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.

21 entries on 1 page. Showing entries 1 - 21.
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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     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
-/- 37 c.5156A>G r.(?) p.(Tyr1719Cys) - Unknown - benign g.76913457A>G g.77202412A>G - - MYO7A_000081 Heterozygous; Neutral PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs77625410 Germline - 9/864 controls +Tsp45I - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/- 37 c.5156A>G r.(?) p.(Tyr1719Cys) - Unknown - benign g.76913457A>G g.77202412A>G - - MYO7A_000081 Heterozygous; Neutral PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs77625410 Germline - 9/864 controls +Tsp45I - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/- 37 c.5156A>G r.(?) p.(Tyr1719Cys) - Paternal (confirmed) - benign g.76913457A>G g.77202412A>G - - MYO7A_000081 Heterozygous; Neutral PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs77625410 Germline - 9/864 controls +Tsp45I - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/- 37 c.5156A>G r.(?) p.(Tyr1719Cys) - Unknown - benign g.76913457A>G g.77202412A>G - - MYO7A_000081 Heterozygous; Neutral PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs77625410 Germline - 9/864 controls +Tsp45I - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/- 37 c.5156A>G r.(?) p.(Tyr1719Cys) - Unknown - benign g.76913457A>G g.77202412A>G - - MYO7A_000081 Heterozygous; Neutral PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs77625410 Germline - 9/864 controls +Tsp45I - - DNA SEQ - - USH - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/- 37 c.5156A>G r.(?) p.(Tyr1719Cys) - Unknown - benign g.76913457A>G g.77202412A>G - - MYO7A_000081 Heterozygous; Neutral PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs77625410 Germline - 9/864 controls +Tsp45I - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/- 37 c.5156A>G r.(?) p.(Tyr1719Cys) - Parent #2 - benign g.76913457A>G g.77202412A>G - - MYO7A_000081 Heterozygous PubMed: Roux 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs77625410 Germline - 8/1104 controls +Tsp45I - - DNA SEQ - - USH1B ? PubMed: Roux 2006 Proband F - France - - - - - 1 Anne-Françoise Roux
-/- 37 c.5156A>G r.(?) p.(Tyr1719Cys) - Unknown - benign g.76913457A>G g.77202412A>G - - MYO7A_000081 Heterozygous PubMed: Blanchet 2007; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs77625410 Germline - - +Tsp45I - - DNA SEQ - - USH1B ? PubMed: Blanchet 2007 Proband M - France - - - - - 1 Anne-Françoise Roux
-/- 37 c.5156A>G r.(?) p.(Tyr1719Cys) - Unknown - benign g.76913457A>G g.77202412A>G - - MYO7A_000081 Heterozygous PubMed: Roux 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs77625410 Germline - - +Tsp45I - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband M - - north Africa - - - - 1 Anne-Françoise Roux
-/- 37 c.5156A>G r.(?) p.(Tyr1719Cys) - Unknown - benign g.76913457A>G g.77202412A>G - - MYO7A_000081 Heterozygous PubMed: Roux 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs77625410 Germline - - +Tsp45I - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband F - France - - - - - 1 Anne-Françoise Roux
-/- 37 c.5156A>G r.(?) p.(Tyr1719Cys) - Paternal (inferred) - benign g.76913457A>G g.77202412A>G - - MYO7A_000081 Homozygous PubMed: Boulouiz 2007; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs77625410 Germline - 15/226 controls +Tsp45I - - DNA SEQ - - USH1B ? PubMed: Boulouiz 2007 Proband F - Morocco - - - - - 1 Anne-Françoise Roux
-/- 37 c.5156A>G r.(?) p.(Tyr1719Cys) - Maternal (inferred) - benign g.76913457A>G g.77202412A>G - - MYO7A_000081 Homozygous PubMed: Boulouiz 2007; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs77625410 Germline - 15/226 controls +Tsp45I - - DNA SEQ - - USH1B ? PubMed: Boulouiz 2007 Proband F - Morocco - - - - - 1 Anne-Françoise Roux
-/- 37 c.5156A>G r.(?) p.(Tyr1719Cys) - Paternal (inferred) - benign g.76913457A>G g.77202412A>G - - MYO7A_000081 Homozygous PubMed: Boulouiz 2007; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs77625410 Germline - 15/226 controls +Tsp45I - - DNA SEQ - - USH1B ? PubMed: Boulouiz 2007 Relative F - Morocco - - - - - 1 Anne-Françoise Roux
-/- 37 c.5156A>G r.(?) p.(Tyr1719Cys) - Maternal (inferred) - benign g.76913457A>G g.77202412A>G - - MYO7A_000081 Homozygous PubMed: Boulouiz 2007; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs77625410 Germline - 15/226 controls +Tsp45I - - DNA SEQ - - USH1B ? PubMed: Boulouiz 2007 Relative F - Morocco - - - - - 1 Anne-Françoise Roux
-/- 37 c.5156A>G r.(?) p.(Tyr1719Cys) - Parent #2 - benign g.76913457A>G g.77202412A>G - - MYO7A_000081 Heterozygous PubMed: Cuevas 1999; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs77625410 Germline - 0/68 controls +Tsp45I - - DNA SEQ - - USH1B ? PubMed: Cuevas 1999 Proband M - Spain - - - - - 1 Jose Maria Millan
-/- 37 c.5156A>G r.(?) p.(Tyr1719Cys) - Parent #1 - benign g.76913457A>G g.77202412A>G - - MYO7A_000081 Heterozygous PubMed: Cuevas 1999; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs77625410 Germline - 0/68 controls +Tsp45I - - DNA SEQ - - USH1B ? PubMed: Cuevas 1999 Proband M - Spain - - - - - 1 Jose Maria Millan
-/- 37 c.5156A>G r.(?) p.(Tyr1719Cys) - Parent #1 - benign g.76913457A>G g.77202412A>G - - MYO7A_000081 Heterozygous PubMed: Cuevas 1999; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs77625410 Germline - 0/68 controls +Tsp45I - - DNA SEQ - - USH1B ? PubMed: Cuevas 1999 Relative M - Spain - - - - - 1 Jose Maria Millan
-/- 37 c.5156A>G r.(?) p.(Tyr1719Cys) - Parent #2 - benign g.76913457A>G g.77202412A>G - - MYO7A_000081 Heterozygous PubMed: Jaijo 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs77625410 Germline - - +Tsp45I - - DNA SEQ - - USH1B ? PubMed: Jaijo 2006 Proband - - Spain - - - - - 1 Jose Maria Millan
-/- 37 c.5156A>G r.(?) p.(Tyr1719Cys) - Parent #2 - benign g.76913457A>G g.77202412A>G - - MYO7A_000081 Heterozygous PubMed: Janecke 1999, PubMed: Dad 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs77625410 Germline - 0/60 controls +Tsp45I - - DNA SEQ - - USH1B ? PubMed: Janecke 1999, PubMed: Dad 2016 Proband - - - - - - - - 1 Anne-Françoise Roux
-/- 37 c.5156A>G r.(?) p.(Tyr1719Cys) - Paternal (inferred) - benign g.76913457A>G g.77202412A>G - - MYO7A_000081 Heterozygous; unknown PubMed: Neveling 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs77625410 Germline - - +Tsp45I - - DNA SEQ, SEQ-NG-S - - RPar ? PubMed: Neveling 2012 Proband M - - - - - - - 1 Anne-Françoise Roux
-?/. - c.5156A>G r.(?) p.(Tyr1719Cys) - Parent #1 - likely benign g.76913457A>G g.77202412A>G - - MYO7A_000081 36 heterozygous, no homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs77625410 Germline - 36/2794 individuals - - - DNA arraySNP - Infinium Global Screening Array v1.0 ? - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - 36 Mohammed Faruq
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