Full data view for gene KCNV2

This database is one of the ""Eye disease"" gene variant databases.""
Information The variants shown are described using the NM_133497.3 transcript reference sequence.

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Allele     

Classification method     

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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Re-site     

VIP     

Methylation     

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Tissue     

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Disease     

ID_report     

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Owner     
+?/. - c.1186G>T r.(?) p.(Gly396*) Parent #1 - likely pathogenic g.2718925G>T g.2718925G>T KCNV2, variant 1: c.1186G>T/p.G396* , variant 2 :Deletion exon 1 - KCNV2_000153 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET9 targeted sequencing panel - see paper retinal disease 1034 PubMed: Weisschuh 2020 Filing key number: 599, cone dystrophy, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
?/. - c.1186G>T r.(?) p.(Gly396*) Parent #1 - VUS g.2718925G>T g.2718925G>T KCNV2 c.1186G>T, p.(Gly396*) - KCNV2_000153 heterozygous PubMed: Georgiou 2021 - - Unknown ? - - - - DNA SEQ-NG, SEQ blood multiple centers, various techniques retinal disease ZD 599_ZD599-29894 PubMed: Georgiou 2021 family ZD 599, individual ZD599-29894 F - Germany - - - - - 1 LOVD
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