Full data view for gene CERKL


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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ISCN     

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Variant remarks     

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ClinVar ID     

dbSNP ID     

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Re-site     

VIP     

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ID_report     

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Owner     
+?/. - c.1642T>G r.(?) p.(Tyr548Asp) Parent #1 - likely pathogenic g.182402946A>C g.181538219A>C CERKL, variant 1: c.481+2T>G/p.?, variant 2: c.1642T>G/p.Y548D - CERKL_000110 possibly solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET9 targeted sequencing panel - see paper retinal disease 1108 PubMed: Weisschuh 2020 Filing key number: 749, cone-rod dystrophy, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
+/. - c.1642T>G r.(?) p.(Tyr548Asp) Unknown ACMG pathogenic g.182402946A>C g.181538219A>C - - CERKL_000110 case unsolved PubMed: Hitti-Malin 2024, Journal: Hitti-Malin 2024 - - Germline - - - - - DNA SEQ - smMIP-based 105 iMD/AMD genes macular dystrophy 071781 PubMed: Hitti-Malin 2024, Journal: Hitti-Malin 2024 - - - - - - - - - 1 Johan den Dunnen
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