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     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
?/. 54 c.10601A>G r.(?) p.(Tyr3534Cys) - Unknown ACMG VUS g.215782181T>C g.215782181T>C USH2A c.10601A > G, p.Tyr3534Cys, heterozygous - USH2A_002245 - PubMed: Sun 2020 - - Unknown ? - - - - DNA SEQ-NG blood targeted NGS with molecular inversion probes: coding exons of 27 genes associated with Joubert syndrome retinal disease 17 PubMed: Sun 2020 - F - China - - - - - 1 LOVD
+?/. - c.10601A>G r.(?) p.(Tyr3534Cys) - Unknown - likely pathogenic g.215955523T>C g.215782181T>C USH2A c.10601A>G, p.Tyr3534Cys - USH2A_002245 heterozygous PubMed: Thorsteinsson 2021 - - Unknown ? - - - - DNA SEQ-NG - retrospective analysis retinal disease US3 PubMed: Thorsteinsson 2021 - ? - Iceland - - - - - 1 LOVD
+?/. - c.10601A>G r.(?) p.(Tyr3534Cys) - Unknown - likely pathogenic g.215955523T>C g.215782181T>C USH2A c.10601A>G , p.Tyr3534Cys - USH2A_002245 heterozygous PubMed: Thorsteinsson 2021 - - Unknown ? - - - - DNA SEQ-NG - retrospective analysis retinal disease US4 PubMed: Thorsteinsson 2021 - ? - Iceland - - - - - 1 LOVD
?/. 54 c.10601A>G r.(?) p.(Tyr3534Cys) - Parent #2 ACMG VUS g.215955523T>C g.215782181T>C USH2A c.10601A>G, p.Tyr3534Cys - USH2A_002245 heterozygous PubMed: Meng 2020 - - Unknown ? - - - - DNA SEQ-NG-I blood hereditary eye disease enrichment panel (HEDEP) - 441 genes covering 14 Usher genes retinal disease 43 PubMed: Meng 2020 - F - China - - - - - 1 LOVD
?/. - c.10601A>G r.(?) p.(Tyr3534Cys) - Unknown ACMG VUS g.215955523T>C g.215782181T>C - - USH2A_002245 ACMG GN005 criteria: PM2_P PM3_P PubMed: Meng, X. et al., 2021; PubMed: Sun, Y. et al., 2020 - rs750231701 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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