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)     

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ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

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Re-site     

VIP     

Methylation     

Template     

Technique     

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Disease     

ID_report     

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Owner     
-/. - c.5866G>A r.(?) p.(Val1956Ile) - Unknown - benign g.76919484G>A g.77208439G>A MYO7A(NM_000260.3):c.5866G>A (p.V1956I, p.(Val1956Ile)), MYO7A(NM_000260.4):c.5866G>A (p.V1956I) - MYO7A_000376 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.5866G>A r.(?) p.(Val1956Ile) - Unknown - likely benign g.76919484G>A g.77208439G>A MYO7A(NM_000260.3):c.5866G>A (p.V1956I, p.(Val1956Ile)), MYO7A(NM_000260.4):c.5866G>A (p.V1956I) - MYO7A_000376 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/. - c.5866G>A r.(?) p.(Val1956Ile) - Unknown - benign g.76919484G>A g.77208439G>A MYO7A(NM_000260.3):c.5866G>A (p.V1956I, p.(Val1956Ile)), MYO7A(NM_000260.4):c.5866G>A (p.V1956I) - MYO7A_000376 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/- 43 c.5866G>A r.(?) p.(Val1956Ile) FERM 2 (1902-2205) Unknown - benign g.76919484G>A g.77208439G>A - - MYO7A_000376 Heterozygous; UV1 PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs142293185 Germline - 2/846 controls +BsmI - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/- 43 c.5866G>A r.(?) p.(Val1956Ile) FERM 2 (1902-2205) Unknown - benign g.76919484G>A g.77208439G>A - - MYO7A_000376 Heterozygous; UV1 PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs142293185 Germline - 2/846 controls +BsmI - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/- 43 c.5866G>A r.(?) p.(Val1956Ile) FERM 2 (1902-2205) Unknown - benign g.76919484G>A g.77208439G>A - - MYO7A_000376 Heterozygous; UV1 PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs142293185 Germline - 2/844 controls +BsmI - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/- 43 c.5866G>A r.(?) p.(Val1956Ile) FERM 2 (1902-2205) Parent #1 - benign g.76919484G>A g.77208439G>A - - MYO7A_000376 Heterozygous; UV1 PubMed: Sodi 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs142293185 Germline - - +BsmI - - DNA SEQ - - USH2 ? PubMed: Sodi 2014 Proband - - Italy - - - - - 1 Anne-Françoise Roux
-?/. - c.5866G>A r.(?) p.(Val1956Ile) - Unknown - likely benign g.76919484G>A g.77208439G>A MYO7A(NM_000260.3):c.5866G>A (p.V1956I, p.(Val1956Ile)), MYO7A(NM_000260.4):c.5866G>A (p.V1956I) - MYO7A_000376 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.5866G>A r.(?) p.(Val1956Ile) - Both (homozygous) - likely benign g.76919484G>A g.77208439G>A - - MYO7A_000376 1 homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs142293185 Germline - 1/2795 individuals - - - DNA arraySNP - Infinium Global Screening Array v1.0 ? - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - 1 Mohammed Faruq
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