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.

5 entries on 1 page. Showing entries 1 - 5.
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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.14792-2A>G r.spl p.? - Unknown - pathogenic g.215814078T>C g.215640736T>C - - USH2A_002006 - PubMed: Ge 2015 - - Germline - - - - - DNA SEQ-NG - 195-gene panel retinal disease VHM+Y.45 PubMed: Ge 2015 simplex case - - United States - - - - - 1 LOVD
+?/+ - c.14792-2A>G r.spl? p.? - Unknown ACMG VUS g.215814078T>C - - - USH2A_002006 - - - - Germline/De novo (untested) - - - - - DNA SEQ-NG-I - - RP IR_GH_0188 - - M - Korea, South (Republic) - - - - - 1 Jinu Han
+?/. 67i c.14792-2A>G r.spl? p.? - Unknown - likely pathogenic g.215814078T>C - c.14792–2A>G - USH2A_002006 - PubMed: Song-2011 - - Unknown - - - - - DNA arraySEQ, PCR blood - retinal disease - PubMed: Song-2011 - F - - - - - - - 1 LOVD
+?/. 67i c.14792-2A>G r.spl? p.? - Unknown - likely pathogenic g.215814078T>C - c.14792-2A>G - USH2A_002006 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
+/. - c.14792-2A>G r.spl p.? - Unknown ACMG pathogenic g.215814078T>C g.215640736T>C - - USH2A_002006 ACMG GN005 criteria: PVS1_VS PM2_P PM3_P PubMed: Wafa, T. T. et al., 2021 - rs137853923 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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