Variant #0000571321 (NC_000022.10:g.19511720C>A, NM_001178010.2:c.*3718C>A (CDC45))

Chromosome 22
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.19511720C>A
DNA change (hg38) g.19524197C>A
Published as CLDN5(NM_001130861.1):c.314G>T (p.(Gly105Val))
ISCN -
DB-ID CLDN5_000003
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) 2.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CDC45 NM_001178010.2 -?/. - c.*3718C>A r.(=) p.(=)
CLDN5 NM_003277.3 -?/. - c.314G>T r.(?) p.(Gly105Val)


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