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     
-?/? 3 c.488G>A r.(?) p.(Cys163Tyr) - Unknown ACMG likely benign g.216592019C>T g.216418677C>T - - USH2A_000023 Heterozygous PubMed: Dreyer 2000, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Dreyer 2000 Proband - - Denmark - - - - - 1 Anne-Françoise Roux
+?/. - c.488G>A r.(?) p.(Cys163Tyr) - Unknown - likely pathogenic g.216592019C>T g.216418677C>T - - USH2A_000023 - PubMed: Huang 2018 - - Germline - - - - - DNA SEQ-NG - 283-gene panel retinal disease RP014 PubMed: Huang 2018 - - - - - - - - - 1 LOVD
+/. 12 c.488G>A r.(?) p.(Cys163Tyr) - Parent #2 - pathogenic (recessive) g.216592019C>T g.216418677C>T - - USH2A_000023 possible duplicate PubMed: Dreyer 2000, PubMed: Dreyer 2008, Tranebjaerg 2011, PubMed: Dad 2016 - - Germline - - - - - DNA SEQ - - retinal disease USH2-13 (D21) PubMed: Dreyer 2000, PubMed: Dreyer 2008, Tranebjaerg 2011, PubMed: Dad 2016 family, 2 affeted F no Denmark - - - - - 2 Anne-Françoise Roux
+/. 12 c.488G>A r.(?) p.(Cys163Tyr) - Parent #2 - pathogenic (recessive) g.216592019C>T g.216418677C>T - - USH2A_000023 possible duplicate PubMed: Dreyer 2000, PubMed: Dreyer 2008, Tranebjaerg 2011, PubMed: Dad 2016 - - Germline - - - - - DNA SEQ - - retinal disease USH2-13a PubMed: Dreyer 2000, PubMed: Dreyer 2008, Tranebjaerg 2011, PubMed: Dad 2016 - M no Denmark - - - - - 1 Anne-Françoise Roux
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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