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.

10 entries on 1 page. Showing entries 1 - 10.
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     
+/+ 45 c.6070C>T r.(?) p.(Arg2024*) FERM 2 (1902-2205) Paternal (confirmed) - pathogenic g.76922215C>T g.77211170C>T - - MYO7A_000218 Heterozygous PubMed: Bonnet 2011 - rs111033198 Germline - - +DdeI;+BspCNI;-BsaJI; - - DNA SEQ - - USH1 - PubMed: Bonnet 2011 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 45 c.6070C>T r.(?) p.(Arg2024*) FERM 2 (1902-2205) Parent #2 - pathogenic g.76922215C>T g.77211170C>T - - MYO7A_000218 Heterozygous PubMed: Jacobson 2009 - rs111033198 Germline - - +DdeI;+BspCNI;-BsaJI; - - DNA SEQ - - USH1B ? PubMed: Jacobson 2009 Proband F - - - - - - - 1 William J. Kimberling
+/+ 45 c.6070C>T r.(?) p.(Arg2024*) FERM 2 (1902-2205) Paternal (confirmed) - pathogenic g.76922215C>T g.77211170C>T - - MYO7A_000218 Heterozygous PubMed: Le Quesne Stabej 2012 - rs111033198 Germline - - +DdeI;+BspCNI;-BsaJI; - - DNA SEQ - - USH1B ? PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/+ 45 c.6070C>T r.(?) p.(Arg2024*) FERM2 (1902-2205) Parent #2 - pathogenic g.76922215C>T g.77211170C>T - - MYO7A_000218 Heterozygous; mutation PubMed: Bonnet 2016 - rs111033198 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband - - Slovenia - - - - - 1 Crystel Bonnet
+/. - c.6070C>T r.(?) p.(Arg2024*) - Both (homozygous) - pathogenic (recessive) g.76922215C>T g.77211170C>T - - MYO7A_000218 - PubMed: Fuster-Garcia 2018 - - Germline - - - - - DNA arraySEQ - - retinal disease RP1580 PubMed: Fuster-Garcia 2018 analysis 77 USH patients - - Spain - - - - - 1 Global Variome, with Curator vacancy
+?/. - c.6070C>T r.(?) p.(Arg2024*) - Unknown - likely pathogenic g.76922215C>T g.77211170C>T c.223G>C p.(Asp75Hlis), c.6070C>T p.(Arg2024*) - MYO7A_000218 - PubMed: Hagag 2020 - - Germline/De novo (untested) ? - - - - DNA ? - - retinal disease Subject 030 PubMed: Hagag 2020 - ? - - - - - - - 1 LOVD
+?/. - c.6070C>T r.(?) p.(Arg2024*) - Parent #2 - likely pathogenic g.76922215C>T g.77211170C>T MYO7A c.6070C>T, p.R2024X - MYO7A_000218 compound heterozygous PubMed: Jauregui 2020 - - Unknown ? - - - - DNA SEQ-NG blood targeted sequencing retinal disease 141 PubMed: Jauregui 2020 - F - (United States) Hispanic - - - - 1 LOVD
+?/. 45 c.6070C>T r.(?) p.(Arg2024*) - Parent #2 - likely pathogenic (recessive) g.76922215C>T - c.6070C>T - MYO7A_000218 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease CIC06286 PubMed: Khateb 2020 simplex case F - - French - - - - 1 LOVD
+/. 45 c.6070C>T r.(?) p.(Arg2024*) - Unknown - pathogenic g.76922215C>T - c.6070C>T - MYO7A_000218 - PubMed: Cheng 2017 - - Germline yes - - - - DNA, RNA SEQ, PCR, SEQ-NG blood - retinal disease III:3 PubMed: Cheng 2017 Proband M ? China Chinese - - - - 1 LOVD
+/. 45 c.6070C>T r.(?) p.(Arg2024*) - Unknown - pathogenic g.76922215C>T - c.6070C>T - MYO7A_000218 - PubMed: Cheng 2017 - - Germline yes - - - - DNA, RNA SEQ, PCR, SEQ-NG blood - retinal disease III:4 PubMed: Cheng 2017 older brother of III:3 M ? China Chinese - - - - 1 LOVD
Legend   How to query  


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