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     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/. 60 c.11683G>T r.(11683g>u) p.(Gly3895*) - Parent #1 ACMG pathogenic g.215914745C>A g.215741403C>A - - USH2A_002107 - Journal: Reurink 2021 - - Germline no - - - - DNA SEQ-NG - gene panel retinal disease W19-0921 Journal: Reurink 2021 - - - - - - - - - 1 Janine Reurink
+/. - c.11683G>T r.(?) p.(Gly3895*) - Parent #1 ACMG pathogenic g.215914745C>A g.215741403C>A USH2A c.11683G>T, p.(Gly3895*) - USH2A_002107 heterozygous PubMed: Reurink 2021 - - Unknown ? - - - - DNA SEQ-NG-I - molecular inversion probe-based sequencing retinal disease W19-0921 PubMed: Reurink 2021 genetically unexplained subjects from centers in the Netherlands, Ireland and Poland ? - Netherlands - - - - - 1 LOVD
+/. - c.11683G>T r.(?) p.(Gly3895Ter) - Unknown ACMG pathogenic g.215914745C>A g.215741403C>A - - USH2A_002107 ACMG GN005 criteria: PVS1_VS PM2_P PM3_P PubMed: Reurink, J. et al., 2021 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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