Variant #0001039744 (NC_000013.10:g.77900871_77900873dup, NM_015057.4:c.42_44dup (MYCBP2))

Chromosome 13
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.77900871_77900873dup
DNA change (hg38) -
Published as MYCBP2(NM_015057.5):c.42_44dup (p.(Ser15dup))
ISCN -
DB-ID MYCBP2_000041
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 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     
MYCBP2 NM_015057.4 ?/. - c.42_44dup r.(?) p.(Ser15dup)


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