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)     

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.1571C>T r.(?) p.(Ala524Val) - Unknown - VUS g.216495298G>A g.216321956G>A - - USH2A_001672 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.1571C>T r.(?) p.(Ala524Val) - Parent #1 ACMG likely pathogenic (recessive) g.216495298G>A - - - USH2A_001672 - PubMed: Bahena 2021 - - Germline yes - - - - DNA SEQ-NG-I - Exome sequencing USH2A Pat21 PubMed: Bahena 2021 - F yes Iran - - - - - 1 Barbara Vona
+?/. 9 c.1571C>T r.(?) p.(Ala524Val) - Unknown - likely pathogenic g.216495298G>A g.216321956G>A USH2A Ex.9 c.1571C>T p.(Ala524Val), Ex.50 c.9804T>A p.(Cys3268*) - USH2A_001672 compound heterozygous PubMed: Martin Merida 2019 - - Germline/De novo (untested) ? - - - - DNA SEQ-NG-I - - retinal disease RP-1696 PubMed: Martin Merida 2019 - ? - Spain - - - - - 1 LOVD
?/. - c.1571C>T r.(?) p.(Ala524Val) - Unknown ACMG VUS g.216495298G>A g.216321956G>A - - USH2A_001672 ACMG GN005 criteria: PM2_P PM3_P PubMed: Bahena, P. et al., 2022 - rs772624410 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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