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     
+/+ 17 c.1996C>T r.(?) p.(Arg666*) Motor domain (1-729) Parent #1 - pathogenic g.76885862C>T g.77174816C>T - - MYO7A_000154 Heterozygous PubMed: Pennings 2004 - rs121965085 Germline - - -BtsCI;-FokI; - - DNA SEQ - - USH1B ? PubMed: Pennings 2004 Proband - - Netherlands - - - - - 1 Anne-Françoise Roux
+/+ 17 c.1996C>T r.(?) p.(Arg666*) Motor domain (1-729) Parent #1 - pathogenic g.76885862C>T g.77174816C>T - - MYO7A_000154 Heterozygous PubMed: Ouyang 2005 - rs121965085 Germline - - -BtsCI;-FokI; - - DNA SEQ - - USH1B ? PubMed: Ouyang 2005 Proband - - United Kingdom (Great Britain) - - - - - 1 Anne-Françoise Roux
+/+ 17 c.1996C>T r.(?) p.(Arg666*) Motor domain (1-729) Unknown - pathogenic g.76885862C>T g.77174816C>T - - MYO7A_000154 Heterozygous PubMed: Ouyang 2005 - rs121965085 Germline - - -BtsCI;-FokI; - - DNA SEQ - - USH1B ? PubMed: Ouyang 2005 Proband - - United Kingdom (Great Britain) - - - - - 1 Anne-Françoise Roux
+/+ 17 c.1996C>T r.(?) p.(Arg666*) Motor domain (1-729) Unknown - pathogenic g.76885862C>T g.77174816C>T - - MYO7A_000154 Heterozygous PubMed: Ouyang 2005 - rs121965085 Germline - - -BtsCI;-FokI; - - DNA SEQ - - USH1B ? PubMed: Ouyang 2005 Proband - - United Kingdom (Great Britain) - - - - - 1 Anne-Françoise Roux
+/+ 17 c.1996C>T r.(?) p.(Arg666*) Motor domain (1-729) Unknown - pathogenic g.76885862C>T g.77174816C>T - - MYO7A_000154 Heterozygous PubMed: Ouyang 2005 - rs121965085 Germline - - -BtsCI;-FokI; - - DNA SEQ - - USH1B ? PubMed: Ouyang 2005 Proband - - United Kingdom (Great Britain) - - - - - 1 Anne-Françoise Roux
+/+ 17 c.1996C>T r.(?) p.(Arg666*) Motor domain (1-729) Unknown - pathogenic g.76885862C>T g.77174816C>T - - MYO7A_000154 Heterozygous PubMed: Ouyang 2005 - rs121965085 Germline - - -BtsCI;-FokI; - - DNA SEQ - - USH1B ? PubMed: Ouyang 2005 Proband - - United Kingdom (Great Britain) - - - - - 1 Anne-Françoise Roux
+/+ 17 c.1996C>T r.(?) p.(Arg666*) Motor domain (1-729) Parent #2 - pathogenic g.76885862C>T g.77174816C>T - - MYO7A_000154 Heterozygous PubMed: Janecke 1999, PubMed: Dad 2016 - rs121965085 Germline - - -BtsCI;-FokI; - - DNA SEQ - - USH1B ? PubMed: Janecke 1999, PubMed: Dad 2016 Proband - - - - - - - - 1 Anne-Françoise Roux
+/+ 17 c.1996C>T r.(?) p.(Arg666*) Motor domain (1-729) Parent #1 - pathogenic g.76885862C>T g.77174816C>T - - MYO7A_000154 Heterozygous PubMed: Bonnet 2011 - rs121965085 Germline - - -BtsCI;-FokI; - - DNA SEQ - - USH1B ? PubMed: Bonnet 2011 Proband - - - - - - - - 1 Anne-Françoise Roux
+/+ 17 c.1996C>T r.(?) p.(Arg666*) Motor domain (1-729) Unknown - pathogenic g.76885862C>T g.77174816C>T - - MYO7A_000154 Heterozygous; mutation PubMed: Bonnet 2016 - rs121965085 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband - - Germany - - - - - 1 Crystel Bonnet
+/+ 17 c.1996C>T r.(?) p.(Arg666*) Motor domain (1-729) Parent #1 - pathogenic g.76885862C>T g.77174816C>T - - MYO7A_000154 Heterozygous; mutation PubMed: Bonnet 2016 - rs121965085 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband - - Slovenia - - - - - 1 Crystel Bonnet
+/. - c.1996C>T r.(?) p.(Arg666Ter) - Unknown - pathogenic g.76885862C>T g.77174816C>T MYO7A(NM_000260.3):c.1996C>T (p.R666*) - MYO7A_000154 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.1996C>T r.(?) p.(Arg666*) - Parent #1 - likely pathogenic g.76885862C>T g.77174816C>T MYO7A, variant 1: c.1996C>T/p.R666*, variant 2: c.3503G>A/p.R1168Q - MYO7A_000154 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET8 targeted sequencing panel - see paper retinal disease 126 PubMed: Weisschuh 2020 Filing key number: 56, Usher syndrome type I, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
+/. 17 c.1996C>T r.(?) p.(Arg666*) - Both (homozygous) - pathogenic g.76885862C>T - c.1996C>T - MYO7A_000154 - PubMed: Galbis-Martinez-2021 - - Germline - - - - - DNA ? - - retinal disease - PubMed: Galbis-Martinez-2021 - - - - - - - - - 4 LOVD
+/. 17 c.1996C>T r.(?) p.(Arg666*) - Parent #2 - pathogenic g.76885862C>T - c.1996C>T - MYO7A_000154 - PubMed: Galbis-Martinez-2021 - - Germline - - - - - DNA ? - - retinal disease - PubMed: Galbis-Martinez-2021 - - - - - - - - - 4 LOVD
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