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     
+/. 46 c.9119G>A r.(?) p.(Trp3040*) - Unknown ACMG pathogenic g.216017775C>T g.215844433C>T - - USH2A_001123 - PubMed: de Castro-Miró 2016 - - Germline yes - - - - DNA SEQ-NG-I Whole blood - USH2A 79ORG1 PubMed: de Castro-Miró 2016 - F no Uganda - - - - - 1 Marta de Castro-Miró
+?/. - c.9119G>A r.(?) p.(Trp3040*) - Parent #2 - likely pathogenic (recessive) g.216017775C>T g.215844433C>T - - USH2A_001123 - PubMed: Fuster-Garcia 2018 - - Germline - - - - - DNA arraySEQ - - retinal disease RP1906t PubMed: Fuster-Garcia 2018 analysis 77 USH patients - - Spain - - - - - 1 Global Variome, with Curator vacancy
+/. - c.9119G>A r.(?) p.(Trp3040*) - Unknown ACMG pathogenic g.216017775C>T g.215844433C>T USH2A c.9119G>A (p.Trp3040*) - USH2A_001123 heterozygous PubMed: Dineiro 2020 - - Germline ? - - - - DNA SEQ-NG-I, SEQ blood, saliva targeted sequencing with 1 of 4 panels of OFTALMOgenics probes retinal disease OFTALMO.077 PubMed: Dineiro 2020 - ? - Spain - - - - - 1 LOVD
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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