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.

4 entries on 1 page. Showing entries 1 - 4.
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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     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/+ 36 c.6931del r.(?) p.(Ala2311Profs*15) Fibronectin type-III 9 (2241-2325) Unknown - pathogenic g.216143994del g.215970652del 6931delG - USH2A_000092 Heterozygous PubMed: Baux 2007 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Baux 2007 Proband M - France - - - - - 1 Anne-Françoise Roux
+/+ 36 c.6931del r.(?) p.(Ala2311Profs*15) Fibronectin type-III 9 (2241-2325) Unknown - pathogenic g.216143994del g.215970652del 6931delG - USH2A_000092 Heterozygous PubMed: Baux 2014 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband M - France - - - - - 1 Anne-Françoise Roux
+?/. - c.6931del r.(?) p.(Ala2311Profs*15) - Parent #1 - likely pathogenic g.216143994del g.215970652del USH2A c.6931del, p.A231PfsX15 - USH2A_000092 error in annotation: p.A231PfsX15 should be p.A2311PfsX15, compound heterozygous PubMed: Jauregui 2020 - - Unknown ? - - - - DNA SEQ-NG blood targeted sequencing retinal disease 127 PubMed: Jauregui 2020 - M - (United States) Hispanic - - - - 1 LOVD
+?/. - c.6931del r.(?) p.(Ala2311ProfsTer15) - Unknown ACMG likely pathogenic g.216143994del g.215970652del 6931delG - USH2A_000092 ACMG GN005 criteria: PVS1_VS PM2_P PubMed: Ganapathi, M. et al., 2022; PubMed: Jauregui, R. et al., 2020 - rs1667471296 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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