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)     

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ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

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Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

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VIP     

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Panel size     

Owner     
+/+ 65 c.14175G>A r.(?) p.(Trp4725*) Fibronectin type-III 32 (4633-4730) Parent #2 - pathogenic g.215824102C>T g.215650760C>T - - USH2A_000671 Heterozygous; Pathogenic PubMed: Garcia-Garcia 2011 - - Germline - - -PflMI;-BslI; - - DNA SEQ - - USH - PubMed: Garcia-Garcia 2011 Proband - - Spain - - - - - 1 Jose Maria Millan
+/+ 65 c.14175G>A r.(?) p.(Trp4725*) Fibronectin type-III 32 (4633-4730) Parent #1 - pathogenic g.215824102C>T g.215650760C>T - - USH2A_000671 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband F - France - - - - - 1 Crystel Bonnet
+/. 65 c.14175G>A r.(?) p.(Trp4725*) - Parent #2 - pathogenic g.215824102C>T - c.14175G>A - USH2A_000671 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - F - - - - - - - 1 Daan Panneman
+/. - c.14175G>A r.(?) p.(Trp4725Ter) - Unknown ACMG pathogenic g.215824102C>T g.215650760C>T - - USH2A_000671 ACMG GN005 criteria: PVS1_VS PM2_P PM3_M PubMed: Garcia-Garcia, G. et al., 2011 - rs886042722 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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