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.

5 entries on 1 page. Showing entries 1 - 5.
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     
+?/? 53 c.10585G>A r.(?) p.(Gly3529Ser) Fibronectin type-III 20 (3499-3585) Unknown ACMG VUS g.215956080C>T g.215782738C>T - - USH2A_000431 Heterozygous; UV3 PubMed: Le Quesne Stabej 2012, USMA missense analysis, missense variant in MSV3d - rs111033439 Germline - 0/96 controls none - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+?/? 53 c.10585G>A r.(?) p.(Gly3529Ser) Fibronectin type-III 20 (3499-3585) Unknown ACMG VUS g.215956080C>T g.215782738C>T - - USH2A_000431 Heterozygous; unknown PubMed: McGee 2010, USMA missense analysis, missense variant in MSV3d - rs111033439 Germline - - none - - DNA SEQ - - USH2 - PubMed: McGee 2010 Proband - No genotype in the publication - - United States - - - - - 1 Anne-Françoise Roux
+?/. 53 c.10585G>A r.(?) p.(Gly3529Ser) - Unknown - likely pathogenic g.215956080C>T - p.G3529S - USH2A_000431 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
+?/. 53 c.10585G>A r.(?) p.(Gly3529Ser) - Parent #2 - likely pathogenic g.215956080C>T - c.10585G>A - USH2A_000431 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - F - - - - - - - 1 Daan Panneman
?/. - c.10585G>A r.(?) p.(Gly3529Ser) - Unknown ACMG VUS g.215956080C>T g.215782738C>T - - USH2A_000431 ACMG GN005 criteria: PM2_P PM3_M PubMed: Le Quesne Stabej, P. et al., 2012; PubMed: Wafa, T. T. et al., 2021 - rs111033439 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.