Variant #0001066252 (NC_000015.9:g.65943119_65943130dup, NM_004727.2:c.2632_2643dup (SLC24A1))

Chromosome 15
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.65943119_65943130dup
DNA change (hg38) -
Published as SLC24A1(NM_004727.2):c.2632_2643dupCAGGAGGAAGAG (p.Q878_E881dup), SLC24A1(NM_004727.3):c.2632_2643dup (p.(Gln878_Glu881dup))
ISCN -
DB-ID DENND4A_000014 See all 2 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2026-01-20 18:57:21 +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.2632_2643dup r.(?) p.(Gln878_Glu881dup)
DENND4A NM_005848.3 ?/. - c.*11070_*11081dup r.(=) p.(=)


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