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.

14 entries on 1 page. Showing entries 1 - 14.
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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     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/. 7 c.700C>T r.(?) p.(Gln234*) - Both (homozygous) - pathogenic g.76868015C>T g.77156969C>T - - MYO7A_000131 - Sharon, submitted - - Germline - - - - - DNA SEQ - - USH1 - Sharon, submitted - F yes Israel Arab-Muslim - - - - 3 Dror Sharon
+/+ 7 c.700C>T r.(?) p.(Gln234*) Motor domain (1-729) Parent #2 - pathogenic g.76868015C>T g.77156969C>T - - MYO7A_000131 Heterozygous PubMed: Levy 1997 - rs41298133 Germline - - -MwoI;-AlwNI;-BstAPI; - - DNA SEQ - - USH1B ? PubMed: Levy 1997 Proband - - - - - - - - 1 Anne-Françoise Roux
+/+ 7 c.700C>T r.(?) p.(Gln234*) Motor domain (1-729) Maternal (confirmed) - pathogenic g.76868015C>T g.77156969C>T - - MYO7A_000131 Heterozygous PubMed: Roux 2011 - rs41298133 Germline - - -MwoI;-AlwNI;-BstAPI; - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband M - France - - - - - 1 Anne-Françoise Roux
+/+ 7 c.700C>T r.(?) p.(Gln234*) Motor domain (1-729) Paternal (inferred) - pathogenic g.76868015C>T g.77156969C>T - - MYO7A_000131 Homozygous PubMed: Rizel 2012 - rs41298133 Germline - - -MwoI;-AlwNI;-BstAPI; - - DNA SEQ - - USH1B ? PubMed: Rizel 2012 Proband M - Israel - - - - - 1 Anne-Françoise Roux
+/+ 7 c.700C>T r.(?) p.(Gln234*) Motor domain (1-729) Maternal (inferred) - pathogenic g.76868015C>T g.77156969C>T - - MYO7A_000131 Homozygous PubMed: Rizel 2012 - rs41298133 Germline - - -MwoI;-AlwNI;-BstAPI; - - DNA SEQ - - USH1B ? PubMed: Rizel 2012 Proband M - Israel - - - - - 1 Anne-Françoise Roux
+/+ 7 c.700C>T r.(?) p.(Gln234*) Motor domain (1-729) Maternal (confirmed) - pathogenic g.76868015C>T g.77156969C>T - - MYO7A_000131 Homozygous; mutation PubMed: Bonnet 2016 - rs41298133 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband F - France - - - - - 1 Crystel Bonnet
+/+ 7 c.700C>T r.(?) p.(Gln234*) Motor domain (1-729) Paternal (confirmed) - pathogenic g.76868015C>T g.77156969C>T - - MYO7A_000131 Homozygous; mutation PubMed: Bonnet 2016 - rs41298133 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband F - France - - - - - 1 Crystel Bonnet
+/. - c.700C>T r.(?) p.(Gln234*) - Unknown ACMG pathogenic g.76868015C>T - - - MYO7A_000131 - PubMed: Sharon 2019 - - Germline - 5/2420 IRD families - - - DNA SEQ - - retinal disease - PubMed: Sharon 2019 5 IRD families - - Israel - - - - - 5 Global Variome, with Curator vacancy
+/. - c.700C>T r.(?) p.(Gln234Ter) - Both (homozygous) ACMG pathogenic g.76868015C>T - - - MYO7A_000131 - PubMed: Mansard et al, 2021 - rs41298133 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
+/. - c.700C>T r.(?) p.(Gln234Ter) - Both (homozygous) ACMG pathogenic g.76868015C>T - - - MYO7A_000131 - PubMed: Mansard et al, 2021 - rs41298133 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
?/. 7 c.700C>T r.(?) p.(Gln234*) - Unknown - VUS g.76868015C>T - c.700C>T - MYO7A_000131 - PubMed: Khalaileh-2018 - - Unknown - - - - - DNA PCR, SEQ blood - retinal disease - PubMed: Khalaileh-2018 - - yes - Arab Muslim - - - - 1 LOVD
?/. 7 c.700C>T r.(?) p.(Gln234*) - Unknown - VUS g.76868015C>T - c.700C>T - MYO7A_000131 - PubMed: Khalaileh-2018 - - Unknown - - - - - DNA PCR, SEQ blood - retinal disease - PubMed: Khalaileh-2018 - - yes - Arab Muslim - - - - 1 LOVD
?/. 7 c.700C>T r.(?) p.(Gln234*) - Unknown - VUS g.76868015C>T - c.700C>T - MYO7A_000131 - PubMed: Khalaileh-2018 - - Unknown - - - - - DNA PCR, SEQ blood - retinal disease - PubMed: Khalaileh-2018 - - yes - Arab Muslim - - - - 1 LOVD
?/. 7 c.700C>T r.(?) p.(Gln234*) - Unknown - VUS g.76868015C>T - c.700C>T - MYO7A_000131 - PubMed: Khalaileh-2018 - - Unknown - - - - - DNA PCR, SEQ blood - retinal disease - PubMed: Khalaileh-2018 - - yes - Arab Muslim - - - - 1 LOVD
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