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     
+/+ 26i c.5298+1G>C r.5168_5271del p.Gly1723Glufs*6 Laminin G-like 2 (1714-1891) Parent #1 - pathogenic g.216256797C>G g.216083455C>G - - USH2A_000173 Heterozygous; E26 skipping (Jaijo , 2010) PubMed: Aller 2006 - - Germline - 0/100 controls - - - DNA minigene, SEQ - - USH2 - PubMed: Aller 2006 Proband F - Spain - - - - - 1 Jose Maria Millan
+?/. 26i c.5298+1G>C r.spl? p.(?) - Parent #1 - likely pathogenic g.216256797C>G - c.5298+1G>C - USH2A_000173 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - M - - - - - - - 1 Daan Panneman
+?/. - c.5298+1G>C r.spl p.? - Unknown ACMG likely pathogenic g.216256797C>G g.216083455C>G - - USH2A_000173 ACMG GN005 criteria: PVS1_VS PM2_P PubMed: Aller, E. et al., 2006 - - 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.