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     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+?/. - c.8710G>A r.(?) p.(Val2904Ile) - Unknown - likely pathogenic (recessive) g.216040484C>T g.215867142C>T - - USH2A_002058 - PubMed: Xu 2014 - rs142649882 Germline - 1/314 case chromosomes - - - DNA PCR, SEQ, SEQ-NG blood WES retinal disease RP387_II:1 PubMed: Xu 2014 index case M no China Asia - - - - 2 Manon Peeters
?/. 44 c.8710G>A r.(8710g>a) p.(Val2904Ile) - Parent #1 ACMG VUS g.216040484C>T g.215867142C>T - - USH2A_002058 no variant 2nd chromome PubMed: Reurink 2023, Journal: Reurink 2023 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease arRP47 PubMed: Reurink 2023, Journal: Reurink 2023 - - - - - - - - - 1 Janine Reurink
?/. - c.8710G>A r.(?) p.(Val2904Ile) - Unknown ACMG VUS g.216040484C>T g.215867142C>T - - USH2A_002058 ACMG PM2 PubMed: Weisschuh 2024 - - Germline - - - - - DNA SEQ-NG - WGS ? USHII-361 PubMed: Weisschuh 2024 patient, no family history F - Germany - - - - - 1 Johan den Dunnen
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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