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     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/. - c.922_923insGCCA r.(?) p.(His308Argfs*16) - Unknown - pathogenic (recessive) g.216498867_216498868insTGGC - 1:216498866G>GTGGC ENST00000307340.3:c.920_923dupGCCA (His308GlnfsTer16) - USH2A_001830 - PubMed: Carss 2017 - - Germline - - - - - DNA SEQ-NG - WES retinal disease B240007 PubMed: Carss 2017 - M - United Kingdom (Great Britain) - - - - - 1 LOVD
+/. - c.922_923insGCCA r.(?) p.(His308Argfs*16) - Unknown - pathogenic (recessive) g.216498867_216498868insTGGC - 1:216498866G>GTGGC ENST00000307340.3:c.920_923dupGCCA (His308GlnfsTer16) - USH2A_001830 - PubMed: Carss 2017 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease G000985 PubMed: Carss 2017 - M - United Kingdom (Great Britain) Europe - - - - 1 LOVD
+?/. - c.922_923insGCCA r.(?) p.(His308Argfs*16) - Unknown - likely pathogenic (recessive) g.216498867_216498868insTGGC - 1:216498866G>GTGGC ENST00000307340.3:c.920_923dupGCCA (His308GlnfsTer16) - USH2A_001830 - PubMed: Carss 2017 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease G005258 PubMed: Carss 2017 - F - United Kingdom (Great Britain) Europe - - - - 1 LOVD
+/. - c.922_923insGCCA r.(?) p.(His308Argfs*16) - Unknown - pathogenic (recessive) g.216498867_216498868insTGGC - 1:216498866G>GTGGC ENST00000307340.3:c.920_923dupGCCA (His308GlnfsTer16) - USH2A_001830 - PubMed: Carss 2017 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease G007683 PubMed: Carss 2017 - F - United Kingdom (Great Britain) Europe - - - - 1 LOVD
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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