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     
+/+ 52 c.10272_10274dup r.(?) p.(Cys3425Phefs*4) Fibronectin type-III 19 (3404-3494) Parent #1 - pathogenic g.215960125_215960127dup g.215786783_215786785dup - - USH2A_000177 Heterozygous PubMed: Jaijo 2010 - - Germline - - - - - DNA SEQ, SSCA - - USH2 - PubMed: Jaijo 2010 Proband - - Spain - - - - - 1 Jose Maria Millan
+/+ 52 c.10272_10274dup r.(?) p.(Cys3425Phefs*4) Fibronectin type-III 19 (3404-3494) Parent #2 - pathogenic g.215960125_215960127dup g.215786783_215786785dup - - USH2A_000177 Heterozygous PubMed: Najera 2002 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Najera 2002 Proband M - Spain - - - - - 1 Jose Maria Millan
+/+ 52 c.10272_10274dup r.(?) p.(Cys3425Phefs*4) Fibronectin type-III 19 (3404-3494) Parent #2 - pathogenic g.215960125_215960127dup g.215786783_215786785dup - - USH2A_000177 Heterozygous PubMed: Aller 2006 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Aller 2006 Relative F - Spain - - - - - 1 Jose Maria Millan
+/+ 52 c.10272_10274dup r.(?) p.(Cys3425Phefs*4) Fibronectin type-III 19 (3404-3494) Parent #2 - pathogenic g.215960125_215960127dup g.215786783_215786785dup - - USH2A_000177 Heterozygous PubMed: Aller 2006 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Aller 2006 Relative F - Spain - - - - - 1 Jose Maria Millan
+/. - c.10272_10274dup r.(?) p.(Cys3425Phefs*4) - Parent #2 - pathogenic g.215960125_215960127dup g.215786783_215786785dup C3425Ffs*4 - USH2A_000177 - PubMed: Sanchez-Alcudia 2014 - - Germline - - - - - DNA SEQ - - retinal disease RP-0184PatVI6 PubMed: Sanchez-Alcudia 2014 multi-generation family, at least 12 affected, complex inheriatnce of several diseases M - Spain - - - - - 12 LOVD
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.