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     
+?/. 10 c.1751G>T r.(?) p.(Cys584Phe) - Paternal (confirmed) - likely pathogenic g.216465606C>A g.216292264C>A - - USH2A_000858 - PubMed: de Castro-Miró 2014 - - Germline yes - - - - DNA SEQ-NG-I Whole blood - USH2A - PubMed: de Castro-Miró 2014 - F no Spain - - - - - 1 Marta de Castro-Miró
+?/? 10 c.1751G>T r.(?) p.(Cys584Phe) Laminin EGF-like 2 (575-640) Parent #1 ACMG VUS g.216465606C>A g.216292264C>A - - USH2A_000858 Heterozygous; mutation PubMed: de Castro-Miro 2014, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA PE, SEQ - APEX USH2 - PubMed: de Castro-Miro 2014 Proband F - Spain - - - - - 1 Anne-Françoise Roux
+?/? 10 c.1751G>T r.(?) p.(Cys584Phe) Laminin EGF-like 2 (575-640) Parent #1 ACMG VUS g.216465606C>A g.216292264C>A - - USH2A_000858 Heterozygous; mutation PubMed: de Castro-Miro 2014, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ - - USH2 - PubMed: de Castro-Miro 2014 Relative M - Spain - - - - - 1 Anne-Françoise Roux
+?/. 10 c.1751G>T r.(?) p.(Cys584Phe) - Unknown - likely pathogenic g.216465606C>A - c.1751G>T - USH2A_000858 - PubMed: de Castro-Miró-2014 - - Germline - - - - - DNA PE - - retinal disease 40ORG PubMed: de Castro-Miró-2014 - - - - - - - - - 2 LOVD
+?/. - c.1751G>T r.(?) p.(Cys584Phe) - Maternal (confirmed) ACMG likely pathogenic g.216465606C>A - - - USH2A_000858 - PubMed: Mansard et al, 2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - USH2A - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
+?/. 10 c.1751G>T r.(?) p.(Cys584Phe) - Unknown - likely pathogenic (recessive) g.216465606C>A - c.1751G>T - USH2A_000858 - PubMed: Colombo-2020 - - Germline yes - - - - DNA SEQ - - retinal disease - PubMed: Colombo-2020 - M no - - - - - - 1 LOVD
+?/. - c.1751G>T r.(?) p.(Cys584Phe) - Unknown ACMG likely pathogenic g.216465606C>A g.216292264C>A - - USH2A_000858 ACMG GN005 criteria: PM2_P PM3_S PP3_P PubMed: Colombo, L. et al., 2022; PubMed: Mansard, L. et al., 2021; PubMed: Colombo, L. et al., 2021 - rs2037016118 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.