Variant #0000658408 (NC_000018.9:g.50432528A>G, NM_005215.3:c.527A>G (DCC))

Chromosome 18
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.50432528A>G
DNA change (hg38) g.52906158A>G
Published as DCC(NM_005215.3):c.527A>G (p.N176S), DCC(NM_005215.4):c.527A>G (p.(Asn176Ser), p.N176S)
ISCN -
DB-ID DCC_000008 See all 6 reported entries
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) 0.00013 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 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +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.527A>G r.(?) p.(Asn176Ser) -


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