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.662C>A r.(?) p.(Thr221Lys) - Parent #2 - likely pathogenic g.216538417G>T g.216365075G>T - - USH2A_001882 - PubMed: Maeda 2018 - - Germline - - - - - DNA SEQ, SEQ-NG - 39-gene panel retinal disease Pat28 PubMed: Maeda 2018 patient, no family history F - Japan - - - - - 1 LOVD
+?/. - c.662C>A r.(?) p.(Thr221Lys) - Parent #1 - likely pathogenic g.216538417G>T g.216365075G>T USH2A c.662C>A, p.(Thr221Lys) - USH2A_001882 heterozygous PubMed: Inaba 2020 - - Unknown ? - - - - DNA SEQ-NG-I - panel of 39 (238 patients) or 50 (287 patients) genes retinal disease - PubMed: Inaba 2020 - - - Japan - - - - - 1 LOVD
?/. - c.662C>A r.(?) p.(Thr221Lys) - Unknown ACMG VUS g.216538417G>T g.216365075G>T - - USH2A_001882 ACMG GN005 criteria: PM2_P PubMed: Inaba, A. et al., 2020 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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