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     
+/. - c.9882C>G r.(?) p.(Cys3294Trp) - Unknown - pathogenic (recessive) g.215972325G>C - 1:215972325G>C ENST00000307340.3:c.9882C>G (Cys3294Trp) - USH2A_001811 - PubMed: Carss 2017 - - Germline - - - - - DNA SEQ-NG - WES retinal disease B240075 PubMed: Carss 2017 - F - United Kingdom (Great Britain) - - - - - 1 LOVD
+/. - c.9882C>G r.(?) p.(Cys3294Trp) - Parent #2 - pathogenic g.215972325G>C g.215798983G>C - - USH2A_001811 - PubMed: Biswas 2017 - rs749228276 Germline - - - - - DNA SEQ-NG - WES retinal disease RF.SH.0008 PubMed: Biswas 2017 - - - United States white - - - - 1 LOVD
+/. - c.9882C>G r.(?) p.(Cys3294Trp) - Parent #1 - pathogenic (recessive) g.215972325G>C g.215798983G>C - - USH2A_001811 - PubMed: Consugar 2015 - - Germline yes - - - - DNA SEQ-NG - 238-gene panel retinal disease OGI-388-841 PubMed: Consugar 2015 - - - United States - - - - - 1 LOVD
+/. 50 c.9882C>G r.(?) p.(Cys3294Trp) - Unknown - pathogenic g.215972325G>C - c.9882C>G - USH2A_001811 - PubMed: Nishiguchi-2013 - - Germline - - - - - DNA SEQ-NG blood - retinal disease - PubMed: Nishiguchi-2013 - F no - Mixed European - - - - 1 Julia Lopez
+?/. 50 c.9882C>G r.(?) p.(Cys3294Trp) - Parent #1 - likely pathogenic g.215972325G>C - c.9882C>G - USH2A_001811 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - M - - - - - - - 1 Daan Panneman
+?/. 50 c.9882C>G r.(?) p.(Cys3294Trp) - Parent #1 - likely pathogenic g.215972325G>C - c.9882C>G - USH2A_001811 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - F - - - - - - - 1 Daan Panneman
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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