Full data view for gene CEP78

This database is one of the "Eye disease" gene variant databases.
Information The variants shown are described using the NM_001098802.1 transcript reference sequence.

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

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Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

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Disease     

ID_report     

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Owner     
+?/. - c.1427del r.(?) p.(Val476Glyfs*2) Parent #1 - likely pathogenic g.80877866del g.78262950del CEP78, variant 1: c.1403_1405delinsCTTT/ p.L468Pfs*13 , variant 2: c.1427del/p.V476Gfs*2 - CEP78_000042 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET9 targeted sequencing panel - see paper retinal disease 542 PubMed: Weisschuh 2020 Filing key number: 191, cone-rod dystrophy, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
+/. - c.1427del r.(?) p.(Val476GlyfsTer2) Both (homozygous) ACMG pathogenic (recessive) g.80877866del g.78262950del - - CEP78_000042 ACMG PM2, PVS1, PP5 PubMed: Weisschuh 2024 813161 - Germline - - - - - DNA SEQ-NG - WGS ? CRD-812 PubMed: Weisschuh 2024 patient, no family history F - Germany - - - - - 1 Johan den Dunnen
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