Variant #0001090029 (NC_000002.11:g.16085625_16085633dup, NM_005378.4:c.801_809dup (MYCN))

Chromosome 2
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.16085625_16085633dup
DNA change (hg38) -
Published as -
ISCN -
DB-ID chr2_024670
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-09-29 15:50:02 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYCN NM_005378.4 ?/. - c.801_809dup r.(?) p.(Asp267_Glu269dup)


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