Full data view for gene USH2A


This database is one of the ”Retinal and hearing impairment genetic variant databases”.
Information The variants shown are described using the NM_206933.2 transcript reference sequence.

18 entries on 1 page. Showing entries 1 - 18.
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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)     

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ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

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Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

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Consanguinity     

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VIP     

Data_av     

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Panel size     

Owner     
+/+ 55 c.10759C>T r.(?) p.(Gln3587*) - Paternal (inferred) - pathogenic g.215953365G>A g.215780023G>A - - USH2A_000128 Homozygous PubMed: Baux 2007 - rs111033418 Germline - - +DdeI;+Bsu36I;-BsaJI;-StyI; - - DNA SEQ - - USH2 - PubMed: Baux 2007 Proband M - France - - - - - 1 Anne-Françoise Roux
+/+ 55 c.10759C>T r.(?) p.(Gln3587*) - Maternal (inferred) - pathogenic g.215953365G>A g.215780023G>A - - USH2A_000128 Homozygous PubMed: Baux 2007 - rs111033418 Germline - - +DdeI;+Bsu36I;-BsaJI;-StyI; - - DNA SEQ - - USH2 - PubMed: Baux 2007 Proband M - France - - - - - 1 Anne-Françoise Roux
+/+ 55 c.10759C>T r.(?) p.(Gln3587*) - Parent #2 - pathogenic g.215953365G>A g.215780023G>A - - USH2A_000128 Heterozygous; Pathogenic PubMed: Jaijo 2010 - rs111033418 Germline - - +DdeI;+Bsu36I;-BsaJI;-StyI; - - DNA SEQ, SSCA - - USH2 - PubMed: Jaijo 2010 Proband F - Spain - - - - - 1 Jose Maria Millan
+/+ 55 c.10759C>T r.(?) p.(Gln3587*) - Parent #2 - pathogenic g.215953365G>A g.215780023G>A - - USH2A_000128 Heterozygous PubMed: Le Guédard-Méreuze 2010 - rs111033418 Germline - - +DdeI;+Bsu36I;-BsaJI;-StyI; - - DNA minigene, SEQ - - USH2 - PubMed: Le Guédard-Méreuze 2010 Proband F - France - - - - - 1 Anne-Françoise Roux
+/+ 55 c.10759C>T r.(?) p.(Gln3587*) - Maternal (confirmed) - pathogenic g.215953365G>A g.215780023G>A - - USH2A_000128 Heterozygous PubMed: Baux 2014 - rs111033418 Germline - - +DdeI;+Bsu36I;-BsaJI;-StyI; - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband F - France - - - - - 1 Anne-Françoise Roux
+/+ 55 c.10759C>T r.(?) p.(Gln3587*) - Maternal (confirmed) - pathogenic g.215953365G>A g.215780023G>A - - USH2A_000128 Heterozygous PubMed: Baux 2014 - rs111033418 Germline - - +DdeI;+Bsu36I;-BsaJI;-StyI; - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband F - France - - - - - 1 Anne-Françoise Roux
+/+ 55 c.10759C>T r.(?) p.(Gln3587*) - Parent #2 - pathogenic g.215953365G>A g.215780023G>A - - USH2A_000128 Heterozygous; Neutral PubMed: Garcia-Garcia 2011 - rs111033418 Germline - - +DdeI;+Bsu36I;-BsaJI;-StyI; - - DNA SEQ, SSCA - - USH2 - PubMed: Garcia-Garcia 2011 Proband M - Spain - - - - - 1 Jose Maria Millan
+/+ 55 c.10759C>T r.(?) p.(Gln3587*) - Parent #1 - pathogenic g.215953365G>A g.215780023G>A - - USH2A_000128 Heterozygous; mutation PubMed: Bonnet 2016 - rs111033418 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband F - France - - - - - 1 Crystel Bonnet
+/. - c.10759C>T r.(?) p.(Gln3587*) - Parent #1 - pathogenic g.215953365G>A g.215780023G>A - - USH2A_000128 - PubMed: Neuhaus 2017 - rs111033418 Germline - - - - - DNA SEQ-NG - gene panel USH Pat66 PubMed: Neuhaus 2017 - - no Germany - - - - - 1 LOVD
+?/. - c.10759C>T r.(?) p.(Gln3587*) - Unknown - likely pathogenic g.215953365G>A g.215780023G>A - - USH2A_000128 - PubMed: Perez-Carro 2018 - - Germline ? - - - - DNA SEQ-NG blood - retinal disease RP-2424 PubMed: Perez-Carro 2018 family RP-2424 ? ? Spain - - - - - 1 LOVD
+?/. 55 c.10759C>T r.(?) p.(Gln3587*) - Unknown - likely pathogenic g.215953365G>A g.215780023G>A USH2A Ex.13 c.2276G>T p.(Cys759Phe), Ex.55 c.10759C>T p.(Gln3587*) - USH2A_000128 compound heterozygous PubMed: Martin Merida 2019 - - Germline yes - - - - DNA SEQ-NG-I - - retinal disease RP-2424 PubMed: Martin Merida 2019 - ? - Spain - - - - - 1 LOVD
+?/. - c.10759C>T r.(?) p.(Gln3587*) - Parent #2 - likely pathogenic g.215953365G>A g.215780023G>A USH2A c.10759C>T, p.Q3587X - USH2A_000128 compound heterozygous PubMed: Jauregui 2020 - - Unknown ? - - - - DNA SEQ-NG blood targeted sequencing retinal disease 119 PubMed: Jauregui 2020 - F - (United States) white - - - - 1 LOVD
+/. - c.10759C>T r.(?) p.(Gln3587Ter) - Paternal (confirmed) ACMG pathogenic g.215953365G>A - - - USH2A_000128 - PubMed: Mansard et al, 2021 - rs111033418 Germline - - - - - DNA SEQ-NG, SEQ - - USH2A - PubMed: Mansard et al, 2021 - M - - - - - - - 1 Anne-Françoise Roux
+/. - c.10759C>T r.(?) p.(Gln3587Ter) - Unknown ACMG pathogenic g.215953365G>A - - - USH2A_000128 - PubMed: Mansard et al, 2021 - rs111033418 Germline - - - - - DNA SEQ-NG, SEQ - - USH2A - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
+/. 55 c.10759C>T r.(?) p.(Gln3587*) - Parent #2 - pathogenic g.215953365G>A - c.10759C>T - USH2A_000128 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - M - - - - - - - 1 Daan Panneman
+/. - c.10759C>T r.(?) p.(Gln3587Ter) - Unknown ACMG pathogenic g.215953365G>A g.215780023G>A - - USH2A_000128 ACMG GN005 criteria: PVS1_VS PM2_P PM3_P PubMed: Bonnet, C. et al., 2016; PubMed: Garcia-Garcia, G. et al., 2011; PubMed: Mansard, L. et al., 2021; PubMed: Jauregui, R. et al., 2020; PubMed: Neuhaus, C. et al., 2017 - rs111033418 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.10759C>T r.(?) p.(Gln3587Ter) - Unknown ACMG pathogenic (recessive) g.215953365G>A g.215780023G>A - - USH2A_000128 ACMG PM2, PVS1, PP5 PubMed: Weisschuh 2024 - - Germline - - - - - DNA SEQ-NG - WGS ? USHII-307 PubMed: Weisschuh 2024 patient, no family history F - Germany - - - - - 1 Johan den Dunnen
+/. - c.10759C>T r.(?) p.(Gln3587Ter) - Unknown ACMG pathogenic (recessive) g.215953365G>A g.215780023G>A - - USH2A_000128 ACMG PM2, PVS1, PP5 PubMed: Weisschuh 2024 48357 - Germline - - - - - DNA SEQ-NG - WGS ? USHII-324 PubMed: Weisschuh 2024 patient M - Germany - - - - - 1 Johan den Dunnen
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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