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.
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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     
+?/. 39 c.7364G>A r.(?) p.(Trp2455*) - Unknown - likely pathogenic g.216074184C>T g.215900842C>T - - USH2A_001125 - PubMed: de Castro-Miró 2014 - - Germline - - - - - DNA SEQ-NG-I Whole blood - retinal disease - PubMed: de Castro-Miró 2014 - M no Reunion - - - - - 1 Marta de Castro-Miró
+?/. 39 c.7364G>A r.(?) p.(Trp2455*) - Paternal (confirmed) - likely pathogenic g.216074184C>T g.215900842C>T - - USH2A_001125 - PubMed: de Castro-Miró et al. 2014 - - Germline - - - - - DNA SEQ-NG-I Whole blood - retinal disease - PubMed: de Castro-Miró 2014 - M no Spain - - - - - 1 Marta de Castro-Miró
+?/. 39 c.7364G>A r.(?) p.(Trp2455*) - Unknown - likely pathogenic g.216074184C>T - c.7364G>A - USH2A_001125 - PubMed: de Castro-Miró-2014 - - Germline - - - - - DNA SEQ-NG - WES retinal disease E5 PubMed: de Castro-Miró-2014 - - - - - - - - - 1 LOVD
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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