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.1823G>A r.(?) p.(Cys608Tyr) - Unknown ACMG VUS g.216465534C>T g.216292192C>T USH2A c.1823G>A, p.C608Y - USH2A_002589 heterozygous PubMed: Lee 2020 - - Germline yes - - - - DNA SEQ-NG-I blood Whole exome sequencing USH SB237-461 PubMed: Lee 2020 - M - Korea - - - - - 1 LOVD
+?/. 10 c.1823G>A r.(1823g>a) p.(Cys608Tyr) - Parent #1 ACMG likely pathogenic g.216465534C>T g.216292192C>T - - USH2A_002589 - PubMed: de Bruijn 2023, PubMed: Reurink 2023, Journal: Reurink 2023 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease 071364;USH8 PubMed: de Bruijn 2023, PubMed: Reurink 2023, Journal: Reurink 2023 - - - - - - - - - 1 Janine Reurink
?/. - c.1823G>A r.(?) p.(Cys608Tyr) - Unknown ACMG VUS g.216465534C>T g.216292192C>T - - USH2A_002589 ACMG GN005 criteria: PM2_P PM3_P PP3_P PubMed: Dad, S. et al., 2015 - rs1475577009 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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