Variant #0001055166 (NC_000015.9:g.65917172_65917173del, NM_004727.2:c.754_755del (SLC24A1))

Chromosome 15
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.65917172_65917173del
DNA change (hg38) -
Published as SLC24A1(NM_004727.3):c.754_755del (p.(Met252ValfsTer2))
ISCN -
DB-ID SLC24A1_000031 See all 4 reported entries
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) 0.0001 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 2025-11-01 13:22:20 +01:00 (CET)
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.754_755del r.(?) p.(Met252Valfs*2)
DENND4A NM_005848.3 +/. - c.*37016_*37017del r.(=) p.(=)


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