Variant #0000994561 (NC_000005.9:g.112389537A>C, NM_152624.5:c.*40356A>C (DCP2))

Chromosome 5
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.112389537A>C
DNA change (hg38) -
Published as MCC(NM_001085377.1):c.2333T>G (p.(Leu778Arg))
ISCN -
DB-ID DCP2_000014
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 2024-08-28 13:16:32 +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.2333T>G r.(?) p.(Leu778Arg)
TSSK1B NM_032028.3 ?/. - c.*379896T>G r.(=) p.(=)
DCP2 NM_152624.5 ?/. - c.*40356A>C r.(=) p.(=)


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