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.

2 entries on 1 page. Showing entries 1 - 2.
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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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Tissue     

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Disease     

ID_report     

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VIP     

Data_av     

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Panel size     

Owner     
+/? 27i c.5573-834A>G r.(=) p.(=) - Unknown ACMG likely pathogenic g.216247476T>C g.216074134T>C - - USH2A_000949 Heterozygous; induces inclusion 131 and 73 bp (pseudo-exons) in minigenes; induces PE insertion Liquori et al., accepted - - Germline - 0/342 controls - - - DNA minigene, SEQ, SEQ-NG-S - - USH2 - Liquori accepted Proband M - France - - - - - 1 Anne-Françoise Roux
+?/. 27i c.5573-834A>G r.[=,5572_5573ins5573-969_5573-839,5572_5573ins5573-911_5573-839] p.? - Parent #2 ACMG likely pathogenic g.216247476T>C g.216074134T>C - - USH2A_000949 - PubMed: Reurink 2023, Journal: Reurink 2023 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease USH24 PubMed: Reurink 2023, Journal: Reurink 2023 - - - - - - - - - 1 Janine Reurink
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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