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.

11 entries on 1 page. Showing entries 1 - 11.
Legend   How to query  

Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
-?/? 62i c.12295-3T>A r.spl? p.? - Unknown ACMG VUS g.215848961A>T g.215675619A>T - - USH2A_000625 Heterozygous; UV2 PubMed: Le Quesne Stabej 2012 - rs111033518 Germline - 0/96 controls +BbsI;+Hpy188I;+AcuI;-Hpy166II;-AccI;-SfcI; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+?/? 62i c.12295-3T>A r.spl? p.? - Unknown ACMG VUS g.215848961A>T g.215675619A>T - - USH2A_000625 Heterozygous PubMed: Lenassi 2015 - rs111033518 Germline - - +BbsI;+Hpy188I;+AcuI;-Hpy166II;-AccI;-SfcI; - - DNA SEQ - - RPar - PubMed: Lenassi 2015 Proband - - United Kingdom (Great Britain) - - - - - 1 Eva Lenassi
+?/? 62i c.12295-3T>A r.spl? p.? - Unknown ACMG VUS g.215848961A>T g.215675619A>T - - USH2A_000625 Heterozygous PubMed: Lenassi 2015 - rs111033518 Germline - - +BbsI;+Hpy188I;+AcuI;-Hpy166II;-AccI;-SfcI; - - DNA SEQ - - RPar - PubMed: Lenassi 2015 Relative - - United Kingdom (Great Britain) - - - - - 1 Eva Lenassi
+?/? 62i c.12295-3T>A r.spl? p.? - Unknown ACMG VUS g.215848961A>T g.215675619A>T - - USH2A_000625 Heterozygous PubMed: Lenassi 2015 - rs111033518 Germline - - +BbsI;+Hpy188I;+AcuI;-Hpy166II;-AccI;-SfcI; - - DNA SEQ - - RPar - PubMed: Lenassi 2015 Proband - - United Kingdom (Great Britain) - - - - - 1 Eva Lenassi
+?/? 62i c.12295-3T>A r.spl? p.? - Unknown ACMG VUS g.215848961A>T g.215675619A>T - - USH2A_000625 Heterozygous PubMed: Lenassi 2015 - rs111033518 Germline - - +BbsI;+Hpy188I;+AcuI;-Hpy166II;-AccI;-SfcI; - - DNA SEQ - - RPar - PubMed: Lenassi 2015 Proband - - United Kingdom (Great Britain) - - - - - 1 Eva Lenassi
+?/. - c.12295-3T>A r.spl p.? - Parent #1 - likely pathogenic g.215848961A>T g.215675619A>T IVS62-3T>A - USH2A_000625 - PubMed: Stone 2017 - - Germline - - - - - DNA SEQ-NG - - retinal disease 586 PubMed: Stone 2017 1 affected F - (United States) - - - - - 1 LOVD
+?/. - c.12295-3T>A r.spl? p.(?) - Unknown - likely pathogenic g.215848961A>T g.215675619A>T USH2A c.12295-3T>A - USH2A_000625 heterozygous PubMed: Zampaglione 2020 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ blood - retinal disease 001-465 PubMed: Zampaglione 2020 - ? - - - - - - - 1 LOVD
+?/. - c.12295-3T>A r.spl? p.(?) - Parent #1 - likely pathogenic g.215848961A>T g.215675619A>T USH2A, variant 1: c.12295-3T>A/p.?, variant 2: c.55del/p.M19Cfs*2 - USH2A_000625 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET7 targeted sequencing panel - see paper retinal disease 1174 PubMed: Weisschuh 2020 Filing key number: 851, sporadic retinitis pigmentosa, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
+/. 62i c.12295-3T>A r.spl? p.(?) - Parent #2 - pathogenic g.215848961A>T - c.12295-3T>A - USH2A_000625 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - F - - - - - - - 1 Daan Panneman
+/. 62i c.12295-3T>A r.12295_13811del p.(Thr4099ValfsTer2) - Parent #1 ACMG pathogenic g.215848961A>T g.215675619A>T - - USH2A_000625 no variant 2nd chromome PubMed: Reurink 2023, Journal: Reurink 2023 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease arRP23 PubMed: Reurink 2023, Journal: Reurink 2023 - - - - - - - - - 1 Janine Reurink
+/. - c.12295-3T>A r.spl p.? - Unknown ACMG pathogenic g.215848961A>T g.215675619A>T - - USH2A_000625 ACMG GN005 criteria: PM2_P PM3_S PP1_P PP3_P PubMed: Lenassi, E. et al., 2015; PubMed: Le Quesne Stabej, P. et al., 2012; PubMed: Weisschuh, N. et al., 2020 - rs111033518 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
Legend   How to query  

All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.