Variant #0000609400 (NC_000005.9:g.112439988G>A, NM_152624.5:c.*90807G>A (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.112439988G>A
DNA change (hg38) g.113104291G>A
Published as MCC(NM_001085377.1):c.1092C>T (p.C364=)
ISCN -
DB-ID DCP2_000011
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 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-06-17 14:37:35 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MCC NM_001085377.1 -?/. - c.1092C>T r.(?) p.(Cys364=)
TSSK1B NM_032028.3 -?/. - c.*329445C>T r.(=) p.(=)
DCP2 NM_152624.5 -?/. - c.*90807G>A r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.