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.

4 entries on 1 page. Showing entries 1 - 4.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

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Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

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Re-site     

VIP     

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Disease     

ID_report     

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Owner     
+?/. - c.4385C>T r.(?) p.(Thr1462Ile) - Both (homozygous) - likely pathogenic (recessive) g.216363576G>A g.216190234G>A - - USH2A_001771 - PubMed: Fuster-Garcia 2018 - - Germline - - - - - DNA arraySEQ - - retinal disease RP1869 PubMed: Fuster-Garcia 2018 analysis 77 USH patients - - Spain - - - - - 1 Global Variome, with Curator vacancy
+?/. - c.4385C>T r.(?) p.(Thr1462Ile) - Paternal (confirmed) ACMG likely pathogenic g.216363576G>A - - - USH2A_001771 - PubMed: Mansard et al, 2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - USH2A - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
?/. 20 c.4385C>T r.(?) p.(Thr1462Ile) - Parent #1 - VUS g.216363576G>A - c.4385C>T - USH2A_001771 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - M - - - - - - - 1 Daan Panneman
?/. - c.4385C>T r.(?) p.(Thr1462Ile) - Unknown ACMG VUS g.216363576G>A g.216190234G>A - - USH2A_001771 ACMG GN005 criteria: PM2_P PM3_M PubMed: Mansard, L. et al., 2021 - rs2034687815 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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