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.

3 entries on 1 page. Showing entries 1 - 3.
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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     
+/+ 41 c.8141G>A r.(?) p.(Trp2714*) Fibronectin type-III 13 (2621-2718) Unknown - pathogenic g.216061850C>T g.215888508C>T - - USH2A_000827 Heterozygous PubMed: Baux 2014 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband M - - - - - - - 1 Anne-Françoise Roux
+/. 41 c.8141G>A r.(?) p.(Trp2714*) - Parent #2 ACMG pathogenic (recessive) g.216061850C>T - - - USH2A_000827 - - - - Germline yes - - - - DNA SEQ-NG-I - Exome sequencing USH Pat28 PubMed: Bahena 2021 - M no Mexico - - - - - 1 Barbara Vona
+/. - c.8141G>A r.(?) p.(Trp2714Ter) - Unknown ACMG pathogenic g.216061850C>T g.215888508C>T - - USH2A_000827 ACMG GN005 criteria: PVS1_VS PM2_P PM3_P PubMed: Bahena, P. et al., 2022 - rs1238086961 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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