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.

6 entries on 1 page. Showing entries 1 - 6.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

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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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Disease     

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Owner     
-/. - c.4589C>T r.(?) p.(Ser1530Leu) - Unknown - benign g.76910600C>T g.77199555C>T - - MYO7A_000069 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/- 35 c.4589C>T r.(?) p.(Ser1530Leu) FERM 1 (1258-1602) Paternal (inferred) - benign g.76910600C>T g.77199555C>T - - MYO7A_000069 Homozygous PubMed: Roux 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033183 Germline - - -TspRI - - DNA SEQ - - USH1B ? PubMed: Roux 2006 Proband M - Morocco - - - - - 1 Anne-Françoise Roux
-/- 35 c.4589C>T r.(?) p.(Ser1530Leu) FERM 1 (1258-1602) Maternal (inferred) - benign g.76910600C>T g.77199555C>T - - MYO7A_000069 Homozygous PubMed: Roux 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033183 Germline - - -TspRI - - DNA SEQ - - USH1B ? PubMed: Roux 2006 Proband M - Morocco - - - - - 1 Anne-Françoise Roux
-/- 35 c.4589C>T r.(?) p.(Ser1530Leu) FERM 1 (1258-1602) Paternal (inferred) - benign g.76910600C>T g.77199555C>T - - MYO7A_000069 Homozygous PubMed: Roux 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033183 Germline - - -TspRI - - DNA SEQ - - USH1B ? PubMed: Roux 2006 Proband M - Senegal - - - - - 1 Anne-Françoise Roux
-/- 35 c.4589C>T r.(?) p.(Ser1530Leu) FERM 1 (1258-1602) Maternal (inferred) - benign g.76910600C>T g.77199555C>T - - MYO7A_000069 Homozygous PubMed: Roux 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033183 Germline - - -TspRI - - DNA SEQ - - USH1B ? PubMed: Roux 2006 Proband M - Senegal - - - - - 1 Anne-Françoise Roux
-/- 35 c.4589C>T r.(?) p.(Ser1530Leu) FERM 1 (1258-1602) Paternal (inferred) - benign g.76910600C>T g.77199555C>T - - MYO7A_000069 Homozygous; predicted benign PubMed: Neveling 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033183 Germline - - -TspRI - - DNA SEQ, SEQ-NG-S - - RPar ? PubMed: Neveling 2012 Proband M - - - - - - - 1 Anne-Françoise Roux
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