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     

Classification method     

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     
+?/? 44 c.8755A>C r.(=) p.(Thr2919Pro) Fibronectin type-III 15 (2821-2920) Unknown ACMG VUS g.216040439T>G g.215867097T>G - - USH2A_000835 Heterozygous; mutation PubMed: Krawitz 2014, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ-NG-S - - USH2 - PubMed: Krawitz 2014 Proband M - Germany - - - - - 1 Peter Krawitz
+?/? 44 c.8755A>C r.(?) p.(Thr2919Pro) Fibronectin type-III 15 (2821-2920) Parent #2 ACMG VUS g.216040439T>G g.215867097T>G - - USH2A_000835 Heterozygous; mutation PubMed: Bonnet 2016, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband M - Germany - - - - - 1 Crystel Bonnet
?/. - c.8755A>C r.(?) p.(Thr2919Pro) - Unknown ACMG VUS g.216040439T>G g.215867097T>G - - USH2A_000835 ACMG GN005 criteria: PM2_P PM3_P PubMed: Bonnet, C. et al., 2016 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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