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.

9 entries on 1 page. Showing entries 1 - 9.
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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     

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Remarks     

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VIP     

Data_av     

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Panel size     

Owner     
-/. - c.5619G>A r.(?) p.(Arg1873=) - Unknown - benign g.76916645G>A g.77205600G>A - - MYO7A_000392 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/- 40 c.5619G>A r.(?) p.(=) MyTH4 2 (1747-1896) Paternal (inferred) - benign g.76916645G>A g.77205600G>A - - MYO7A_000392 Homozygous; UV1 PubMed: Le Quesne Stabej 2012 - rs45450893 Germline - 0/96 controls +MlyI;+PleI;+HinfI;-BceAI;-NlaIV;-CviKI_1; - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/- 40 c.5619G>A r.(?) p.(=) MyTH4 2 (1747-1896) Maternal (inferred) - benign g.76916645G>A g.77205600G>A - - MYO7A_000392 Homozygous; UV1 PubMed: Le Quesne Stabej 2012 - rs45450893 Germline - 0/96 controls +MlyI;+PleI;+HinfI;-BceAI;-NlaIV;-CviKI_1; - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/- 40 c.5619G>A r.(?) p.(=) MyTH4 2 (1747-1896) Maternal (inferred) - benign g.76916645G>A g.77205600G>A - - MYO7A_000392 Homozygous; UV1 PubMed: Le Quesne Stabej 2012 - rs45450893 Germline - 0/96 controls +MlyI;+PleI;+HinfI;-BceAI;-NlaIV;-CviKI_1; - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/- 40 c.5619G>A r.(?) p.(=) MyTH4 2 (1747-1896) Paternal (inferred) - benign g.76916645G>A g.77205600G>A - - MYO7A_000392 Homozygous; UV1 PubMed: Le Quesne Stabej 2012 - rs45450893 Germline - 0/96 controls +MlyI;+PleI;+HinfI;-BceAI;-NlaIV;-CviKI_1; - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/- 40 c.5619G>A r.(?) p.(=) MyTH4 2 (1747-1896) Unknown - benign g.76916645G>A g.77205600G>A - - MYO7A_000392 Heterozygous; UV1 PubMed: Le Quesne Stabej 2012 - rs45450893 Germline - 0/96 controls +MlyI;+PleI;+HinfI;-BceAI;-NlaIV;-CviKI_1; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/- 40 c.5619G>A r.(?) p.(=) MyTH4 2 (1747-1896) Unknown - benign g.76916645G>A g.77205600G>A - - MYO7A_000392 Heterozygous; UV1 PubMed: Le Quesne Stabej 2012 - rs45450893 Germline - 0/96 controls +MlyI;+PleI;+HinfI;-BceAI;-NlaIV;-CviKI_1; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/- 40 c.5619G>A r.(?) p.(=) MyTH4 2 (1747-1896) Unknown - benign g.76916645G>A g.77205600G>A - - MYO7A_000392 Heterozygous; UV1 PubMed: Le Quesne Stabej 2012 - rs45450893 Germline - 0/96 controls +MlyI;+PleI;+HinfI;-BceAI;-NlaIV;-CviKI_1; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-?/. - c.5619G>A r.(=) p.(=) - Parent #1 - likely benign g.76916645G>A g.77205600G>A - - MYO7A_000392 9 heterozygous, no homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs45450893 Germline - 9/2795 individuals - - - DNA arraySNP - Infinium Global Screening Array v1.0 ? - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - 9 Mohammed Faruq
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