Variant #0000609399 (NC_000005.9:g.112399697A>T, NM_152624.5:c.*50516A>T (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.112399697A>T
DNA change (hg38) g.113064000A>T
Published as MCC(NM_001085377.1):c.2197T>A (p.S733T)
ISCN -
DB-ID DCP2_000010
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_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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MCC NM_001085377.1 ?/. - c.2197T>A r.(?) p.(Ser733Thr)
TSSK1B NM_032028.3 ?/. - c.*369736T>A r.(=) p.(=)
DCP2 NM_152624.5 ?/. - c.*50516A>T r.(=) p.(=)


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