Full data view for gene PCDH15


This database is one of the ”Retinal and hearing impairment genetic variant databases”.
Information The variants shown are described using the 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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DB-ID     

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ClinVar ID     

dbSNP ID     

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VIP     

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ID_report     

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+/+ 28 c.3791_3794del r.(?) p.(Ile1264Lysfs*21) Unknown - pathogenic g.55616950_55616953del g.53857190_53857193del - - PCDH15_000162 heterozygous; likely pathogenic PubMed: Glöcke 2013 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Glöcke 2013 Proband - - - - - - - - 1 Anne-Françoise Roux
+?/. - c.3791_3794del r.(?) p.(Ile1264Lysfs*21) Parent #1 - likely pathogenic g.55616950_55616953del g.53857190_53857193del PCDH15, variant 1: c.3791_3794del/p.I1264fs*, variant 2 :Deletion exon 2 - PCDH15_000162 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET1 targeted sequencing panel - see paper retinal disease 70 PubMed: Weisschuh 2020 Filing key number: 35, Usher syndrome type I, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
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