Variant #0001024885 (NC_000004.11:g.119674060_119674061dup, NC_000004.11(NM_014822.2):c.1422-10_1422-9dup (SEC24D))

Chromosome 4
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.119674060_119674061dup
DNA change (hg38) -
Published as SEC24D(NM_001318066.2):c.1425-10_1425-9dupTT
ISCN -
DB-ID SEC24D_000058
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2025-02-07 18:57:27 +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     
SEC24D NM_014822.2 -/. - c.1422-10_1422-9dup r.(=) p.(=)


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