Variant #0000963365 (NC_000005.9:g.112824066_112824068dup, NM_152624.5:c.*474885_*474887dup (DCP2))

Chromosome 5
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.112824066_112824068dup
DNA change (hg38) -
Published as MCC(NM_001085377.2):c.61_63dupGGC (p.G21dup)
ISCN -
DB-ID DCP2_000012 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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-02-26 20:06:56 +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     
MCC NM_001085377.1 -/. - c.61_63dup r.(?) p.(Gly21dup)
TSSK1B NM_032028.3 -/. - c.-53515_-53513dup r.(?) p.(=)
DCP2 NM_152624.5 -/. - c.*474885_*474887dup r.(=) p.(=)


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