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.

5 entries on 1 page. Showing entries 1 - 5.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

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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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Re-site     

VIP     

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Disease     

ID_report     

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Remarks     

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VIP     

Data_av     

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Owner     
-/. - c.2035G>A r.(?) p.(Val679Ile) - Unknown - benign g.76885901G>A g.77174855G>A - - MYO7A_000066 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/- 17 c.2035G>A r.(?) p.(Val679Ile) Motor domain (1-729) Paternal (inferred) - benign g.76885901G>A g.77174855G>A - - MYO7A_000066 Homozygous PubMed: Roux 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs35641839 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Roux 2006 Proband M - Morocco - - - - - 1 Anne-Françoise Roux
-/- 17 c.2035G>A r.(?) p.(Val679Ile) Motor domain (1-729) Maternal (inferred) - benign g.76885901G>A g.77174855G>A - - MYO7A_000066 Homozygous PubMed: Roux 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs35641839 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Roux 2006 Proband M - Morocco - - - - - 1 Anne-Françoise Roux
-/- 17 c.2035G>A r.(?) p.(Val679Ile) Motor domain (1-729) Paternal (inferred) - benign g.76885901G>A g.77174855G>A - - MYO7A_000066 Homozygous PubMed: Roux 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs35641839 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Roux 2006 Proband M - Senegal - - - - - 1 Anne-Françoise Roux
-/- 17 c.2035G>A r.(?) p.(Val679Ile) Motor domain (1-729) Maternal (inferred) - benign g.76885901G>A g.77174855G>A - - MYO7A_000066 Homozygous PubMed: Roux 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs35641839 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Roux 2006 Proband M - Senegal - - - - - 1 Anne-Françoise Roux
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