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     
-/? 40 c.7525C>T r.(?) p.(Arg2509Trp) Fibronectin type-III 11 (2435-2528) Unknown ACMG likely benign g.216073486G>A g.215900144G>A - - USH2A_000699 Heterozygous PubMed: Baux 2014, USMA missense analysis, missense variant in MSV3d - - Germline - - none - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband M - France - - - - - 1 Anne-Françoise Roux
?/. - c.7525C>T r.(?) p.(Arg2509Trp) - Unknown - VUS g.216073486G>A g.215900144G>A - - USH2A_000699 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 - - Germline - 1/1204 cases with retinitis pigmentosa - - - DNA SEQ-NG - - retinal disease - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - 1 Yoshito Koyanagi
?/. - c.7525C>T r.(?) p.(Arg2509Trp) - Both (homozygous) - VUS g.216073486G>A g.215900144G>A - - USH2A_000699 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 - - Germline - 1/1204 cases with retinitis pigmentosa - - - DNA SEQ-NG - - retinal disease - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - 1 Yoshito Koyanagi
+?/. - c.7525C>T r.(?) p.(Arg2509Trp) - Parent #1 - likely pathogenic g.216073486G>A g.215900144G>A - - USH2A_000699 - PubMed: Bravo-Gil 2017 - - Germline - - - - - DNA SEQ-NG - 68-gene panel retinal disease Pat71 PubMed: Bravo-Gil 2017 patient - - Spain - - - - - 1 Nereida Bravo Gil
+/. - c.7525C>T r.(?) p.(Arg2509Trp) - Parent #2 - pathogenic g.216073486G>A g.215900144G>A USH2A c.7525C>T, p.Arg2509Trp - USH2A_000699 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing USH RD180430A PubMed: Gao 2021 - M - China - - - - - 1 LOVD
?/. - c.7525C>T r.(?) p.(Arg2509Trp) - Unknown ACMG VUS g.216073486G>A g.215900144G>A - - USH2A_000699 ACMG GN005 criteria: PM2_P PM3_M PubMed: Gao, F. J. et al., 2021; PubMed: Bravo-Gil, N. et al., 2017 - rs1394948601 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.