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     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/+ 4-1 c.672_1840+1160del r.spl p.? Laminin N-terminal (271-517);Laminin EGF-like 1 (518-574);Laminin EGF-like 2 (575-640) Unknown - pathogenic g.216464359_216538409del g.216291017_216365067del hg19:chr1:g.216464357_216538407del - USH2A_000903 Heterozygous PubMed: Dad 2015, PubMed: Dad 2016 - - Germline - - - - - DNA MLPA - - USH2 55555;USH2-8 (D69) PubMed: Dad 2015, PubMed: Dad 2016 Proband F - - - - - - - 1 Shzeena Dad
+/+ 4-1 c.672_1840+1160del r.spl p.? Laminin N-terminal (271-517);Laminin EGF-like 1 (518-574);Laminin EGF-like 2 (575-640) Parent #2 - pathogenic g.216464359_216538409del g.216291017_216365067del hg19:chr1:g.216464357_216538407del - USH2A_000903 Heterozygous PubMed: Dad 2015, PubMed: Dad 2016 - - Germline - - - - - DNA MLPA, SEQ - - USH2 70353;USH2-7 PubMed: Dad 2015, PubMed: Dad 2016 Proband M - - - - - - - 1 Shzeena Dad
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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