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     

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Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

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ClinVar ID     

dbSNP ID     

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Disease     

ID_report     

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?/. - c.905G>A r.(?) p.(Arg302His) - Unknown - VUS g.76869378G>A g.77158332G>A MYO7A(NM_000260.3):c.905G>A (p.R302H), MYO7A(NM_000260.4):c.905G>A (p.R302H) - MYO7A_000003 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.905G>A r.(?) p.(Arg302His) - Unknown - likely benign g.76869378G>A g.77158332G>A MYO7A(NM_000260.3):c.905G>A (p.R302H), MYO7A(NM_000260.4):c.905G>A (p.R302H) - MYO7A_000003 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/? 9 c.905G>A r.(?) p.(Arg302His) Motor domain (1-729) Unknown ACMG likely benign g.76869378G>A g.77158332G>A - - MYO7A_000003 Heterozygous PubMed: Bujakowska 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs41298135 Germline - - -BsrBI;-AciI; - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Bujakowska 2014 Proband - - United States - - - - - 1 Anne-Françoise Roux
-?/? 9 c.905G>A r.(?) p.(Arg302His) Motor domain (1-729) Unknown ACMG likely benign g.76869378G>A g.77158332G>A - - MYO7A_000003 Heterozygous PubMed: Bujakowska 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs41298135 Germline - - -BsrBI;-AciI; - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Bujakowska 2014 Proband - - United States - - - - - 1 Anne-Françoise Roux
-?/? 9 c.905G>A r.(?) p.(Arg302His) Motor domain (1-729) Unknown ACMG likely benign g.76869378G>A g.77158332G>A - - MYO7A_000003 Heterozygous; UV1 PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs41298135 Germline - - -BsrBI;-AciI; - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-?/? 9 c.905G>A r.(?) p.(Arg302His) Motor domain (1-729) Paternal (inferred) ACMG likely benign g.76869378G>A g.77158332G>A - - MYO7A_000003 Homozygous PubMed: Weston 1996; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs41298135 Germline - 0/192 controls -BsrBI;-AciI; - - DNA SEQ - - USH1B ? PubMed: Weston 1996 Proband - - Belgium - - - - - 1 William J. Kimberling
+/+ 9 c.905G>A r.(?) p.(Arg302His) Motor domain (1-729) Maternal (inferred) ACMG likely benign g.76869378G>A g.77158332G>A - - MYO7A_000003 Homozygous PubMed: Weston 1996; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs41298135 Germline - 0/192 controls -BsrBI;-AciI; - - DNA SEQ - - USH1B ? PubMed: Weston 1996 Proband - - Belgium - - - - - 1 William J. Kimberling
-?/? 9 c.905G>A r.(?) p.(Arg302His) Motor domain (1-729) Unknown ACMG likely benign g.76869378G>A g.77158332G>A - - MYO7A_000003 Heterozygous PubMed: Weston 1996; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs41298135 Germline - 0/192 controls -BsrBI;-AciI; - - DNA SEQ - - USH1B ? PubMed: Weston 1996 Proband - - Netherlands - - - - - 1 William J. Kimberling
-?/? 9 c.905G>A r.(?) p.(Arg302His) Motor domain (1-729) Parent #1 ACMG likely benign g.76869378G>A g.77158332G>A - - MYO7A_000003 Heterozygous PubMed: Weston 1996; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs41298135 Germline - 0/192 controls -BsrBI;-AciI; - - DNA SEQ - - USH1B ? PubMed: Weston 1996 Proband - - Netherlands - - - - - 1 William J. Kimberling
-?/? 9 c.905G>A r.(?) p.(Arg302His) Motor domain (1-729) Parent #2 ACMG likely benign g.76869378G>A g.77158332G>A - - MYO7A_000003 Heterozygous PubMed: Pennings 2004; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs41298135 Germline - - -BsrBI;-AciI; - - DNA SEQ - - USH1B ? PubMed: Pennings 2004 Proband - - Netherlands - - - - - 1 Anne-Françoise Roux
-?/? 9 c.905G>A r.(?) p.(Arg302His) Motor domain (1-729) Unknown ACMG likely benign g.76869378G>A g.77158332G>A - - MYO7A_000003 Heterozygous PubMed: Weston 1996; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs41298135 Germline - 0/192 controls -BsrBI;-AciI; - - DNA SEQ - - USH1B ? PubMed: Weston 1996 Proband - - Sweden - - - - - 1 William J. Kimberling
-?/? 9 c.905G>A r.(?) p.(Arg302His) Motor domain (1-729) Unknown ACMG likely benign g.76869378G>A g.77158332G>A - - MYO7A_000003 Heterozygous; non pathogenic PubMed: Vozzi 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs41298135 Germline - - -BsrBI;-AciI; - - DNA PE, SEQ - APEX USH2 ? PubMed: Vozzi 2011 Proband - - Italy - - - - - 1 Anne-Françoise Roux
?/. - c.905G>A r.(?) p.(Arg302His) - Unknown - VUS g.76869378G>A g.77158332G>A MYO7A(NM_000260.3):c.905G>A (p.R302H), MYO7A(NM_000260.4):c.905G>A (p.R302H) - MYO7A_000003 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. 9 c.905G>A r.(?) p.(Arg302His) - Parent #1 - pathogenic g.76869378G>A g.77158332G>A - - MYO7A_000003 unknown variant 2nd chromosome PubMed: Cremers 2007 - - Germline - - - - - DNA PE - - retinal disease USH1-25 PubMed: Cremers 2007 - F no Denmark - - - - - 1 LOVD
+?/. - c.905G>A r.(?) p.(Arg302His) - Unknown - likely pathogenic g.76869378G>A g.77158332G>A - - MYO7A_000003 - PubMed: Ellingford 2016 - - Germline - - - - - DNA SEQ - 105-gene panel retinal disease 12000202 PubMed: Ellingford 2016 familial segregation analysis requested - - - - - - - - 1 LOVD
?/. - c.905G>A r.(?) p.(Arg302His) - Unknown - VUS g.76869378G>A - - - MYO7A_000003 - PubMed: Velde 2022, Journal: Velde 2022 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease PatD;071951 PubMed: Velde 2022, Journal: Velde 2022, PubMed: de Bruijn 2023 - M - Ireland white - - - - 1 Janine Reurink
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