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.

10 entries on 1 page. Showing entries 1 - 10.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

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DNA change (hg38)     

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Reference     

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Disease     

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+/. 17 c.1969C>T r.(?) p.(Arg657Trp) - Paternal (confirmed) - pathogenic g.76885835C>T g.77174789C>T - - MYO7A_000410 2/133 hearing Turkish Jews, 0/177 Jewish controls of other origins PubMed: Brownstein 2014, Journal: Brownstein 2014 - - Germline yes 2/170 cases - - - DNA SEQ-NG-I blood - DFNB2 - PubMed: Brownstein 2014, Journal: Brownstein 2014 2-generation family, 1 affected, unaffected heterozygous carrier parents M no Israel Turkey;Jewish - - - - 1 Zippi Brownstein
+/. 17 c.1969C>T r.(?) p.(Arg657Trp) - Unknown - pathogenic g.76885835C>T g.77174789C>T - - MYO7A_000410 2/310 controls (heterozygous) PubMed: Brownstein 2014, Journal: Brownstein 2014 - - Germline yes 2/170 cases - - - DNA SEQ-NG-I blood - DFNB2 - PubMed: Brownstein 2014, Journal: Brownstein 2014 - - no Israel Jewish-Ashkenazi - - - - 1 Zippi Brownstein
+/. 17 c.1969C>T r.(?) p.(Arg657Trp) - Unknown - pathogenic g.76885835C>T g.77174789C>T - - MYO7A_000410 - PubMed: Brownstein 2014, Journal: Brownstein 2014 - - Germline - 2/310 controls (het) - - - DNA SEQ - - Healthy/Control - PubMed: Brownstein 2014, Journal: Brownstein 2014 310 controls - - Israel - - - - - 2 Johan den Dunnen
+?/? 17 c.1969C>T r.(?) p.(Arg657Trp) Motor domain (1-729) Maternal (confirmed) ACMG VUS g.76885835C>T g.77174789C>T - - MYO7A_000410 Heterozygous; UV1 PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/878 controls -BbvI;-Fnu4HI;-MwoI;-ApeKI;-TseI;-AciI; - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+?/? 17 c.1969C>T r.(?) p.(Arg657Trp) Motor domain (1-729) Maternal (confirmed) ACMG VUS g.76885835C>T g.77174789C>T - - MYO7A_000410 Heterozygous; mutation PubMed: Zhai 2015; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/200 controls -BbvI;-Fnu4HI;-MwoI;-ApeKI;-TseI;-AciI; - - DNA SEQ, SEQ-NG-S - - USH2 ? PubMed: Zhai 2015 Proband M - China - - - - - 1 Anne-Françoise Roux
+?/? 17 c.1969C>T r.(?) p.(Arg657Trp) Motor domain (1-729) Parent #1 ACMG VUS g.76885835C>T g.77174789C>T - - MYO7A_000410 Heterozygous; mutation PubMed: Jiang 2015; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - -BbvI;-Fnu4HI;-MwoI;-ApeKI;-TseI;-AciI; - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Jiang 2015 Proband M - China - - - - - 1 Anne-Françoise Roux
+?/+ 17 c.1969C>T r.(?) p.(Arg657Trp) Motor domain (1-729) Parent #2 ACMG VUS g.76885835C>T g.77174789C>T - - MYO7A_000410 Heterozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband M - Italy - - - - - 1 Crystel Bonnet
+?/. - c.1969C>T r.(?) p.(Arg657Trp) - Unknown - likely pathogenic g.76885835C>T - - - MYO7A_000410 - - - rs878853236 CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. 17 c.1969C>T r.(?) p.(Arg657Trp) - Unknown ACMG pathogenic (recessive) g.76885835C>T - - - MYO7A_000410 - PubMed: Bahena 2021 - - Germline yes - - - - DNA SEQ-NG-I - Exome sequencing USH1B Pat1 PubMed: Bahena 2021 - F yes Iran - - - - - 1 Barbara Vona
+/. 17 c.1969C>T r.(?) p.(Arg657Trp) - Both (homozygous) - pathogenic g.76885835C>T - c.1969C>T - MYO7A_000410 - PubMed: Colombo-2020 - rs878853236 Germline - - - - - DNA SEQ - - retinal disease - PubMed: Colombo-2020 - M no - - - - - - 1 LOVD
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