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.6001C>T r.(?) p.(Arg2001Cys) - Unknown - VUS g.216243491G>A g.216070149G>A USH2A(NM_206933.4):c.6001C>T (p.R2001C) - USH2A_001629 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.6001C>T r.(?) p.(Arg2001Cys) - Unknown - likely pathogenic (recessive) g.216243491G>A g.216070149G>A - - USH2A_001629 - PubMed: Xu 2014 - rs141539554 Germline - 2/314 case chromosomes - - - DNA SEQ-NG - gene panel retinal disease RP301 PubMed: Xu 2014 - - - China - - - - - 1 LOVD
+?/. - c.6001C>T r.(?) p.(Arg2001Cys) - Unknown - likely pathogenic (recessive) g.216243491G>A g.216070149G>A - - USH2A_001629 - PubMed: Xu 2014 - rs141539554 Germline - 2/314 case chromosomes - - - DNA SEQ-NG - gene panel retinal disease RP296 PubMed: Xu 2014 family M - China - - - - - 1 LOVD
-/. 30 c.6001C>T r.(6001c>u) p.(Arg2001Cys) - Parent #1 ACMG benign g.216243491G>A g.216070149G>A - - USH2A_001629 no variant 2nd chromome PubMed: Reurink 2023, Journal: Reurink 2023 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease arRP30 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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