Variant #0000523856 (NC_000005.9:g.112676297C>T, NM_152624.5:c.*327116C>T (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.112676297C>T
DNA change (hg38) g.113340600C>T
Published as MCC(NM_001085377.1):c.546G>A (p.Q182=)
ISCN -
DB-ID DCP2_000008
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) 0.00738 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MCC NM_001085377.1 -/. - c.546G>A r.(?) p.(Gln182=)
TSSK1B NM_032028.3 -/. - c.*93136G>A r.(=) p.(=)
DCP2 NM_152624.5 -/. - c.*327116C>T r.(=) p.(=)


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