Variant #0000000093 (NC_000005.10:g.112841589C>G, NM_000038.5:c.5995C>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.112841589C>G
Published as -
Reference N.A. Abdul Murad et al. (2012), dbSNP, ClinVar
DB-ID APC_000002
dbSNP ID rs1554087136
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 16:58:03 +08:00 (CST)
Date last edited 2021-09-08 15:03:37 +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_000038.5 ?/. 11i_15i c.5995C>G - r.(?) p.(Pro1999Ala) - ClinVar