Variant #0000000094 (NC_000005.10:g.112780868C>G, NM_001127511.2:c.640C>G (APC))

Chromosome 5
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.112780868C>G
Published as -
Reference ClinVarN.A. Abdul Murad et al. (2012), dbSNP, ClinVar
DB-ID APC_000003
dbSNP ID rs188457893
Frequency 76
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MyHVP
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by MyHVP
Date created 2017-11-21 17:02:09 +08:00 (CST)
Date last edited 2021-09-08 14:27:56 +08:00 (CST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
APC NM_001127511.2 ?/. 5 c.640C>G - r.(?) p.(Leu214Val) - ClinVar