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     
+?/. - c.2792G>A r.(?) p.(Cys931Tyr) - Unknown - likely pathogenic g.216144001G>T g.215970659G>T c.2792C>T, p.(Cys931Tyr) - USH2A_002063 error in annotation: c.2792C>T instead of G>A , compound heterozygous PubMed: Wang 2019 - - Germline ? - - - - DNA SEQ-NG blood panel of 126 genes retinal disease 13720 PubMed: Wang 2019 - M - China - - - - - 1 LOVD
+?/. - c.6923C>A r.(?) p.(Ala2308Glu) - Unknown - likely pathogenic (recessive) g.216144001G>T g.215970659G>T - - USH2A_002063 - PubMed: Xu 2014 - - Germline - 1/314 case chromosomes - - - DNA SEQ - - retinal disease RP300 PubMed: Xu 2014 - - - China - - - - - 1 Isabelle Audo
+?/. 36 c.6923C>A r.(?) p.(Ala2308Glu) - Parent #1 ACMG likely pathogenic g.216144001G>T g.215970659G>T USH2A c.6923C>A, p.A2308E - USH2A_002063 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease 43861981 PubMed: Zhu 2021 family 111, patient 43861981 F - China - - - - - 1 LOVD
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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