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     

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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.497A>G r.(?) p.(Glu166Gly) - Unknown ACMG likely pathogenic g.216592010T>C g.216418668T>C - - USH2A_001712 - PubMed: Karali 2019, Journal: Karali 2019 - - Germline - - - - - DNA SEQ-NG - clinical exome sequencing retinal disease Fam8P10 PubMed: Karali 2019, Journal: Karali 2019 family, 2 affected - - Italy - - - - - 2 Sandro Banfi
+/. - c.497A>G r.(?) p.(Glu166Gly) - Parent #1 - pathogenic (recessive) g.216592010T>C g.216418668T>C - - USH2A_001712 - PubMed: Karali 2019, Journal: Karali 2019 - - Germline - - - - - DNA SEQ-NG - - retinal disease Fam8P11 PubMed: Karali 2019, Journal: Karali 2019 - - - Italy - - - - - 1 Sandro Banfi
+?/. 3 c.497A>G r.(?) p.(Glu166Gly) - Unknown - likely pathogenic g.216592010T>C g.216418668T>C USH2A Ex.3 c.497A>G p.(Glu166Gly), IVS12 c.2168-1G>C p.(?), ABCA4: Ex.45 c.6148G>A p.(Val2050Leu) - USH2A_001712 compound heterozygous PubMed: Martin Merida 2019 - - Germline/De novo (untested) ? - - - - DNA SEQ-NG-I - - retinal disease RP-1370 PubMed: Martin Merida 2019 - ? - Spain - - - - - 1 LOVD
?/. - c.497A>G r.(?) p.(Glu166Gly) - Unknown ACMG VUS g.216592010T>C g.216418668T>C - - USH2A_001712 ACMG GN005 criteria: PM2_P PM3_P PubMed: Karali, M. et al., 2019 - rs747778052 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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