Variant #0001040510 (NC_000015.9:g.65935315C>T, NC_000015.9(NM_004727.2):c.2054-1450C>T (SLC24A1))

Chromosome 15
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.65935315C>T
DNA change (hg38) -
Published as SLC24A1(NM_001254740.2):c.5C>T (p.(Pro2Leu))
ISCN -
DB-ID DENND4A_000039
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) 3.0E-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 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     
SLC24A1 NM_004727.2 -?/. - c.2054-1450C>T r.(=) p.(=)
DENND4A NM_005848.3 -?/. - c.*18874G>A r.(=) p.(=)


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