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.

14 entries on 1 page. Showing entries 1 - 14.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

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DNA change (genomic) (hg19)     

DNA change (hg38)     

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DB-ID     

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+?/. 44 c.6028G>A r.(?) p.(Asp2010Asn) - Parent #2 - likely pathogenic g.76919825G>A g.77208780G>A - - MYO7A_000216 - PubMed: Zazo Seco 2017, Journal: Zazo Seco 2017 - - Germline - - - - - DNA SEQ-NG - - deafness - PubMed: Zazo Seco 2017, Journal: Zazo Seco 2017 - - - - - - - - - 1 Mieke Wesdorp
+?/? 44 c.6028G>A r.(?) p.(Asp2010Asn) FERM 2 (1902-2205) Parent #1 ACMG VUS g.76919825G>A g.77208780G>A - - MYO7A_000216 Heterozygous PubMed: Jacobson 2009; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ - - USH1B ? PubMed: Jacobson 2009 Proband M - - - - - - - 1 William J. Kimberling
+?/? 44 c.6028G>A r.(?) p.(Asp2010Asn) FERM 2 (1902-2205) Parent #1 ACMG VUS g.76919825G>A g.77208780G>A - - MYO7A_000216 Heterozygous; possible pathogenic PubMed: Yoshimura 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Yoshimura 2014 Proband - - Japan - - - - - 1 Anne-Françoise Roux
+?/+ 44 c.6028G>A r.(?) p.(Asp2010Asn) FERM2 (1902-2205) Maternal (confirmed) ACMG VUS g.76919825G>A g.77208780G>A - - MYO7A_000216 Homozygous; 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 - France - - - - - 1 Crystel Bonnet
+?/? 44 c.6028G>A r.(?) p.(Asp2010Asn) FERM2 (1902-2205) Paternal (confirmed) ACMG VUS g.76919825G>A g.77208780G>A - - MYO7A_000216 Homozygous; 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 - France - - - - - 1 Crystel Bonnet
+?/+ 44 c.6028G>A r.(?) p.(Asp2010Asn) FERM2 (1902-2205) Parent #1 ACMG VUS g.76919825G>A g.77208780G>A - - MYO7A_000216 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 - France - - - - - 1 Crystel Bonnet
+/. 44 c.6028G>A r.(?) p.(Asp2010Asn) - Unknown - pathogenic (recessive) g.76919825G>A - c.6028G>A - MYO7A_000216 2nd normal chromosome PubMed: Zong 2016 - - Germline yes - - - - DNA SEQ-NG, SEQ blood - Healthy/Control II-1 PubMed: Zong 2016 Healthy carrier (father) M no China chinese - - - - 1 LOVD
+/. 44 c.6028G>A r.(?) p.(Asp2010Asn) - Paternal (inferred) - pathogenic (recessive) g.76919825G>A - c.6028G>A - MYO7A_000216 - PubMed: Zong 2016 - - Germline yes - - - - DNA SEQ-NG, SEQ blood - retinal disease III-1 PubMed: Zong 2016 - M no China chinese - - - - 1 LOVD
+/. 44 c.6028G>A r.(?) p.(Asp2010Asn) - Paternal (inferred) - pathogenic (recessive) g.76919825G>A - c.6028G>A - MYO7A_000216 2nd normal chromosome PubMed: Zong 2016 - - Germline yes - - - - DNA SEQ-NG, SEQ blood - Healthy/Control III-2 PubMed: Zong 2016 Healthy carrier F no China chinese - - - - 1 LOVD
+/. 44 c.6028G>A r.(?) p.(Asp2010Asn) - Paternal (inferred) - pathogenic (recessive) g.76919825G>A - c.6028G>A - MYO7A_000216 - PubMed: Zong 2016 - - Germline yes - - - - DNA SEQ-NG, SEQ blood - retinal disease III-4 PubMed: Zong 2016 - M no China chinese - - - - 1 LOVD
+/. 44 c.6028G>A r.(?) p.(Asp2010Asn) - Paternal (inferred) - pathogenic (recessive) g.76919825G>A - c.6028G>A - MYO7A_000216 - PubMed: Zong 2016 - - Germline yes - - - - DNA SEQ-NG, SEQ blood - retinal disease III-5 PubMed: Zong 2016 - M no China chinese - - - - 1 LOVD
+?/. 44 c.6028G>A r.(?) p.(Asp2010Asn) - Maternal (confirmed) - likely pathogenic (recessive) g.76919825G>A - c.6028G>A - MYO7A_000216 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease CIC07289 PubMed: Khateb 2020 one affected daughter M yes - Father Moroccan and mother French - - - - 1 LOVD
+/. 44 c.6028G>A r.(?) p.(Asp2010Asn) - Both (homozygous) - pathogenic g.76919825G>A - c.6028G>A, p.(Asp2010Asn) - MYO7A_000216 - PubMed: Maia-2020 - - Germline yes - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Maia-2020 - M yes - - - - - - 1 LOVD
+?/. - c.6028G>A r.(?) p.(Asp2010Asn) - Unknown - likely pathogenic g.76919825G>A - - - MYO7A_000216 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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