Variant #0001042673 (NC_000019.9:g.14066816C>T, NM_138353.2:c.459C>T (DCAF15))

Chromosome 19
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.14066816C>T
DNA change (hg38) -
Published as DCAF15(NM_138353.3):c.459C>T (p.(Ile153=))
ISCN -
DB-ID DCAF15_000004
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) 0.00262 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 2025-05-05 21:14:00 +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     
PODNL1 NM_024825.3 -?/. - c.-17801G>A r.(?) p.(=)
DCAF15 NM_138353.2 -?/. - c.459C>T r.(?) p.(=)


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