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.

3 entries on 1 page. Showing entries 1 - 3.
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.10403C>T r.(?) p.(Pro3468Leu) - Parent #2 - likely pathogenic g.215956262G>A g.215782920G>A - - USH2A_001952 - PubMed: Bravo-Gil 2017 - - Germline - - - - - DNA SEQ-NG - 68-gene panel retinal disease Pat108 PubMed: Bravo-Gil 2017 patient - - Spain - - - - - 1 Nereida Bravo Gil
+?/. 53 c.10403C>T r.(?) p.(Pro3468Leu) - Parent #2 ACMG likely pathogenic g.215956262G>A g.215782920G>A USH2A c.10403C>T, p.P3468L - USH2A_001952 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease SRF_1748 PubMed: Zhu 2021 family 51, patient SRF_1748 F - China - - - - - 1 LOVD
?/. - c.10403C>T r.(?) p.(Pro3468Leu) - Unknown ACMG VUS g.215956262G>A g.215782920G>A - - USH2A_001952 ACMG GN005 criteria: PM2_P PM3_P PubMed: Bravo-Gil, N. et al., 2017 - rs1553261476 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.