Bujakowska 2014 Proband - - United States - - - - - 1 Anne-Françoise Roux
+/? 23 c.2904G>T r.(?) p.(Glu968Asp) - Maternal (confirmed) ACMG VUS g.76892635G>T g.77181589G>T - - MYO7A_000205 Heterozygous; UV4 PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033233 Germline - 0/878 controls -MnlI;-KpnI;-NlaIV;-BanI;-Acc65I; - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+?/? 23 c.2904G>T r.(?) p.(Glu968Asp) - Parent #1 ACMG VUS g.76892635G>T g.77181589G>T - - MYO7A_000205 Heterozygous PubMed: Jacobson 2009; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033233 Germline - - -MnlI;-KpnI;-NlaIV;-BanI;-Acc65I; - - DNA SEQ - - USH1B ? PubMed: Jacobson 2009 Proband M - - - - - - - 1 William J. Kimberling
+?/? 23 c.2904G>T r.(?) p.(Glu968Asp) - Unknown ACMG VUS g.76892635G>T g.77181589G>T - - MYO7A_000205 Heterozygous PubMed: Bharadwaj 2000; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033233 Germline - 0/172 controls -MnlI;-KpnI;-NlaIV;-BanI;-Acc65I; - - DNA SEQ - - USH1B ? PubMed: Bharadwaj 2000 Proband - - Ireland - - - - - 1 Anne-Françoise Roux
+?/? 23 c.2904G>T r.(?) p.(Glu968Asp) - Unknown ACMG VUS g.76892635G>T g.77181589G>T - - MYO7A_000205 Heterozygous PubMed: Bharadwaj 2000; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033233 Germline - 0/172 controls -MnlI;-KpnI;-NlaIV;-BanI;-Acc65I; - - DNA SEQ - - USH1B ? PubMed: Bharadwaj 2000 Proband - - Ireland - - - - - 1 Anne-Françoise Roux
+?/? 23 c.2904G>T r.(?) p.(Glu968Asp) - Paternal (inferred) ACMG VUS g.76892635G>T g.77181589G>T - - MYO7A_000205 Homozygous PubMed: Ouyang 2005; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033233 Germline - - -MnlI;-KpnI;-NlaIV;-BanI;-Acc65I; - - DNA SEQ - - USH1B ? PubMed: Ouyang 2005 Proband - - United States - - - - - 1 Anne-Françoise Roux
+?/? 23 c.2904G>T r.(?) p.(Glu968Asp) - Maternal (inferred) ACMG VUS g.76892635G>T g.77181589G>T - - MYO7A_000205 Homozygous PubMed: Ouyang 2005; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033233 Germline - - -MnlI;-KpnI;-NlaIV;-BanI;-Acc65I; - - DNA SEQ - - USH1B ? PubMed: Ouyang 2005 Proband - - United States - - - - - 1 Anne-Françoise Roux
+?/. - c.2904G>T r.(?) p.(Glu968Asp) - Unknown - likely pathogenic g.76892635G>T g.77181589G>T MYO7A(NM_000260.4):c.2904G>T (p.E968D) - MYO7A_000205 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. 23 c.2904G>T r.(?) p.(Glu968Asp) - Parent #2 ACMG pathogenic (recessive) g.76892635G>T - - - MYO7A_000205 - PubMed: Bahena 2021 - - Germline yes - - - - DNA SEQ-NG-I - Exome sequencing USH1B Pat3 PubMed: Bahena 2021 - F no Iran - - - - - 1 Barbara Vona
+/. - c.2904G>T r.(?) p.(Glu968Asp) - Parent #1 - pathogenic g.76892635G>T g.77181589G>T - - MYO7A_000205 - PubMed: Neuhaus 2017 - rs111033233 Germline yes - - - - DNA SEQ - - USH Pat109 PubMed: Neuhaus 2017 - - no Germany;Iraq Persia - - - - 1 LOVD
+/. - c.2904G>T r.(?) p.(Glu968Asp) - Both (homozygous) - pathogenic g.76892635G>T g.77181589G>T - - MYO7A_000205 - PubMed: Neuhaus 2017 - rs111033233 Germline - - - - - DNA SEQ-NG - gene panel USH Pat130 PubMed: Neuhaus 2017 - - yes Syria - - - - - 1 LOVD
+/. - c.2904G>T r.(?) p.(Glu968Asp) - Parent #2 - pathogenic g.76892635G>T g.77181589G>T - - MYO7A_000205 - PubMed: Zhao 2015 - - Germline - - - - - DNA SEQ-NG - 86-gene panel retinal disease Rp41 PubMed: Zhao 2015 simplex case - - Northern Ireland - - - - - 1 LOVD
+?/. - c.2904G>T r.(?) p.(Glu968Asp) - Unknown - likely pathogenic g.76892635G>T - - - MYO7A_000205 - - - rs111033233 CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.2904G>T r.(?) p.(Glu968Asp) - Paternal (confirmed) ACMG likely pathogenic g.76892635G>T - - - MYO7A_000205 - PubMed: Mansard et al, 2021 - rs111033233 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - M - - - - - - - 1 Anne-Françoise Roux
+?/. 23 c.2904G>T r.(?) p.(Glu968Asp) - Parent #1 - likely pathogenic g.76892635G>T - c.2904G>T,p.E968D - MYO7A_000205 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease 1999(F-LMG353) PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
+/. 23 c.2904G>T r.(?) p.(Glu968Asp) - Parent #2 - pathogenic g.76892635G>T - c.2904G>T,p.E968D - MYO7A_000205 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease 2001(F-LMG353) PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
+/. 23 c.2904G>T r.(?) p.(Glu968Asp) - Parent #2 - pathogenic g.76892635G>T - c.2904G>T,p.E968D - MYO7A_000205 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease 2002(F-LMG353) PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
+/. - c.2904G>T r.(?) p.(Glu968Asp) - Unknown - pathogenic g.76892635G>T - MYO7A(NM_000260.4):c.2904G>T (p.E968D) - MYO7A_000205 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.