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.

3 entries on 1 page. Showing entries 1 - 3.
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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     

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Panel size     

Owner     
+/+ 48 c.9492_9498del r.(?) p.(Asp3165Serfs*5) Fibronectin type-III 18 (3110-3200) Paternal (inferred) - pathogenic g.215990414_215990420del g.215817072_215817078del - - USH2A_000746 Heterozygous; Disease causing PubMed: Xu 2011 - - Germline - 0/200 controls none - - DNA PCRdig, SEQ - - USH2 - PubMed: Xu 2011 Proband M - China - - - - - 1 Anne-Françoise Roux
+/. - c.9492_9498del r.(?) p.(Asp3165Serfs*5) - Parent #2 ACMG pathogenic (recessive) g.215990414_215990420del g.215817072_215817078del c.9492_9498delTGATGAG - USH2A_000746 - PubMed: Sun 2018 - - Germline - - - - - DNA SEQ - - HL 19082 PubMed: Sun 2018 sporadic case - no China - - - - - 1 LOVD
+/. - c.9492_9498del r.(?) p.(Asp3165SerfsTer5) - Unknown ACMG pathogenic g.215990414_215990420del g.215817072_215817078del - - USH2A_000746 ACMG GN005 criteria: PVS1_VS PM2_P PM3_M PubMed: Sun, T. et al., 2018 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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