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     
+/+ 17 c.3788G>A r.(?) p.(Trp1263*) Fibronectin type-III 3 (1242-1357) Maternal (confirmed) - pathogenic g.216372992C>T g.216199650C>T - - USH2A_000745 Heterozygous; Disease causing PubMed: Xu 2011 - - Germline - 0/200 controls -BsaI - - DNA PCRdig, SEQ - - USH2 - PubMed: Xu 2011 Proband M - China - - - - - 1 Anne-Françoise Roux
+/. - c.3788G>A r.(?) p.(Trp1263*) - Parent #1 ACMG pathogenic (recessive) g.216372992C>T g.216199650C>T - - USH2A_000745 - PubMed: Sun 2018 - - Germline - - - - - DNA SEQ - - HL 19082 PubMed: Sun 2018 sporadic case - no China - - - - - 1 LOVD
+/. 17 c.3788G>A r.(?) p.(Trp1263*) - Unknown ACMG pathogenic g.216372992C>T g.216199650C>T NM_206933.2:c.3788G>A, NP_996816.2:p.(Trp1263Ter), NC_000001.10:g.216372992C>T - USH2A_000745 - PubMed: Wang 2018 - - Germline ? - - - - DNA SEQ-NG - exome sequencing retinal disease 2016101007 PubMed: Wang 2018 - M ? China Han Chinese - - - - 1 LOVD
+?/. 17 c.3788G>A r.(?) p.(Trp1263*) - Unknown - likely pathogenic (recessive) g.216372992C>T - c.3788G>A - USH2A_000745 - PubMed: Liu-2020 - - Germline - - - - - DNA SEQ-NG - WES retinal disease - PubMed: Liu-2020 - M - - - - - - - 1 LOVD
+/. - c.3788G>A r.(?) p.(Trp1263*) - Parent #2 - pathogenic g.216372992C>T g.216199650C>T USH2A c.3788G>A, p.Trp1263* - USH2A_000745 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing USH RD17080296 PubMed: Gao 2021 - M - China - - - - - 1 LOVD
+/. - c.3788G>A r.(?) p.(Trp1263*) - Parent #2 - pathogenic g.216372992C>T g.216199650C>T USH2A c.3788G>A, p.Trp1263* - USH2A_000745 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing USH RD18021256 PubMed: Gao 2021 - M - China - - - - - 1 LOVD
+/. - c.3788G>A r.(?) p.(Trp1263*) - Parent #2 - pathogenic g.216372992C>T g.216199650C>T USH2A c.3788G>A, p.Trp1263* - USH2A_000745 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing retinal disease RD18070019 PubMed: Gao 2021 - F - China - - - - - 1 LOVD
+/. - c.3788G>A r.(?) p.(Trp1263*) - Parent #2 - pathogenic g.216372992C>T g.216199650C>T USH2A c.3788G>A, p.Trp1263* - USH2A_000745 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing retinal disease RD18070019 PubMed: Gao 2021 - F - China - - - - - 1 LOVD
+/. 17 c.3788G>A r.(?) p.(Trp1263*) - Parent #2 ACMG pathogenic g.216372992C>T g.216199650C>T USH2A c.3788G>A, p.W1263* - USH2A_000745 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease AXLM_31 PubMed: Zhu 2021 family 156, patient AXLM_31 M - China - - - - - 1 LOVD
+/. - c.3788G>A r.(?) p.(Trp1263Ter) - Unknown ACMG pathogenic g.216372992C>T g.216199650C>T - - USH2A_000745 ACMG GN005 criteria: PVS1_VS PM2_P PM3_M PP1_P PubMed: Gao, F. J. et al., 2021; PubMed: Sun, T. et al., 2018 - rs1572042090 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.