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.

6 entries on 1 page. Showing entries 1 - 6.
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     
-?/. - c.12505A>G r.(?) p.(Thr4169Ala) - Unknown - likely benign g.215848748T>C g.215675406T>C USH2A(NM_206933.2):c.12505A>G (p.T4169A), USH2A(NM_206933.4):c.12505A>G (p.T4169A) - USH2A_000604 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/? 63 c.12505A>G r.(?) p.(Thr4169Ala) Fibronectin type-III 27 (4154-4258) Unknown ACMG likely benign g.215848748T>C g.215675406T>C - - USH2A_000604 Heterozygous; UV1 PubMed: Le Quesne Stabej 2012, USMA missense analysis, missense variant in MSV3d - rs113107803 Germline - 0/878 controls +EciI;+AciI;-Hpy166II;-CspCI; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
?/. - c.12505A>G r.(?) p.(Thr4169Ala) - Unknown - VUS g.215848748T>C g.215675406T>C USH2A(NM_206933.2):c.12505A>G (p.T4169A), USH2A(NM_206933.4):c.12505A>G (p.T4169A) - USH2A_000604 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.12505A>G r.(?) p.(Thr4169Ala) - Unknown - likely benign g.215848748T>C g.215675406T>C USH2A(NM_206933.2):c.12505A>G (p.T4169A), USH2A(NM_206933.4):c.12505A>G (p.T4169A) - USH2A_000604 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.12505A>G r.(?) p.(Thr4169Ala) - Both (homozygous) - pathogenic (recessive) g.215848748T>C - 1:215848748T>C ENST00000307340.3:c.12505A>G (Thr4169Ala) - USH2A_000604 - PubMed: Carss 2017 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease G007706 PubMed: Carss 2017 - F - United Kingdom (Great Britain) Europe - - - - 1 LOVD
+?/. - c.12505A>G r.(?) p.(Thr4169Ala) - Both (homozygous) - likely pathogenic g.215848748T>C g.215675406T>C USH2A c.12505A>G, p.Thr4169Ala - USH2A_000604 homozygous PubMed: Turro 2020 - - Germline/De novo (untested) ? - - - - DNA SEQ-NG-I blood whole genome sequencing retinal disease G007706 PubMed: Turro 2020 only individuals with mutations in retinal disease genes from this publication were inserted into LOVD ? - (United Kingdom (Great Britain)) - - - - - 1 LOVD
Legend   How to query  

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


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.