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     
+/. - c.10636G>T r.(?) p.(Gly3546*) - Parent #2 ACMG pathogenic (recessive) g.215955488C>A g.215782146C>A - - USH2A_001846 - PubMed: Sun 2018 - - Germline - - - - - DNA SEQ - - HL 19578 PubMed: Sun 2018 sporadic case - no China - - - - - 1 LOVD
+/. 54 c.10636G>T r.(?) p.(Gly3546*) - Parent #1 - pathogenic g.215955488C>A - c.10636G>T - USH2A_001846 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - F - - - - - - - 1 Daan Panneman
+/. - c.10636G>T r.(?) p.(Gly3546Ter) - Unknown ACMG pathogenic g.215955488C>A g.215782146C>A - - USH2A_001846 ACMG GN005 criteria: PVS1_VS PM2_P PM3_M PubMed: Sun, T. et al., 2018 - rs1553261372 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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