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.

8 entries on 1 page. Showing entries 1 - 8.
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     
+/+ 6 c.956G>A r.(?) p.(Cys319Tyr) Laminin N-terminal (271-517) Paternal (inferred) - pathogenic g.216498834C>T g.216325492C>T - - USH2A_000207 Homozygous PubMed: Weston 2000, USMA missense analysis, missense variant in MSV3d - rs121912599 Germline - 0/190 controls - - - DNA SEQ - - USH2 - PubMed: Weston 2000 Proband - - United States - - - - - 1 Anne-Françoise Roux
+/+ 6 c.956G>A r.(?) p.(Cys319Tyr) Laminin N-terminal (271-517) Maternal (inferred) - pathogenic g.216498834C>T g.216325492C>T - - USH2A_000207 Homozygous PubMed: Weston 2000, USMA missense analysis, missense variant in MSV3d - rs121912599 Germline - 0/190 controls - - - DNA SEQ - - USH2 - PubMed: Weston 2000 Proband - - United States - - - - - 1 Anne-Françoise Roux
+?/. 6 c.956G>A r.(?) p.(Cys319Tyr) - Unknown - likely pathogenic g.216498834C>T - c.956G>A,p.C319Y - USH2A_000207 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
+/. - c.956G>A r.(?) p.(Cys319Tyr) - Both (homozygous) ACMG pathogenic g.216498834C>T - - - USH2A_000207 - Villafuerte-de la Cruz RA, et al., 2023. Submitted ClinVar-39614 rs121912599 Germline yes - - - - DNA SEQ-NG-I BUCCAL SWAB - retinitis pigmentosa, X-linked, and sinorespiratory infections, with/without deafness 2947207 Villafuerte-de la Cruz RA, et al., 2023. Submitted - F no Mexico Hispanic - - - none 1 Rocio Villafuerte-de la Cruz
+/. - c.956G>A r.(?) p.(Cys319Tyr) - Unknown ACMG pathogenic g.216498834C>T g.216325492C>T - - USH2A_000207 - Villafuerte-de la Cruz RA, et al., 2023. Submitted ClinVar-2355 rs121912599 Germline yes - - - - DNA SEQ-NG-I Buccal swab - USH2A 2638009 Villafuerte-de la Cruz RA, et al., 2023. Submitted - M no Mexico Hispanic - - - None 1 Rocio Villafuerte-de la Cruz
+/. - c.956G>A r.(?) p.(Cys319Tyr) - Unknown ACMG pathogenic g.216498834C>T g.216325492C>T - - USH2A_000207 - Villafuerte-de la Cruz RA, et al., 2023. Submitted ClinVar-2355 rs121912599 Germline yes - - - - DNA SEQ-NG-I - - USH2A 2746846 Villafuerte-de la Cruz RA, et al., 2023. Submitted - M no Mexico Hispanic - - - NONE 1 Rocio Villafuerte-de la Cruz
+/. - c.956G>A r.(?) p.(Cys319Tyr) - Unknown ACMG pathogenic g.216498834C>T g.216325492C>T - - USH2A_000207 - Villafuerte-de la Cruz RA, et al., 2023. Submitted ClinVar-2355 rs121912599 Germline - - - - - DNA SEQ-NG-I - - USH2A 3022893 Villafuerte-de la Cruz RA, et al., 2023. Submitted - M no Mexico Hispanic - - - NONE 1 Rocio Villafuerte-de la Cruz
?/. - c.956G>A r.(?) p.(Cys319Tyr) - Unknown ACMG VUS g.216498834C>T g.216325492C>T - - USH2A_000207 ACMG GN005 criteria: PM2_P PubMed: Sloan-Heggen, C. M. et al., 2016 - rs121912599 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.