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.
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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.10931C>T r.(?) p.(Thr3644Met) - Unknown - VUS g.215953193G>A g.215779851G>A - - USH2A_001973 - PubMed: Tiwari 2016 - - Germline - - - - - DNA SEQ-NG - WES retinal disease Case71808 PubMed: Tiwari 2016 see paper M - Switzerland - - - - - 1 LOVD
?/. 55 c.10931C>T r.(?) p.(Thr3644Met) - Both (homozygous) - VUS g.215953193G>A g.215779851G>A C10931T - USH2A_001973 - PubMed: Katagiri 2014 - rs185823130 Germline - - - - - DNA SEQ-NG - WES retinal disease RP#028 PubMed: Katagiri 2014 family - - Japan - - - - - 1 LOVD
+?/. 55 c.10931C>T r.(?) p.(Thr3644Met) - Unknown - likely pathogenic (recessive) g.215953193G>A - c.10931C>T - USH2A_001973 - PubMed: Liu-2020 - - Germline - - - - - DNA SEQ-NG - hereditary eye disease enrichment panel (HEDEP) retinal disease - PubMed: Liu-2020 - M - - - - - - - 1 LOVD
?/. 55 c.10931C>T r.(10931c>u) p.(Thr3644Met) - Parent #1 ACMG VUS g.215953193G>A g.215779851G>A - - USH2A_001973 - PubMed: Reurink 2023, Journal: Reurink 2023 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease arRP7 PubMed: Reurink 2023, Journal: Reurink 2023 - - - - - - - - - 1 Janine Reurink
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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