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.

2 entries on 1 page. Showing entries 1 - 2.
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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     

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VIP     

Data_av     

Treatment     

Panel size     

Owner     
+?/? 63 c.12302_12304del r.(?) p.(Asn4101del) Fibronectin type-III 26 (4066-4150) Parent #2 ACMG VUS g.215848952_215848954del g.215675610_215675612del 12302_12304delACA - USH2A_001036 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
?/. - c.12302_12304del r.(?) p.(Asn4101del) - Unknown ACMG VUS g.215848952_215848954del g.215675610_215675612del 12302_12304delACA - USH2A_001036 ACMG GN005 criteria: PM2_P PM3_M PM4_M PubMed: Bonnet, C. et al., 2016; PubMed: Mansard, L. et al., 2021 - rs1657997491 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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