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.

6 entries on 1 page. Showing entries 1 - 6.
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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     
+?/. 63 c.12575G>A r.(?) p.(Arg4192His) - Unknown - likely pathogenic g.215848678C>T g.215675336C>T - - USH2A_001126 - Sharon, submitted - - Germline - - - - - DNA SEQ - - retinal disease - Sharon, submitted - M no Israel Jewish-Ashkenazi - - - - 2 Dror Sharon
+?/. 63 c.12575G>A r.(?) p.(Arg4192His) - Unknown - likely pathogenic g.215848678C>T g.215675336C>T - - USH2A_001126 - Sharon, submitted - - Germline - - - - - DNA SEQ - - retinal disease - Sharon, submitted - F no Israel Jewish-Ashkenazi - - - - 1 Dror Sharon
+?/. 63 c.12575G>A r.(?) p.(Arg4192His) - Unknown - likely pathogenic g.215848678C>T g.215675336C>T - - USH2A_001126 - Sharon, submitted - - Germline - - - - - DNA SEQ - - retinal disease - Sharon, submitted - M no Israel Jewish-Ashkenazi - - - - 1 Dror Sharon
+?/. 63 c.12575G>A r.(?) p.(Arg4192His) - Both (homozygous) - likely pathogenic g.215848678C>T g.215675336C>T - - USH2A_001126 - PubMed: Kimchi 2018 - - Germline - - - - - DNA SEQ - - retinal disease MOL0897 PubMed: Kimchi 2018 - M no Israel Jewish-Ashkenazi - - - - 2 Dror Sharon
+?/. 63 c.12575G>A r.(?) p.(Arg4192His) - Unknown - likely pathogenic g.215848678C>T g.215675336C>T - - USH2A_001126 - Sharon, submitted - - Germline - - - - - DNA SEQ - - retinal disease - Sharon, submitted - M no Israel Jewish - - - - 1 Dror Sharon
+?/. 63 c.12575G>A r.(?) p.(Arg4192His) - Unknown - likely pathogenic g.215848678C>T g.215675336C>T - - USH2A_001126 - Sharon, submitted - - Germline - - - - - DNA SEQ - - retinal disease - Sharon, submitted - F no Israel Jewish-Ashkenazi - - - - 1 Dror Sharon
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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