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.

9 entries on 1 page. Showing entries 1 - 9.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

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DNA change (hg38)     

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ClinVar ID     

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Owner     
+/+ 5 c.820C>T r.(?) p.(Arg274*) Laminin N-terminal (271-517) Unknown - pathogenic g.216500961G>A g.216327619G>A - - USH2A_000289 Heterozygous; Pathogenic PubMed: Jaijo 2010 - - Germline - - -BcgI;-TaqI; - - DNA minigene, SEQ - - USH2 - PubMed: Jaijo 2010 Proband M - Spain - - - - - 1 Jose Maria Millan
+/+ 5 c.820C>T r.(?) p.(Arg274*) Laminin N-terminal (271-517) Parent #1 - pathogenic g.216500961G>A g.216327619G>A - - USH2A_000289 Heterozygous PubMed: Baux 2014 - - Germline - - -BcgI;-TaqI; - - DNA SEQ - - USH2 - PubMed: Baux 2014 Relative M - France - - - - - 1 Anne-Françoise Roux
+/+ 5 c.820C>T r.(?) p.(Arg274*) Laminin N-terminal (271-517) Paternal (confirmed) - pathogenic g.216500961G>A g.216327619G>A - - USH2A_000289 Heterozygous PubMed: Baux 2014 - - Germline - - -BcgI;-TaqI; - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband M - France - - - - - 1 Anne-Françoise Roux
+/+ 5 c.820C>T r.(?) p.(Arg274*) Laminin N-terminal (271-517) Parent #1 - pathogenic g.216500961G>A g.216327619G>A - - USH2A_000289 Heterozygous; Pathogenic PubMed: Garcia-Garcia 2011 - - Germline - - -BcgI;-TaqI; - - DNA SEQ - - USH2 - PubMed: Garcia-Garcia 2011 Proband M - Spain - - - - - 1 Jose Maria Millan
+/. - c.820C>T r.(?) p.(Arg274*) - Parent #1 - pathogenic g.216500961G>A g.216327619G>A - - USH2A_000289 4 heterozygous, no homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs397518036 Germline - 4/2795 individuals - - - DNA arraySNP - Infinium Global Screening Array v1.0 ? - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - 4 Mohammed Faruq
+?/. - c.820C>T r.(?) p.(Arg274*) - Unknown ACMG pathogenic g.216500961G>A - - - USH2A_000289 - - - - Germline/De novo (untested) - - - - - DNA SEQ-NG-I - - USH IR_GH_0031 - - M - Korea, South (Republic) - - - - - 1 Jinu Han
+/. - c.820C>T r.(?) p.(Arg274*) - Parent #1 ACMG pathogenic g.216500961G>A g.216327619G>A USH2A c.[820C>T];[15178T>C], V1: c.820C>T, (p.Arg274Ter) - USH2A_000289 alleles in trans; heterozygous PubMed: Chen 2021 - - Unknown ? - - - - DNA SEQ-NG blood 212 inherited retinal disease-related genes retinal disease F013 PubMed: Chen 2021 - ? - Taiwan - - - - - 1 LOVD
+/. - c.820C>T r.(?) p.(Arg274Ter) - Parent #1 - pathogenic g.216500961G>A g.216327619G>A USH2A c.[820C>T];[15178T>C]; p.(Arg274Ter) - USH2A_000289 heterozygous PubMed: Chen 2021 - - Germline yes Taiwan Biobank: 0; GnomAD_exome_East: 0; GnomAD_All: 0.00000797 - - - DNA SEQ-NG - targeted 212 IRD-related genes retinal disease F013 PubMed: Chen 2021 - - - Taiwan - - - - - 1 LOVD
+/. - c.820C>T r.(?) p.(Arg274Ter) - Unknown ACMG pathogenic g.216500961G>A g.216327619G>A - - USH2A_000289 ACMG GN005 criteria: PVS1_VS PM2_P PM3_S PubMed: Garcia-Garcia, G. et al., 2011 - rs397518036 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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