Variant #0000461218 (NC_000018.9:g.50450196T>C, NM_005215.3:c.817T>C (DCC))

Chromosome 18
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.50450196T>C
DNA change (hg38) g.52923826T>C
Published as -
ISCN -
DB-ID DCC_000032 See all 2 reported entries
Variant remarks CADD - 26.7, REVEL - 0.902, M-CAP - 0.624, MPC - 1.00
Reference PubMed: Bierhals 2018
ClinVar ID -
dbSNP ID -
Origin In silico
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Ashley Marsh
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2017-12-19 10:34:12 +01:00 (CET)
Date last edited 2020-07-14 19:07:53 +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 ?/. 4 c.817T>C r.(?) p.Trp273Arg -


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