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.

16 entries on 1 page. Showing entries 1 - 16.
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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     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
-/- 39i c.5481-83A>G r.(=) p.(=) - Paternal (inferred) - benign g.76916424A>G g.77205379A>G - - MYO7A_000084 Homozygous PubMed: Blanchet 2007 - rs11237121 Germline - - +HpyCH4IV;+BsaAI;-FatI;-NlaIII;-CviAII; - - DNA SEQ - - USH1B ? PubMed: Blanchet 2007 Proband M - France - - - - - 1 Anne-Françoise Roux
-/- 39i c.5481-83A>G r.(=) p.(=) - Maternal (inferred) - benign g.76916424A>G g.77205379A>G - - MYO7A_000084 Homozygous PubMed: Blanchet 2007 - rs11237121 Germline - - +HpyCH4IV;+BsaAI;-FatI;-NlaIII;-CviAII; - - DNA SEQ - - USH1B ? PubMed: Blanchet 2007 Proband M - France - - - - - 1 Anne-Françoise Roux
-/- 39i c.5481-83A>G r.(=) p.(=) - Paternal (inferred) - benign g.76916424A>G g.77205379A>G - - MYO7A_000084 Homozygous PubMed: Roux 2011 - rs11237121 Germline - - +HpyCH4IV;+BsaAI;-FatI;-NlaIII;-CviAII; - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband F - France - - - - - 1 Anne-Françoise Roux
-/- 39i c.5481-83A>G r.(=) p.(=) - Maternal (inferred) - benign g.76916424A>G g.77205379A>G - - MYO7A_000084 Homozygous PubMed: Roux 2011 - rs11237121 Germline - - +HpyCH4IV;+BsaAI;-FatI;-NlaIII;-CviAII; - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband F - France - - - - - 1 Anne-Françoise Roux
-/- 39i c.5481-83A>G r.(=) p.(=) - Paternal (inferred) - benign g.76916424A>G g.77205379A>G - - MYO7A_000084 Homozygous PubMed: Roux 2011 - rs11237121 Germline - - +HpyCH4IV;+BsaAI;-FatI;-NlaIII;-CviAII; - - DNA minigene, SEQ - - USH1B ? PubMed: Roux 2011 Proband M - France - - - - - 1 Anne-Françoise Roux
-/- 39i c.5481-83A>G r.(=) p.(=) - Maternal (inferred) - benign g.76916424A>G g.77205379A>G - - MYO7A_000084 Homozygous PubMed: Roux 2011 - rs11237121 Germline - - +HpyCH4IV;+BsaAI;-FatI;-NlaIII;-CviAII; - - DNA minigene, SEQ - - USH1B ? PubMed: Roux 2011 Proband M - France - - - - - 1 Anne-Françoise Roux
-/- 39i c.5481-83A>G r.(=) p.(=) - Unknown - benign g.76916424A>G g.77205379A>G - - MYO7A_000084 Heterozygous PubMed: Roux 2011 - rs11237121 Germline - - +HpyCH4IV;+BsaAI;-FatI;-NlaIII;-CviAII; - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband M - France - - - - - 1 Anne-Françoise Roux
-/- 39i c.5481-83A>G r.(=) p.(=) - Unknown - benign g.76916424A>G g.77205379A>G - - MYO7A_000084 Heterozygous PubMed: Roux 2011 - rs11237121 Germline - - +HpyCH4IV;+BsaAI;-FatI;-NlaIII;-CviAII; - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband M - - - - - - - 1 Anne-Françoise Roux
-/- 39i c.5481-83A>G r.(=) p.(=) - Paternal (inferred) - benign g.76916424A>G g.77205379A>G - - MYO7A_000084 Homozygous PubMed: Roux 2011 - rs11237121 Germline - - +HpyCH4IV;+BsaAI;-FatI;-NlaIII;-CviAII; - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband F - Italy - - - - - 1 Anne-Françoise Roux
-/- 39i c.5481-83A>G r.(=) p.(=) - Maternal (inferred) - benign g.76916424A>G g.77205379A>G - - MYO7A_000084 Homozygous PubMed: Roux 2011 - rs11237121 Germline - - +HpyCH4IV;+BsaAI;-FatI;-NlaIII;-CviAII; - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband F - Italy - - - - - 1 Anne-Françoise Roux
-/- 39i c.5481-83A>G r.(=) p.(=) - Paternal (inferred) - benign g.76916424A>G g.77205379A>G - - MYO7A_000084 Homozygous PubMed: Roux 2011 - rs11237121 Germline - - +HpyCH4IV;+BsaAI;-FatI;-NlaIII;-CviAII; - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband M - France - - - - - 1 Anne-Françoise Roux
-/- 39i c.5481-83A>G r.(=) p.(=) - Maternal (inferred) - benign g.76916424A>G g.77205379A>G - - MYO7A_000084 Homozygous PubMed: Roux 2011 - rs11237121 Germline - - +HpyCH4IV;+BsaAI;-FatI;-NlaIII;-CviAII; - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband M - France - - - - - 1 Anne-Françoise Roux
-/- 39i c.5481-83A>G r.(=) p.(=) - Unknown - benign g.76916424A>G g.77205379A>G - - MYO7A_000084 Heterozygous PubMed: Roux 2011 - rs11237121 Germline - - +HpyCH4IV;+BsaAI;-FatI;-NlaIII;-CviAII; - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband F - France - - - - - 1 Anne-Françoise Roux
-/- 39i c.5481-83A>G r.(=) p.(=) - Unknown - benign g.76916424A>G g.77205379A>G - - MYO7A_000084 Heterozygous - - rs11237121 Germline - - +HpyCH4IV;+BsaAI;-FatI;-NlaIII;-CviAII; - - DNA SEQ - - USH1B ? PubMed: Besnard, Garcia-Garcia 2014 Proband M - France - - - - - 1 Anne-Françoise Roux
-/- 39i c.5481-83A>G r.(=) p.(=) - Paternal (inferred) - benign g.76916424A>G g.77205379A>G - - MYO7A_000084 Homozygous PubMed: Roux 2011 - rs11237121 Germline - - +HpyCH4IV;+BsaAI;-FatI;-NlaIII;-CviAII; - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband M - - - - - - - 1 Anne-Françoise Roux
-/- 39i c.5481-83A>G r.(=) p.(=) - Maternal (inferred) - benign g.76916424A>G g.77205379A>G - - MYO7A_000084 Homozygous PubMed: Roux 2011 - rs11237121 Germline - - +HpyCH4IV;+BsaAI;-FatI;-NlaIII;-CviAII; - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband M - - - - - - - 1 Anne-Françoise Roux
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