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     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
?/. - c.3158-2A>G r.spl p.? - Unknown - VUS g.216380775T>C g.216207433T>C - - USH2A_001980 - PubMed: Ellingford 2016 - - Germline - - - - - DNA SEQ - 105-gene panel retinal disease 13008753 PubMed: Ellingford 2016 patient - - - - - - - - 1 LOVD
+?/. - c.3158-2A>G r.(?) p.(?) - Parent #2 - likely pathogenic g.216380775T>C g.216207433T>C USH2A c.31582A>G, p.(?) - USH2A_001980 heterozygous PubMed: Molina-Ramirez 2020 - - Unknown ? - - - - DNA SEQ-NG-I - 14 patients: 105-gene panel, 13 samples: 176-gene panel using previously described method (O', Sullivan J et al. 2012) USH 13008753 PubMed: Molina-Ramirez 2020 - F - United Kingdom (Great Britain) - - - - - 1 LOVD
+/. - c.3158-2A>G r.spl p.? - Unknown ACMG pathogenic g.216380775T>C g.216207433T>C - - USH2A_001980 ACMG GN005 criteria: PVS1_VS PM2_P PM3_P PubMed: Molina-Ramirez, L. P. et al., 2020 - rs878853404 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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