Variant #0000689391 (NC_000005.9:g.112384920G>A, NM_152624.5:c.*35739G>A (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.112384920G>A
DNA change (hg38) -
Published as MCC(NM_001085377.1):c.2525C>T (p.T842M)
ISCN -
DB-ID DCP2_000013
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) 9.0E-5 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 2020-09-15 15:50:26 +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.2525C>T r.(?) p.(Thr842Met)
TSSK1B NM_032028.3 ?/. - c.*384513C>T r.(=) p.(=)
DCP2 NM_152624.5 ?/. - c.*35739G>A r.(=) p.(=)


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