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.

3 entries on 1 page. Showing entries 1 - 3.
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Effect     

Exon     

AscendingDNA change (cDNA)     

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DNA change (hg38)     

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+/+ 17 c.3722_3729delinsTCA r.(?) p.(Ala1241Valfs*8) - Parent #2 - pathogenic g.216373051_216373058delinsTGA g.216199709_216199716delinsTGA - - USH2A_000994 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband - - Slovenia - - - - - 1 Crystel Bonnet
+?/. - c.3722_3729delinsTCA r.(?) p.(Ala1241Valfs*8) - Parent #1 - likely pathogenic g.216373051_216373058delinsTGA g.216199709_216199716delinsTGA USH2A, variant 1: c.10073G>A/p.C3358Y, variant 2: c.3722_3729delinsTCA/ p.A1241Vfs*8 - USH2A_000994 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET9 targeted sequencing panel - see paper retinal disease 1264 PubMed: Weisschuh 2020 Filing key number: 1065, sporadic retinitis pigmentosa, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
+/. - c.3722_3729delinsTCA r.(?) p.(Ala1241ValfsTer8) - Unknown ACMG pathogenic g.216373051_216373058delinsTGA g.216199709_216199716delinsTGA - - USH2A_000994 ACMG GN005 criteria: PVS1_VS PM2_P PM3_M PubMed: Bonnet, C. et al., 2016; PubMed: Weisschuh, N. et al., 2020 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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