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     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/+ 63 c.12708T>A r.(?) p.(Cys4236*) Fibronectin type-III 27 (4154-4258) Paternal (inferred) - pathogenic g.215848545A>T g.215675203A>T - - USH2A_000531 Homozygous; Probable pathogenic PubMed: Nakanishi 2011 - - Germline - 0/220 controls none - - DNA SEQ - - USH2 - PubMed: Nakanishi 2011 Proband F - Japan - - - - - 1 Anne-Françoise Roux
+/+ 63 c.12708T>A r.(?) p.(Cys4236*) Fibronectin type-III 27 (4154-4258) Maternal (inferred) - pathogenic g.215848545A>T g.215675203A>T - - USH2A_000531 Homozygous; Probable pathogenic PubMed: Nakanishi 2011 - - Germline - 0/220 controls none - - DNA SEQ - - USH2 - PubMed: Nakanishi 2011 Proband F - Japan - - - - - 1 Anne-Françoise Roux
+?/. - c.12708T>A r.(?) p.(Cys4236*) - Unknown ACMG pathogenic g.215848545A>T - - - USH2A_000531 - - - - Germline/De novo (untested) - - - - - DNA SEQ-NG-I - - RP IR_GS_0024 - - F - Korea, South (Republic) - - - - - 1 Jinu Han
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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