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     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
-/. - c.785-16_785-15del r.(=) p.(=) - Unknown - benign g.216501011_216501012del g.216327669_216327670del USH2A(NM_206933.4):c.785-16_785-15delAT - USH2A_000539 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/? 04i c.785-16_785-15del r.(=) p.(=) - Maternal (confirmed) ACMG likely benign g.216501011_216501012del g.216327669_216327670del 785-16_785-15delAT - USH2A_000539 Heterozygous; UV1 PubMed: Le Quesne Stabej 2012 - - Germline - 0/878 controls +HpyCH4IV;+PmlI;+BsaAI;-NlaIII;-FatI;-PciI; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/? 04i c.785-16_785-15del r.= p.= - Unknown ACMG likely benign g.216501011_216501012del g.216327669_216327670del 785-16_785-15delAT - USH2A_000539 Heterozygous; RT-PCR on hair roots cells showed normal sequence; Presumed non-pathogenic PubMed: Nakanishi 2011 - - Germline - 1/270 +HpyCH4IV;+PmlI;+BsaAI;-NlaIII;-FatI;-PciI; - - RNA RT-PCR, SEQ - - USH2 - PubMed: Nakanishi 2011 Proband - No genotype in the publication - - Japan - - - - - 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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