Variant #0001005894 (NC_000022.10:g.19506390C>T, NM_001178010.2:c.1756C>T (CDC45))

Chromosome 22
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.19506390C>T
DNA change (hg38) -
Published as CDC45(NM_001178010.2):c.1756C>T (p.R586W)
ISCN -
DB-ID CLDN5_000005
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 6.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CDC45 NM_001178010.2 +/. - c.1756C>T r.(?) p.(Arg586Trp)
CLDN5 NM_003277.3 +/. - c.*4732G>A r.(=) p.(=)


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