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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ISCN     

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Owner     
+/+ 1 c.84dup r.(?) p.(Asp29Argfs*29) - Both (homozygous) - pathogenic g.72919089dup g.74922994dup - - USH1G_000011 homozygous PubMed: Bonnet et al., 2011 - - Germline - - none - - DNA SEQ - - USH1 - PubMed: Bonnet et al., 2011 proband - - - - - - - - 1 Anne-Françoise Roux
+?/. - c.84dup r.(?) p.(Asp29Argfs*29) - Parent #1 - likely pathogenic g.72919089dup g.74922994dup USH1G, variant 1: c.84dup/p.D29Rfs*29, variant 2: c.84dup/p.D29Rfs*29 - USH1G_000011 solved, homozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET3 targeted sequencing panel - see paper retinal disease 21 PubMed: Weisschuh 2020 Filing key number: 11, Usher syndrome type I, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
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