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.

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

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Disease     

ID_report     

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Owner     
+/. - c.11875_11876del r.(?) p.(Gln3959AsnfsTer53) - Unknown - pathogenic g.215901565_215901566del g.215728223_215728224del USH2A(NM_206933.4):c.11875_11876delCA (p.Q3959Nfs*53) - USH2A_000276 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/+ 61 c.11875_11876del r.(?) p.(Gln3959Asnfs*53) Fibronectin type-III 24 (3863-3960) Unknown - pathogenic g.215901565_215901566del g.215728223_215728224del 11875_11876delCA - USH2A_000276 Heterozygous; Pathogenic PubMed: Le Quesne Stabej 2012 - - Germline - 0/878 controls none - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/+ 61 c.11875_11876del r.(?) p.(Gln3959Asnfs*53) Fibronectin type-III 24 (3863-3960) Unknown - pathogenic g.215901565_215901566del g.215728223_215728224del 11875_11876delCA - USH2A_000276 Heterozygous; Pathogenic PubMed: Le Quesne Stabej 2012 - - Germline - 0/878 controls none - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/+ 61 c.11875_11876del r.(?) p.(Gln3959Asnfs*53) Fibronectin type-III 24 (3863-3960) Paternal (confirmed) - pathogenic g.215901565_215901566del g.215728223_215728224del 11875_11876delCA - USH2A_000276 Heterozygous PubMed: Baux 2014 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband F - Italy - - - - - 1 Anne-Françoise Roux
+/+ 61 c.11875_11876del r.(?) p.(Gln3959Asnfs*53) Fibronectin type-III 24 (3863-3960) Unknown - pathogenic g.215901565_215901566del g.215728223_215728224del 11875_11876delCA - USH2A_000276 Heterozygous PubMed: Baux 2014 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband M - France - - - - - 1 Anne-Françoise Roux
+/+ 61 c.11875_11876del r.(?) p.(Gln3959Asnfs*53) Fibronectin type-III 24 (3863-3960) Maternal (confirmed) - pathogenic g.215901565_215901566del g.215728223_215728224del 11875_11876delCA - USH2A_000276 Heterozygous PubMed: Baux 2014 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband M - France - - - - - 1 Anne-Françoise Roux
+/+ 61 c.11875_11876del r.(?) p.(Gln3959Asnfs*53) Fibronectin type-III 24 (3863-3960) Paternal (confirmed) - pathogenic g.215901565_215901566del g.215728223_215728224del 11875_11876delCA - USH2A_000276 Heterozygous PubMed: Baux 2014 - - Germline - - - - - DNA SEQ - - USH3 - PubMed: Baux 2014 Proband M - France - - - - - 1 Anne-Françoise Roux
+/+ 61 c.11875_11876del r.(?) p.(Gln3959Asnfs*53) Fibronectin type-III 24 (3863-3960) Parent #2 - pathogenic g.215901565_215901566del g.215728223_215728224del 11875_11876delCA - USH2A_000276 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband M - France - - - - - 1 Crystel Bonnet
+/. - c.11875_11876del r.(?) p.(Gln3959AsnfsTer53) - Unknown - pathogenic g.215901565_215901566del g.215728223_215728224del USH2A(NM_206933.4):c.11875_11876delCA (p.Q3959Nfs*53) - USH2A_000276 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.11875_11876del r.(?) p.(Gln3959Asnfs*53) - Unknown - pathogenic (recessive) g.215901562_215901563del - 1:215901561TTG>T ENST00000307340.3:c.11875_11876delCA (Gln3959AsnfsTer53) - USH2A_000276 - PubMed: Carss 2017 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease W000333 PubMed: Carss 2017 - M - United Kingdom (Great Britain) Europe - - - - 1 LOVD
+?/. - c.11875_11876del r.(?) p.(Gln3959Asnfs*53) - Parent #1 - likely pathogenic g.215901565_215901566del g.215728223_215728224del 11872_11873delAC - USH2A_000276 - PubMed: Stone 2017 - - Germline - - - - - DNA SEQ-NG - - retinal disease 589 PubMed: Stone 2017 1 affected M - (United States) - - - - - 1 LOVD
+?/. - c.11875_11876del r.(?) p.(Gln3959Asnfs*53) - Unknown - likely pathogenic g.215901565_215901566del g.215728223_215728224del 11875_11876delCA - USH2A_000276 - PubMed: Ellingford 2016 - - Germline - - - - - DNA SEQ - 105-gene panel retinal disease 13008826 PubMed: Ellingford 2016 patient - - - - - - - - 1 LOVD
+/. - c.11875_11876del r.(?) p.(Gln3959Asnfs*53) - Unknown - pathogenic g.215901565_215901566del g.215728223_215728224del USH2A c.11875_11876del, p.Gln3959AsnfsTer53 - USH2A_000276 heterozygous PubMed: Zampaglione 2020 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ blood - retinal disease 121-193 PubMed: Zampaglione 2020 - ? - - - - - - - 1 LOVD
+/. - c.11875_11876del r.(?) p.(Gln3959Asnfs*53) - Unknown - pathogenic g.215901565_215901566del g.215728223_215728224del c.11875_11876del, p.Gln3959AsnfsTer53 - USH2A_000276 heterozygous PubMed: Zampaglione 2020 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ blood - retinal disease 121-178 PubMed: Zampaglione 2020 - ? - - - - - - - 1 LOVD
+/. - c.11875_11876del r.(?) p.(Gln3959Asnfs*53) - Unknown - pathogenic g.215901565_215901566del g.215728223_215728224del USH2A c.11875_11876delCA, p.Gln3959AsnfsTer53 - USH2A_000276 heterozygous PubMed: Turro 2020 - - Germline/De novo (untested) ? - - - - DNA SEQ-NG-I blood whole genome sequencing retinal disease W000333 PubMed: Turro 2020 only individuals with mutations in retinal disease genes from this publication were inserted into LOVD ? - - - - - - - 1 LOVD
+?/. - c.11875_11876del r.(?) p.(Gln3959Asnfs*53) - Parent #2 - likely pathogenic g.215901565_215901566del g.215728223_215728224del USH2A c.11875_11876del - USH2A_000276 protein variant annotation not written; heterozygous PubMed: Toms 2020 - - Unknown ? - - - - ? ? - retrospective cohort retinal disease 28 PubMed: Toms 2020 - ? - United Kingdom (Great Britain) - - - - - 1 LOVD
+/. 61 c.11875_11876del r.(?) p.(Gln3959Asnfs*53) - Parent #2 - pathogenic g.215901562_215901563del - c.11875_11876del - USH2A_000276 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - F - - - - - - - 1 Daan Panneman
+/. - c.11875_11876del r.(?) p.(Gln3959AsnfsTer53) - Unknown ACMG pathogenic g.215901565_215901566del g.215728223_215728224del 11875_11876delCA - USH2A_000276 ACMG GN005 criteria: PVS1_VS PM2_P PM3_S PubMed: Bonnet, C. et al., 2016; PubMed: Le Quesne Stabej, P. et al., 2012; PubMed: Wafa, T. T. et al., 2021; PubMed: Mansard, L. et al., 2021 - rs779791079 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.11875_11876delCA r.(?) p.(Gln3959AsnfsTer53) - Unknown ACMG pathogenic g.215901562_215901563del - - - USH2A_000276 - PubMed: Mansard et al, 2021 - rs779791079 Germline - - - - - DNA SEQ-NG, SEQ - - USH2A - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
+?/. 61 c.11875_11876delCA r.(?) p.(Gln3959Asnfs*53) - Unknown - likely pathogenic g.215901562_215901563delTG - c.11875_1876delCA, p.Q3959Nfs*53 - USH2A_000276 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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