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     
+/. - c.486-1G>C r.spl p.? - Both (homozygous) - pathogenic g.216592022C>G g.216418680C>G - - USH2A_002037 - PubMed: Neuhaus 2017 - - Germline - - - - - DNA SEQ-NG - gene panel USH Pat89 PubMed: Neuhaus 2017 - - yes Saudi Arabia - - - - - 1 LOVD
+/. - c.486-1G>C r.spl p.? - Both (homozygous) - pathogenic g.216592022C>G g.216418680C>G - - USH2A_002037 - PubMed: Neuhaus 2017 - - Germline - - - - - DNA SEQ-NG - gene panel USH Pat118 PubMed: Neuhaus 2017 - - yes Saudi Arabia - - - - - 1 LOVD
+/. - c.486-1G>C r.spl p.(?) - Unknown - pathogenic g.216592022C>G g.216418680C>G USH2A c.486-1G>C - USH2A_002037 heterozygous PubMed: Zampaglione 2020 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ blood - retinal disease OGI602_001240 PubMed: Zampaglione 2020 - ? - - - - - - - 1 LOVD
+?/. - c.486-1G>C r.spl p.(?) - Both (homozygous) - likely pathogenic g.216592022C>G g.216418680C>G USH2A c.486-1G>C - USH2A_002037 homozygous PubMed: Méjécase 2020 - - Unknown ? - - - - DNA SEQ-NG - retrospective case note review, targeted gene panel testing retinal disease 40 {PMID:Méjécase 2020:3278337 - ? - United Arab Emirates - - - - - 1 LOVD
+?/. - c.486-1G>C r.spl p.(?) - Both (homozygous) - likely pathogenic g.216592022C>G g.216418680C>G USH2A c.486-1G>C - USH2A_002037 homozygous PubMed: Méjécase 2020 - - Unknown ? - - - - DNA SEQ-NG - retrospective case note review, targeted gene panel testing retinal disease 41 {PMID:Méjécase 2020:3278337 - ? - United Arab Emirates - - - - - 1 LOVD
Legend   How to query  

All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.