Full data view for gene USH1G


This database is one of the ”Retinal and hearing impairment genetic variant databases”.
Information The variants shown are described using the NM_173477.2 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

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DNA change (genomic) (hg19)     

DNA change (hg38)     

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Owner     
+?/. - c.208_209insTC r.(?) p.(His70Leufs*26) - Parent #1 - likely pathogenic g.72916723_72916724insAG g.74920628_74920629insAG USH1G, variant 1: c.208_209insTC/p.H70Lfs*26, variant 2: c.208_209insTC/p.H70Lfs*26 - USH1G_000072 solved, homozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET9 targeted sequencing panel - see paper retinal disease 208 PubMed: Weisschuh 2020 Filing key number: 74, Usher syndrome type I, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
+?/. - c.208_209insTC r.(?) p.(His70Leufs*26) - Parent #1 - likely pathogenic g.72916723_72916724insAG g.74920628_74920629insAG USH1G, variant 1: c.208_209insTC/p.H70Lfs*26, variant 2: c.208_209insTC/p.H70Lfs*26 - USH1G_000072 solved, homozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ blood Sanger sequencing retinal disease 209 PubMed: Weisschuh 2020 Filing key number: 74, Usher syndrome type I, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
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