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     
+/+ 68 c.14911C>T r.(?) p.(Arg4971*) Fibronectin type-III 35 (4928-5014) Unknown - pathogenic g.215813957G>A g.215640615G>A - - USH2A_000552 Heterozygous; Pathogenic PubMed: Le Quesne Stabej 2012 - - Germline - - +Tsp45I;+HphI;-Hpy99I; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/+ 68 c.14911C>T r.(?) p.(Arg4971*) Fibronectin type-III 35 (4928-5014) Parent #2 - pathogenic g.215813957G>A g.215640615G>A - - USH2A_000552 Heterozygous; mutation PubMed: Jiang 2015 - - Germline - - +Tsp45I;+HphI;-Hpy99I; - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Jiang 2015 Proband M - China - - - - - 1 Anne-Françoise Roux
+/. - c.14911C>T r.(?) p.(Arg4971*) - Unknown ACMG pathogenic g.215813957G>A g.215640615G>A USH2A c.14911C>T, p.(Arg4971*), c.3407G>A, p.(Ser1136Asn) - USH2A_000552 - PubMed: Jespersgaar 2019 - - Germline ? - - - - DNA SEQ-NG-I blood 125 genes associated with inherited retinal disorders, see paper supplemental data retinal disease 280 PubMed: Jespersgaar 2019 - ? - Denmark - - - - - 1 LOVD
+?/. - c.14911C>T r.(?) p.(Arg4971*) - Unknown - likely pathogenic g.215813957G>A g.215640615G>A c.2299delG p.(Glu767Serfs*21), c.14911C>T p.(Arg4971*) - USH2A_000552 - PubMed: Hagag 2020 - - Germline/De novo (untested) ? - - - - DNA ? - - retinal disease Subject 041 PubMed: Hagag 2020 - ? - - - - - - - 1 LOVD
+/. - c.14911C>T r.(?) p.(Arg4971Ter) - Unknown ACMG pathogenic g.215813957G>A g.215640615G>A USH2A c.C14911T, p.R4971X - USH2A_000552 marked as causative, heterozygous PubMed: Ma 2021 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ - whole exome sequencing retinal disease 135 PubMed: Ma 2021 - ? - Korea - - - - - 1 LOVD
+?/. - c.14911C>T r.(?) p.(Arg4971*) - Parent #1 - likely pathogenic g.215813957G>A g.215640615G>A USH2A c.14911C>T - USH2A_000552 protein variant annotation not written; heterozygous PubMed: Toms 2020 - - Unknown ? - - - - ? ? - retrospective cohort retinal disease 6 PubMed: Toms 2020 - ? - United Kingdom (Great Britain) - - - - - 1 LOVD
+/. 68 c.14911C>T r.(?) p.(Arg4971*) - Parent #2 ACMG pathogenic g.215813957G>A g.215640615G>A USH2A c.14911C>T, p.R4971* - USH2A_000552 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease USHsrf7 PubMed: Zhu 2021 family 192, patient USHsrf7 M - China - - - - - 1 LOVD
+/. - c.14911C>T r.(?) p.(Arg4971Ter) - Unknown ACMG pathogenic g.215813957G>A g.215640615G>A - - USH2A_000552 ACMG GN005 criteria: PVS1_VS PM2_P PM3 PubMed: Ma, D. J. et al., 2021; PubMed: Le Quesne Stabej, P. et al., 2012; PubMed: Jiang, L. et al., 2015; PubMed: Toms, M. et al., 2020 - rs397517994 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.