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.

7 entries on 1 page. Showing entries 1 - 7.
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     
+?/? 8 c.1390C>T r.(?) p.(Arg464Cys) Laminin N-terminal (271-517) Unknown ACMG VUS g.216496976G>A g.216323634G>A - - USH2A_000221 Heterozygous PubMed: Seyedahmadi 2004, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Seyedahmadi 2004 Proband - - United States - - - - - 1 Anne-Françoise Roux
+?/. - c.1390C>T r.(?) p.(Arg464Cys) - Parent #1 - likely pathogenic g.216496976G>A g.216323634G>A - - USH2A_000221 - PubMed: Stone 2017 - - Germline - - - - - DNA SEQ-NG - - retinal disease 101 PubMed: Stone 2017 1 affected F - (United States) - - - - - 1 LOVD
+?/. - c.1390C>T r.(?) p.(Arg464Cys) - Unknown ACMG likely pathogenic g.216496976G>A g.216323634G>A USH2A:NM_206933 c.C1390T, p.R464C - USH2A_000221 heterozygous, individual solved, variant causal PubMed: Rodriguez-Munoz 2020 - - Germline ? - - - - DNA SEQ-NG-I blood - retinal disease RPN-288 PubMed: Rodriguez-Munoz 2020 family fRPN-131, proband F - Spain - - - - - 1 LOVD
+?/. - c.1390C>T r.(?) p.(Arg464Cys) - Unknown ACMG likely pathogenic g.216496976G>A g.216323634G>A USH2A:NM_206933 c.C1390T, p.R464C - USH2A_000221 heterozygous, individual solved, variant causal PubMed: Rodriguez-Munoz 2020 - - Germline yes - - - - DNA SEQ-NG-I blood - retinal disease RPN-525 PubMed: Rodriguez-Munoz 2020 family fRPN-224, proband F - Spain - - - - - 1 LOVD
+?/. - c.1390C>T r.(?) p.(Arg464Cys) - Unknown - likely pathogenic g.216496976G>A g.216323634G>A c.1390C>T, p.Arg464Cys - USH2A_000221 heterozygous PubMed: Zampaglione 2020 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ blood - retinal disease 003-071 PubMed: Zampaglione 2020 - ? - - - - - - - 1 LOVD
+?/. - c.1390C>T r.(?) p.(Arg464Cys) - Parent #1 - likely pathogenic g.216496976G>A g.216323634G>A USH2A, variant 1: c.1390C>T/p.R464C, variant 2: c.8782G>T/p.G2928* - USH2A_000221 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET3 targeted sequencing panel - see paper retinal disease 1107 PubMed: Weisschuh 2020 Filing key number: 747, sporadic retinitis pigmentosa, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
?/. - c.1390C>T r.(?) p.(Arg464Cys) - Unknown ACMG VUS g.216496976G>A g.216323634G>A - - USH2A_000221 ACMG GN005 criteria: PM2_P PM3_P PubMed: Rodriguez-Munoz, A. et al., 2020; PubMed: Weisschuh, N. et al., 2020 - rs1423536179 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.