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     
+/+ 14 c.1623dup r.(?) p.(Lys542Glnfs*5) Motor domain (1-729) Maternal (inferred) - pathogenic g.76873967dup g.77162921dup - - MYO7A_000227 Homozygous; possible pathogenic PubMed: Yoshimura 2014 - - Germline - - none - - DNA SEQ - - USH1 - PubMed: Yoshimura 2014 Proband - - Japan - - - - - 1 Anne-Françoise Roux
+/+ 14 c.1623dup r.(?) p.(Lys542Glnfs*5) Motor domain (1-729) Paternal (inferred) - pathogenic g.76873967dup g.77162921dup - - MYO7A_000227 Homozygous; possible pathogenic PubMed: Yoshimura 2014 - - Germline - - none - - DNA SEQ - - USH1 - PubMed: Yoshimura 2014 Proband - - Japan - - - - - 1 Anne-Françoise Roux
+/+ 14 c.1623dup r.(?) p.(Lys542Glnfs*5) Motor domain (1-729) Unknown - pathogenic g.76873967dup g.77162921dup - - MYO7A_000227 Heterozygous PubMed: Le Quesne Stabej 2012 - - Germline - - none - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/+ 14 c.1623dup r.(?) p.(Lys542Glnfs*5) Motor domain (1-729) Maternal (confirmed) - pathogenic g.76873967dup g.77162921dup - - MYO7A_000227 Heterozygous PubMed: Le Quesne Stabej 2012 - - Germline - - none - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/+ 14 c.1623dup r.(?) p.(Lys542Glnfs*5) Motor domain (1-729) Paternal (inferred) - pathogenic g.76873967dup g.77162921dup - - MYO7A_000227 Homozygous PubMed: Bharadwaj 2000 - - Germline - - none - - DNA SEQ - - USH1B ? PubMed: Bharadwaj 2000 Proband - - Italy - - - - - 1 Anne-Françoise Roux
+/+ 14 c.1623dup r.(?) p.(Lys542Glnfs*5) Motor domain (1-729) Maternal (inferred) - pathogenic g.76873967dup g.77162921dup - - MYO7A_000227 Homozygous PubMed: Bharadwaj 2000 - - Germline - - none - - DNA SEQ - - USH1B ? PubMed: Bharadwaj 2000 Proband - - Italy - - - - - 1 Anne-Françoise Roux
+/+ 14 c.1623dup r.(?) p.(Lys542Glnfs*5) Motor domain (1-729) Unknown - pathogenic g.76873967dup g.77162921dup - - MYO7A_000227 Heterozygous PubMed: Bharadwaj 2000 - - Germline - - none - - DNA SEQ - - USH1B ? PubMed: Bharadwaj 2000 Proband - - Ireland - - - - - 1 Anne-Françoise Roux
+/. - c.1623dup r.(?) p.(Lys542Glnfs*5) - Parent #1 - pathogenic (recessive) g.76873967dup g.77162921dup c.1623dupC - MYO7A_000227 - PubMed: Fuster-Garcia 2018 - - Germline - - - - - DNA arraySEQ - - retinal disease RP1768t PubMed: Fuster-Garcia 2018 analysis 77 USH patients - - Spain - - - - - 1 Global Variome, with Curator vacancy
+?/. - c.1623dup r.(?) p.(Lys542Glnfs*5) - Parent #2 - likely pathogenic g.76873967dup g.77162921dup 1616_1617insC - MYO7A_000227 - PubMed: Stone 2017 - - Germline - - - - - DNA SEQ-NG - - retinal disease 526 PubMed: Stone 2017 1 affected M - (United States) - - - - - 1 LOVD
+?/. - c.1623dup r.(?) p.(Lys542Glnfs*5) - Unknown - likely pathogenic g.76873967dup g.77162921dup MYO7A;NM_000260.3;c.[1623dup];[1623=];p.[(Lys542Glnfs*5)];[=];No relevant CNV detected - MYO7A_000227 single heterozygous variant in a recessive disease PubMed: Jiman 2020 - - Unknown ? - - - - DNA SEQ-NG-I - 176 genes panel retinal disease 27 PubMed: Jiman 2020 - F - (United Kingdom (Great Britain)) - - - - - 1 LOVD
+/. 14 c.1623dup r.(?) p.(Lys542Glnfs*5) - Parent #1 - pathogenic g.76873967dup - c.1623dupC - MYO7A_000227 - PubMed: Galbis-Martinez-2021 - - Germline - - - - - DNA ? - - retinal disease - PubMed: Galbis-Martinez-2021 - - - - - - - - - 4 LOVD
+/. - c.1623dupC r.(?) p.(Lys542GlnfsTer5) - Unknown ACMG pathogenic g.76873967dup - - - MYO7A_000227 - PubMed: Mansard et al, 2021 - rs782077721 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
Legend   How to query  


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