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.

2 entries on 1 page. Showing entries 1 - 2.
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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     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
?/. 54 c.10588C>A r.(?) p.(Pro3530Thr) - Unknown ACMG VUS g.215955536G>T g.215782194G>T USH2A c.10588C>A, p.(Pro3530Thr) - USH2A_002232 heterozygous PubMed: Dan 2020 - - Germline yes - - - - DNA SEQ-NG blood Panel 6 containing 386 genes retinal disease 173 PubMed: Dan 2020 - M no China - - - - - 1 LOVD
?/. - c.10588C>A r.(?) p.(Pro3530Thr) - Unknown ACMG VUS g.215955536G>T g.215782194G>T - - USH2A_002232 ACMG GN005 criteria: PM2_P BP4_P PubMed: Dan, H. et al., 2020 - rs1298379123 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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