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.

4 entries on 1 page. Showing entries 1 - 4.
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     
+/+ 38i c.7301-1G>A r.spl p.? - Unknown - pathogenic g.216074248C>T g.215900906C>T - - USH2A_000761 Heterozygous; likely pathogenic PubMed: Glöckle 2014 - - Germline - - -AluI;-CviKI_1; - - DNA SEQ, SEQ-NG-S - - RPar - PubMed: Glöckle 2014 Proband - - - - - - - - 1 Anne-Françoise Roux
+?/. - c.7301-1G>A r.(?) p.(?) - Parent #1 - likely pathogenic g.216074248C>T g.215900906C>T USH2A, variant 1: c.7301-1G>A/p.?, variant 2: c.6902T>C/p.L2301S - USH2A_000761 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET3 targeted sequencing panel - see paper retinal disease 195 PubMed: Weisschuh 2020 Filing key number: 72, sporadic retinitis pigmentosa, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
+?/. - c.7301-1G>A r.spl p.(?) - Parent #1 - likely pathogenic g.216074248C>T g.215900906C>T USH2A, variant 1: c.6713A>C/p.E2238A, variant 2: c.7301-1G>A/p.? - USH2A_000761 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET1 targeted sequencing panel - see paper retinal disease 517 PubMed: Weisschuh 2020 Filing key number: 172, Usher syndrome type 2, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
+?/. - c.7301-1G>A r.spl p.? - Unknown ACMG likely pathogenic g.216074248C>T g.215900906C>T - - USH2A_000761 ACMG GN005 criteria: PVS1_VS PM2_P PubMed: Glockle, N. et al., 2014; PubMed: Weisschuh, N. et al., 2020 - rs1438496892 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.