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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VIP     

Data_av     

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Owner     
+/+ 43 c.8603del r.(?) p.(Asn2868Ilefs*6) Fibronectin type-III 15 (2821-2920) Parent #2 - pathogenic g.216051180del g.215877838del 8602delA - USH2A_000787 Heterozygous; Mutation PubMed: Huang 2013 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Huang 2013 Proband F - China - - - - - 1 Anne-Françoise Roux
+?/. - c.8603del r.(?) p.(Asn2868IlefsTer6) - Parent #2 - likely pathogenic g.216051180del g.215877838del 8603delA - USH2A_000787 - - - - Germline yes - - - - DNA SEQ-NG - 284 gene panel retinal disease W56-1 PubMed: Huang 2015 - M - China - - - - - 1 LOVD
+/. 43 c.8603del r.(?) p.(Asn2868Ilefs*6) - Parent #2 ACMG pathogenic g.216051180del g.215877838del USH2A c.8603delA, p.(Asn2868Ilefs*6) - USH2A_000787 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease W56-1 PubMed: Zhu 2021 family 240, patient W56-1 M - China - - - - - 1 LOVD
+/. - c.8603del r.(?) p.(Asn2868IlefsTer6) - Unknown ACMG pathogenic g.216051180del g.215877838del 8603delA - USH2A_000787 ACMG GN005 criteria: PVS1_VS PM2_P PM3_P PubMed: Huang, X. F. et al., 2013 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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