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.

20 entries on 1 page. Showing entries 1 - 20.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

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Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

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Re-site     

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Methylation     

Template     

Technique     

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Disease     

ID_report     

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Owner     
+?/. - c.3763del r.(?) p.(Lys1255Argfs*8) - Unknown - likely pathogenic g.76901755del g.77190710del , c.3763del, p.Lys1255ArgfsTer8 - MYO7A_000165 - PubMed: Ezquerra-Inchausti 2018 - - Germline yes - - - - DNA SEQ-NG blood - retinal disease II:3 PubMed: Ezquerra-Inchausti 2018 Family RP88, II:3 ? no Spain - - - - - 1 LOVD
+?/. - c.3763del r.(?) p.(Lys1255Argfs*8) - Unknown - likely pathogenic g.76901755del g.77190710del , c.3763del, p.Lys1255ArgfsTer8 - MYO7A_000165 - PubMed: Ezquerra-Inchausti 2018 - - Germline yes - - - - DNA SEQ-NG blood - retinal disease II:5 PubMed: Ezquerra-Inchausti 2018 Family RP88, II:5 ? no Spain - - - - - 1 LOVD
+/+ 30 c.3764del r.(?) p.(Lys1255Argfs*8) - Unknown - pathogenic g.76901755del g.77190710del - - MYO7A_000165 Heterozygous PubMed: Le Quesne Stabej 2012 - rs111033347 Germline - - +Hpy188III - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/+ 30 c.3764del r.(?) p.(Lys1255Argfs*8) - Unknown - pathogenic g.76901755del g.77190710del - - MYO7A_000165 Heterozygous PubMed: Le Quesne Stabej 2012 - rs111033347 Germline - - +Hpy188III - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/+ 30 c.3764del r.(?) p.(Lys1255Argfs*8) - Maternal (confirmed) - pathogenic g.76901755del g.77190710del - - MYO7A_000165 Heterozygous PubMed: Le Quesne Stabej 2012 - rs111033347 Germline - - +Hpy188III - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/+ 30 c.3764del r.(?) p.(Lys1255Argfs*8) - Parent #1 - pathogenic g.76901755del g.77190710del 3764delA - MYO7A_000165 Heterozygous PubMed: Jaijo 2007 - rs111033347 Germline - - +Hpy188III - - DNA SEQ - - USH1B ? PubMed: Jaijo 2007 Proband F - Spain - - - - - 1 Jose Maria Millan
+/+ 30 c.3764del r.(?) p.(Lys1255Argfs*8) - Parent #1 - pathogenic g.76901755del g.77190710del 3764delA - MYO7A_000165 Heterozygous PubMed: Roux 2011 - rs111033347 Germline - - +Hpy188III - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband M - Portugal - - - - - 1 Anne-Françoise Roux
+/+ 30 c.3764del r.(?) p.(Lys1255Argfs*8) - Unknown - pathogenic g.76901755del g.77190710del 3764delA - MYO7A_000165 Heterozygous PubMed: Besnard, Garcia-Garcia 2014 - rs111033347 Germline - - +Hpy188III - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Besnard, Garcia-Garcia 2014 Proband - - Spain - - - - - 1 Anne-Françoise Roux
+/+ 30 c.3764del r.(?) p.(Lys1255Argfs*8) - Parent #2 - pathogenic g.76901755del g.77190710del 3764delA - MYO7A_000165 Heterozygous; mutation PubMed: Bonnet 2016 - rs111033347 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband M - Germany - - - - - 1 Crystel Bonnet
+/+ 30 c.3764del r.(?) p.(Lys1255Argfs*8) - Parent #2 - pathogenic g.76901755del g.77190710del 3764delA - MYO7A_000165 Heterozygous; mutation PubMed: Bonnet 2016 - rs111033347 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+/. - c.3764del r.(?) p.(Lys1255Argfs*8) - Both (homozygous) - pathogenic g.76901755del g.77190710del 3764delA - MYO7A_000165 - PubMed: Neuhaus 2017 - - Germline yes - - - - DNA SEQ-NG - gene panel USH Pat99 PubMed: Neuhaus 2017 - - no Germany - - - - - 1 LOVD
+/. - c.3764del r.(?) p.(Lys1255Argfs*8) - Unknown - pathogenic g.76901755del g.77190710del MYO7A c.3764delA, p.Lys1255ArgfsTer8 - MYO7A_000165 heterozygous PubMed: Turro 2020 - - Germline/De novo (untested) ? - - - - DNA SEQ-NG-I blood whole genome sequencing retinal disease G004992 PubMed: Turro 2020 only individuals with mutations in retinal disease genes from this publication were inserted into LOVD ? - (United Kingdom (Great Britain)) - - - - - 1 LOVD
+?/. 30 c.3764del r.(?) p.(Lys1255Argfs*8) - Parent #2 - likely pathogenic (recessive) g.76901755del - c.3764del p.Lys1255Argfs*8 - MYO7A_000165 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease CIC05503 PubMed: Khateb 2020 simplex case M - - French - - - - 1 LOVD
+/. 30 c.3764del r.(?) p.(Lys1255Argfs*8) - Parent #2 - pathogenic g.76901755del - c.3764delA - MYO7A_000165 - PubMed: Galbis-Martinez-2021 - - Germline - - - - - DNA ? - - retinal disease - PubMed: Galbis-Martinez-2021 - - - - - - - - - 4 LOVD
+/. 30 c.3764del r.(?) p.(Lys1255Argfs*8) - Parent #1 - pathogenic g.76901755del - c.3764delA - MYO7A_000165 - PubMed: Galbis-Martinez-2021 - - Germline - - - - - DNA ? - - retinal disease - PubMed: Galbis-Martinez-2021 - - - - - - - - - 4 LOVD
+/. 30 c.3764del r.(?) p.(Lys1255Argfs*8) - Both (homozygous) - pathogenic g.76901755del - c.3764delA - MYO7A_000165 - PubMed: Galbis-Martinez-2021 - - Germline - - - - - DNA ? - - retinal disease - PubMed: Galbis-Martinez-2021 - - - - - - - - - 4 LOVD
+/. - c.3764delA r.(?) p.(Lys1255ArgfsTer8) - Unknown ACMG pathogenic g.76901755del - - - MYO7A_000165 - PubMed: Mansard et al, 2021 - rs111033347 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - M - - - - - - - 1 Anne-Françoise Roux
+/. - c.3764delA r.(?) p.(Lys1255ArgfsTer8) - Unknown ACMG pathogenic g.76901755del - - - MYO7A_000165 - PubMed: Mansard et al, 2021 - rs111033347 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
+/. - c.3764delA r.(?) p.(Lys1255ArgfsTer8) - Maternal (confirmed) ACMG pathogenic g.76901755del - - - MYO7A_000165 - PubMed: Mansard et al, 2021 - rs111033347 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - M - - - - - - - 1 Anne-Françoise Roux
+/. - c.3764delA r.(?) p.(Lys1255ArgfsTer8) - Paternal (confirmed) ACMG pathogenic g.76901755del - - - MYO7A_000165 - PubMed: Mansard et al, 2021 - rs111033347 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - M - - - - - - - 1 Anne-Françoise Roux
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