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     
+/. 21i c.4627+2T>C r.spl? p.? - Unknown - pathogenic g.216348592A>G - c.4627+2T>C - USH2A_002154 - PubMed: Fu-2013 - - Germline - - - - - DNA SEQ-NG blood - retinal disease - PubMed: Fu-2013 - M - China Chinese - - - - 2 LOVD
+/. 21i c.4627+2T>C r.spl p.(?) - Parent #2 ACMG pathogenic g.216348592A>G g.216175250A>G USH2A c.4627+2T>C - USH2A_002154 - PubMed: Zhu 2021 - - Germline yes - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease 16999034 PubMed: Zhu 2021 family 16*, patient 16999034 M - China - - - - - 1 LOVD
+/. 21i c.4627+2T>C r.spl p.(?) - Parent #2 ACMG pathogenic g.216348592A>G g.216175250A>G USH2A c.4627+2T>C - USH2A_002154 - PubMed: Zhu 2021 - - Germline yes - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease 16999034_1 PubMed: Zhu 2021 family 16*, patient 16999034_1 F - China - - - - - 1 LOVD
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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