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.

10 entries on 1 page. Showing entries 1 - 10.
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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.11549-5del r.spl? p.? - Unknown - benign g.215914895del g.215741553del - - USH2A_001340 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.11549-5del r.(=) p.(=) - Unknown - VUS g.215914895del g.215741553del c.115495delT - USH2A_001340 - PubMed: Xu 2014 - rs34565443 Germline - 7/314 case chromosomes - - - DNA SEQ-NG - gene panel retinal disease RP215 PubMed: Xu 2014 family F - China - - - - - 1 LOVD
?/. - c.11549-5del r.(=) p.(=) - Unknown - VUS g.215914895del g.215741553del c.11549-5delT - USH2A_001340 - PubMed: Xu 2014 - rs34565443 Germline - 7/314 case chromosomes - - - DNA SEQ-NG - gene panel retinal disease RP288 PubMed: Xu 2014 family M - China - - - - - 1 LOVD
?/. - c.11549-5del r.(=) p.(=) - Unknown - VUS g.215914895del g.215741553del c.11549-5delT - USH2A_001340 - PubMed: Xu 2014 - rs34565443 Germline - 7/314 case chromosomes - - - DNA SEQ-NG - gene panel retinal disease RP331 PubMed: Xu 2014 patient M - China - - - - - 1 LOVD
?/. - c.11549-5del r.(=) p.(=) - Unknown - VUS g.215914895del g.215741553del c.11549-5delT - USH2A_001340 - PubMed: Xu 2014 - rs34565443 Germline - 7/314 case chromosomes - - - DNA SEQ-NG - gene panel retinal disease RP031 PubMed: Xu 2014 - - - China - - - - - 1 LOVD
?/. - c.11549-5del r.(=) p.(=) - Unknown - VUS g.215914895del g.215741553del c.11549-5delT - USH2A_001340 - PubMed: Xu 2014 - rs34565443 Germline - 7/314 case chromosomes - - - DNA SEQ-NG - gene panel retinal disease RP240 PubMed: Xu 2014 - - - China - - - - - 1 LOVD
?/. - c.11549-5del r.(=) p.(=) - Unknown - VUS g.215914895del g.215741553del c.11549-5delT - USH2A_001340 - PubMed: Xu 2014 - rs34565443 Germline - 7/314 case chromosomes - - - DNA SEQ-NG - gene panel retinal disease RP275 PubMed: Xu 2014 patient F - China - - - - - 1 LOVD
?/. - c.11549-5del r.(=) p.(=) - Unknown - VUS g.215914895del g.215741553del c.11549-5delT - USH2A_001340 - PubMed: Xu 2014 - rs34565443 Germline - 7/314 case chromosomes - - - DNA SEQ-NG - gene panel retinal disease RP396 PubMed: Xu 2014 family M - China - - - - - 1 LOVD
+?/. - c.11549-5del r.spl? p.(?) - Parent #2 - likely pathogenic g.215914895del g.215741553del USH2A c.11549-5delT, - - USH2A_001340 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing retinal disease RD18050819 PubMed: Gao 2021 - M - China - - - - - 1 LOVD
-/. - c.11549-5del r.(?) p.(=) - Unknown ACMG benign g.215914895del g.215741553del 11549-5delT - USH2A_001340 ACMG GN005 criteria: BA1 BS2_S BP4_P PubMed: Gao, F. J. et al., 2021 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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