Variant #0001034800 (NC_000005.9:g.112824038_112824039insCGC, NM_152624.5:c.*474857_*474858insCGC (DCP2))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.112824038_112824039insCGC
DNA change (hg38) -
Published as MCC(NM_001085377.2):c.75_76insGGC (p.(Ser25_Ser26insGly))
ISCN -
DB-ID DCP2_000015
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     
MCC NM_001085377.1 -?/. - c.75_76insGGC r.(?) p.(Ser25_Ser26insGly)
TSSK1B NM_032028.3 -?/. - c.-53501_-53500insGGC r.(?) p.(=)
DCP2 NM_152624.5 -?/. - c.*474857_*474858insCGC r.(=) p.(=)


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