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.

10 entries on 1 page. Showing entries 1 - 10.
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     
+/+ 13 c.2431_2432del r.(?) p.(Lys811Aspfs*11) Laminin EGF-like 6 (795-846) Parent #1 - pathogenic g.216420304_216420305del g.216246962_216246963del 2431_2432delAA - USH2A_000196 Heterozygous PubMed: Jaijo 2010 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Jaijo 2010 Proband F - Spain - - - - - 1 Jose Maria Millan
+/+ 13 c.2431_2432del r.(?) p.(Lys811Aspfs*11) Laminin EGF-like 6 (795-846) Parent #2 - pathogenic g.216420304_216420305del g.216246962_216246963del 2431_2432delAA - USH2A_000196 Heterozygous PubMed: Najera 2002 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Najera 2002 Proband M - Spain - - - - - 1 Jose Maria Millan
+/+ 13 c.2431_2432del r.(?) p.(Lys811Aspfs*11) Laminin EGF-like 6 (795-846) Parent #1 - pathogenic g.216420304_216420305del g.216246962_216246963del 2431_2432delAA - USH2A_000196 Heterozygous PubMed: Bernal 2005 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Bernal 2005 Proband M - Spain - - - - - 1 Anne-Françoise Roux
+/+ 13 c.2431_2432del r.(?) p.(Lys811Aspfs*11) Laminin EGF-like 6 (795-846) Parent #1 - pathogenic g.216420304_216420305del g.216246962_216246963del 2431_2432delAA - USH2A_000196 Heterozygous PubMed: Bernal 2005 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Bernal 2005 Relative F - Spain - - - - - 1 Anne-Françoise Roux
+/+ 13 c.2431_2432del r.(?) p.(Lys811Aspfs*11) Laminin EGF-like 6 (795-846) Parent #2 - pathogenic g.216420304_216420305del g.216246962_216246963del 2431_2432delAA - USH2A_000196 Heterozygous PubMed: Bernal 2005 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Bernal 2005 Proband M - Spain - - - - - 1 Anne-Françoise Roux
+?/. - c.2431_2432del r.(?) p.(Lys811Aspfs*11) - Unknown - likely pathogenic g.216420304_216420305del g.216246962_216246963del - - USH2A_000196 USH2A-caused RP; additional test revealed CNGB3 homozygous mutation which was causative of achromatopsia in the same patient PubMed: Perez-Carro 2018 - - Germline yes - - - - DNA arraySNP blood - retinal disease RP-0605b PubMed: Perez-Carro 2018 family RP-0605b M yes Spain - - - - - 1 LOVD
+?/. - c.2431_2432del r.(?) p.(Lys811Aspfs*11) - Paternal (confirmed) - likely pathogenic g.216420304_216420305del g.216246962_216246963del - - USH2A_000196 - PubMed: Perez-Carro 2018 - - Germline yes - - - - DNA arraySNP blood - retinal disease RP-0610 PubMed: Perez-Carro 2018 family RP-0610 F no Spain - - - - - 1 LOVD
+?/. - c.2431_2432del r.(?) p.(Lys811Aspfs*11) - Paternal (confirmed) - likely pathogenic g.216420304_216420305del g.216246962_216246963del - - USH2A_000196 - PubMed: Perez-Carro 2018 - - Germline yes - - - - DNA arraySNP blood - retinal disease RP-1817 PubMed: Perez-Carro 2018 family RP-1817 M no Spain - - - - - 1 LOVD
+?/. 13 c.2431_2432del r.(?) p.(Lys811Aspfs*11) - Unknown - likely pathogenic g.216420304_216420305del g.216246962_216246963del USH2A Ex.13 c.2276G>T p.(Cys759Phe), Ex.13 c.2431_2432del p.(Lys811fs*11) - USH2A_000196 compound heterozygous PubMed: Martin Merida 2019 - - Germline yes - - - - DNA SEQ-NG-I - - retinal disease RP-1817 PubMed: Martin Merida 2019 - ? - Spain - - - - - 1 LOVD
+/. - c.2431_2432del r.(?) p.(Lys811AspfsTer11) - Unknown ACMG pathogenic g.216420304_216420305del g.216246962_216246963del 2431_2432delAA - USH2A_000196 ACMG GN005 criteria: PVS1_VS PM2_P PM3_S PubMed: Perez-Carro, R. et al., 2018 - rs2102545818 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.