Variant #0000461220 (NC_000018.9:g.50683873G>A, NM_005215.3:c.1409G>A (DCC))

Chromosome 18
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.50683873G>A
DNA change (hg38) g.53157503G>A
Published as -
ISCN -
DB-ID DCC_000015 See all 4 reported entries
Variant remarks significantly decreased EGR1-promoter activation, impaired cytoskeletal and membrane rearrangement, CADD = D, GERP = 5.4
Reference -
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00284 View details
Owner Ashley Marsh
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2018-04-12 04:39:09 +02:00 (CEST)
Date last edited 2020-07-14 19:08:02 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
DCC NM_005215.3 +/. - c.1409G>A r.(?) p.Gly470Asp -


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