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     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/+ 12 c.2073C>A r.(?) p.(Cys691*) Laminin EGF-like 3 (641-693) Parent #1 - pathogenic g.216424339G>T g.216250997G>T - - USH2A_000213 Heterozygous PubMed: Seyedahmadi 2004 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Seyedahmadi 2004 Proband - Genotype deduced from Sandberg et al., 2008 - - United States - - - - - 1 Anne-Françoise Roux
+/. - c.2073C>A r.(?) p.(Cys691*) - Parent #1 - pathogenic g.216424339G>T g.216250997G>T - - USH2A_000213 - PubMed: Neuhaus 2017 - - Germline - - - - - DNA SEQ-NG - gene panel USH Pat8 PubMed: Neuhaus 2017 - - no Germany - - - - - 1 LOVD
+/. - c.2073C>A r.(?) p.(Cys691Ter) - Unknown ACMG pathogenic g.216424339G>T g.216250997G>T - - USH2A_000213 ACMG GN005 criteria: PVS1_VS PM2_P PM3_P PubMed: Neuhaus, C. et al., 2017 - rs376674482 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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