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.

5 entries on 1 page. Showing entries 1 - 5.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

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DNA change (hg38)     

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DB-ID     

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Reference     

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+/+ 28 c.5614_5620del r.(?) p.(Ala1872Leufs*58) Fibronectin type-III 5 (1871-1949) Unknown - pathogenic g.216246595_216246601del g.216073253_216073259del 5614_5620delGCTGTCG - USH2A_000597 Heterozygous; Pathogenic PubMed: Le Quesne Stabej 2012 - - Germline - - -HincII;-Hpy166II;-DraIII;-HpaI; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/+ 28 c.5614_5620del r.(?) p.(Ala1872Leufs*58) Fibronectin type-III 5 (1871-1949) Unknown - pathogenic g.216246595_216246601del g.216073253_216073259del 5614_5620delGCTGTCG - USH2A_000597 Heterozygous; Pathogenic PubMed: Le Quesne Stabej 2012 - - Germline - - -HincII;-Hpy166II;-DraIII;-HpaI; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+?/. 28 c.5614_5620del r.(?) p.(Ala1872Leufs*58) - Unknown - likely pathogenic g.216246595_216246601del - c.5614_5620del - USH2A_000597 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
+?/. - c.5614_5620del r.(?) p.(Ala1872Leufs*58) - Parent #2 - likely pathogenic g.216246595_216246601del g.216073253_216073259del USH2A c.5614_5620del - USH2A_000597 protein variant annotation not written; heterozygous PubMed: Toms 2020 - - Unknown ? - - - - ? ? - retrospective cohort retinal disease 46 PubMed: Toms 2020 - ? - United Kingdom (Great Britain) - - - - - 1 LOVD
+/. - c.5614_5620del r.(?) p.(Ala1872LeufsTer58) - Unknown ACMG pathogenic g.216246595_216246601del g.216073253_216073259del - - USH2A_000597 ACMG GN005 criteria: PVS1_VS PM2_P PM3_M PubMed: Le Quesne Stabej, P. et al., 2012 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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