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.

6 entries on 1 page. Showing entries 1 - 6.
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     
+/+ 26 c.5189_5199del r.(?) p.(Tyr1730Trpfs*6) Laminin G-like 2 (1714-1891) Maternal (confirmed) - pathogenic g.216256900_216256910del g.216083558_216083568del - - USH2A_000351 Heterozygous PubMed: Baux 2014 - - Germline - - +NcoI;+BsaJI;+BtgI;+StyI; - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband F - France - - - - - 1 Anne-Françoise Roux
+/+ 26 c.5189_5199del r.(?) p.(Tyr1730Trpfs*6) Laminin G-like 2 (1714-1891) Parent #1 - pathogenic g.216256900_216256910del g.216083558_216083568del - - USH2A_000351 Heterozygous; Pathogenic PubMed: Bonnet 2011 - - Germline - - +NcoI;+BsaJI;+BtgI;+StyI; - - DNA SEQ - - USH3 - PubMed: Bonnet 2011 Proband - - - - - - - - 1 Anne-Françoise Roux
+/+ 26 c.5189_5199del r.(?) p.(Tyr1730Trpfs*6) Laminin G-like 2 (1714-1891) Paternal (confirmed) - pathogenic g.216256900_216256910del g.216083558_216083568del - - USH2A_000351 Homozygous; Pathogenic PubMed: Lenarduzzi 2015 - - Germline - - +NcoI;+BsaJI;+BtgI;+StyI; - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Lenarduzzi 2015 Proband - - Italy - - - - - 1 Anne-Françoise Roux
+/+ 26 c.5189_5199del r.(?) p.(Tyr1730Trpfs*6) Laminin G-like 2 (1714-1891) Maternal (confirmed) - pathogenic g.216256900_216256910del g.216083558_216083568del - - USH2A_000351 Homozygous; Pathogenic PubMed: Lenarduzzi 2015 - - Germline - - +NcoI;+BsaJI;+BtgI;+StyI; - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Lenarduzzi 2015 Proband - - Italy - - - - - 1 Anne-Françoise Roux
+/. 26 c.5189_5199del r.(?) p.(Tyr1730Trpfs*6) - Both (homozygous) - pathogenic g.216256897_216256907del - c.5189_5199del - USH2A_000351 - PubMed: Colombo-2020 - - Germline yes - - - - DNA SEQ - - retinal disease - PubMed: Colombo-2020 - F no - - - - - - 1 LOVD
+/. - c.5189_5199del r.(?) p.(Tyr1730TrpfsTer6) - Unknown ACMG pathogenic g.216256900_216256910del g.216083558_216083568del - - USH2A_000351 ACMG GN005 criteria: PVS1_VS PM2_P PM3_P PubMed: Colombo, L. et al., 2022 - - 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.