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.

7 entries on 1 page. Showing entries 1 - 7.
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Effect     

Exon     

AscendingDNA change (cDNA)     

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+/+ 63 c.13257_13263del r.(?) p.(Phe4419Leufs*2) Fibronectin type-III 29 (4356-4439) Unknown - pathogenic g.215847993_215847999del g.215674651_215674657del - - USH2A_000759 Heterozygous; likely pathogenic PubMed: Glöckle 2014 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - RPar - PubMed: Glöckle 2014 Proband - - - - - - - - 1 Anne-Françoise Roux
+/+ 63 c.13257_13263del r.(?) p.(Phe4419Leufs*2) Fibronectin type-III 29 (4356-4439) Unknown - pathogenic g.215847993_215847999del g.215674651_215674657del - - USH2A_000759 Heterozygous; causative PubMed: Eisenberger 2013 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - RPar - PubMed: Eisenberger 2013 Proband M - Germany - - - - - 1 Anne-Françoise Roux
+/. 63 c.13257_13263del r.(?) p.(Phe4419Leufs*2) - Unknown - pathogenic g.215847990_215847996del - c.13257_13263del - USH2A_000759 - PubMed: Eisenberger-2013 - - Germline - - - - - DNA SEQ-NG-I, SEQ-NG-R, SEQ blood - retinal disease - PubMed: Eisenberger-2013 - M no Germany - - - - - 1 LOVD
+?/. - c.13257_13263del r.(?) p.(Phe4419Leufs*2) - Parent #1 - likely pathogenic g.215847993_215847999del g.215674651_215674657del USH2A, variant 1: c.2276G>T/p.C759F, variant 2: c.13257_13263del/ p.F4419Lfs*2 - USH2A_000759 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET3 targeted sequencing panel - see paper retinal disease 495 PubMed: Weisschuh 2020 Filing key number: 163, autosomal recessive retinitis pigmentosa, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
+?/. - c.13257_13263del r.(?) p.(Phe4419Leufs*2) - Parent #1 - likely pathogenic g.215847993_215847999del g.215674651_215674657del USH2A, variant 1: c.2276G>T/p.C759F, variant 2: c.13257_13263del/ p.F4419Lfs*2 - USH2A_000759 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ blood Sanger sequencing retinal disease 496 PubMed: Weisschuh 2020 Filing key number: 163, autosomal recessive retinitis pigmentosa, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
+/. - c.13257_13263del r.(?) p.(Phe4419Leufs*2) - Parent #1 - pathogenic g.215847993_215847999del g.215674651_215674657del USH2A c.13257_13263del, p.(Phe4419Leufs1*) - USH2A_000759 error in annotation, frameshift causes stop after 2 amino acids, not 1, should be: p.(Phe4419Leufs*2); heterozygous PubMed: Falsini 2021 - - Germline yes - - - - DNA SEQ-NG-I - retrospective study (warning: duplicates in database possible) retinal disease 14 PubMed: Falsini 2021 - M - Italy - - - - - 1 LOVD
+/. - c.13257_13263del r.(?) p.(Phe4419LeufsTer2) - Unknown ACMG pathogenic g.215847993_215847999del g.215674651_215674657del - - USH2A_000759 ACMG GN005 criteria: PVS1_VS PM2_P PM3_M PP1_P PubMed: Falsini, B. et al., 2021; PubMed: Glockle, N. et al., 2014; PubMed: Weisschuh, N. et al., 2020 - rs1057517533 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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