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.

5 entries on 1 page. Showing entries 1 - 5.
Legend   How to query  

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     
+?/. 37 c.6986C>A r.(?) p.(Pro2329His) - Unknown - likely pathogenic g.462946C>A g.215965451G>T c.6986C>A, p.P2329H - USH2A_002241 compound heterozygous PubMed: Liu 2020 - - Unknown ? - - - - DNA SEQ-NG, SEQ blood - retinal disease RP04-II:2 PubMed: Liu 2020 - F no - - - - - - 1 LOVD
?/. - c.6986C>A r.(?) p.(Pro2329His) - Unknown ACMG VUS g.216138793G>T g.215965451G>T USH2A c.C6986A, p.P2329H - USH2A_002241 marked as causative, heterozygous PubMed: Ma 2021 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ - whole exome sequencing retinal disease 131 PubMed: Ma 2021 - ? - Korea - - - - - 1 LOVD
+?/. 37 c.6986C>A r.(?) p.(Pro2329His) - Unknown - likely pathogenic (recessive) g.216138793G>T - c.6986C>A - USH2A_002241 - PubMed: Liu-2020 - - Germline - - - - - DNA SEQ-NG - hereditary eye disease enrichment panel (HEDEP) retinal disease - PubMed: Liu-2020 - F - - - - - - - 1 LOVD
+?/. 37 c.6986C>A r.(?) p.(Pro2329His) - Parent #1 ACMG likely pathogenic g.216138793G>T g.215965451G>T USH2A c.6986C>A, p.P2329H - USH2A_002241 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease SRF578 PubMed: Zhu 2021 family 106, patient SRF578 M - China - - - - - 1 LOVD
?/. - c.6986C>A r.(?) p.(Pro2329His) - Unknown ACMG VUS g.216138793G>T g.215965451G>T - - USH2A_002241 ACMG GN005 criteria: PM2_P PM3_P PP3_P PubMed: Ma, D. J. et al., 2021 - rs554957414 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
Legend   How to query  

All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.