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.9740-1G>A r.(?) p.(?) - Unknown - likely pathogenic g.215972468C>T g.215799126C>T - - USH2A_001730 - - - - Unknown - - - - - DNA SEQ - - ? - - - F - (Germany) - - - - - 1 IMGAG
+/. - c.9740-1G>A r.spl p.? - Unknown ACMG pathogenic g.215972468C>T g.215799126C>T USH2A c.9740-1G>A, . - USH2A_001730 marked as causative, heterozygous PubMed: Ma 2021 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ - whole exome sequencing retinal disease 60 PubMed: Ma 2021 - ? - Korea - - - - - 1 LOVD
+/. - c.9740-1G>A r.spl p.? - Unknown ACMG pathogenic g.215972468C>T g.215799126C>T - - USH2A_001730 ACMG GN005 criteria: PVS1_VS PS1_S PM2_P PubMed: Ma, D. J. et al., 2021 - rs1662239185 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.9740-1G>A r.spl p.? - Unknown ACMG pathogenic (recessive) g.215972468C>T g.215799126C>T - - USH2A_001730 ACMG PM2, PVS1_STRONG, PP5_STRONG PubMed: Weisschuh 2024 - - Germline - - - - - DNA SEQ-NG - WGS ? ARRP-443 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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