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     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/+ 20 c.4354dup r.(?) p.(Cys1452Leufs*25) Fibronectin type-III 4 (1367-1462) Unknown - pathogenic g.216363608dup g.216190266dup - - USH2A_000569 Heterozygous; Pathogenic PubMed: Le Quesne Stabej 2012 - - Germline - - none - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/+ 20 c.4354dup r.(?) p.(Cys1452Leufs*25) Fibronectin type-III 4 (1367-1462) Paternal (inferred) - pathogenic g.216363608dup g.216190266dup - - USH2A_000569 Homozygous; Pathogenic PubMed: Le Quesne Stabej 2012 - - Germline - - none - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/+ 20 c.4354dup r.(?) p.(Cys1452Leufs*25) Fibronectin type-III 4 (1367-1462) Maternal (inferred) - pathogenic g.216363608dup g.216190266dup - - USH2A_000569 Homozygous; Pathogenic PubMed: Le Quesne Stabej 2012 - - Germline - - none - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/. - c.4354dup r.(?) p.(Cys1452LeufsTer25) - Unknown ACMG pathogenic g.216363608dup g.216190266dup 4354dupT - USH2A_000569 ACMG GN005 criteria: PVS1_VS PM2_P PM3_P PubMed: Le Quesne Stabej, P. et al., 2012 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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