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.
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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     
+/. - c.3883C>T r.(?) p.(Arg1295Ter) - Unknown - pathogenic g.216371855G>A g.216198513G>A - - USH2A_000166 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/+ 18 c.3883C>T r.(?) p.(Arg1295*) Fibronectin type-III 3 (1242-1357) Parent #2 - pathogenic g.216371855G>A g.216198513G>A - - USH2A_000166 Heterozygous PubMed: Dreyer 2000 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Dreyer 2000 Proband - - Norway - - - - - 1 Anne-Françoise Roux
+/+ 18 c.3883C>T r.(?) p.(Arg1295*) Fibronectin type-III 3 (1242-1357) Parent #1 - pathogenic g.216371855G>A g.216198513G>A - - USH2A_000166 Heterozygous PubMed: Weston 2000 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Weston 2000 Proband - - Sweden - - - - - 1 Anne-Françoise Roux
+/+ 18 c.3883C>T r.(?) p.(Arg1295*) Fibronectin type-III 3 (1242-1357) Parent #2 - pathogenic g.216371855G>A g.216198513G>A - - USH2A_000166 Heterozygous PubMed: Jaijo 2010 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Jaijo 2010 Proband M - Spain - - - - - 1 Jose Maria Millan
+/. - c.3883C>T r.(?) p.(Arg1295*) - Parent #1 - pathogenic g.216371855G>A g.216198513G>A USH2A c.3883C>T, p.Arg1295* - USH2A_000166 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing USH RD17091313 PubMed: Gao 2021 - M - China - - - - - 1 LOVD
+/. - c.3883C>T r.(?) p.(Arg1295Ter) - Unknown ACMG pathogenic g.216371855G>A g.216198513G>A - - USH2A_000166 ACMG GN005 criteria: PVS1_VS PM2_P PM3_P PubMed: Gao, F. J. et al., 2021; PubMed: Garcia-Garcia, G. et al., 2011 - rs764797292 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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