Variant #0000000095 (NC_000005.10:g.112841553A>G, NM_000038.5:c.5959A>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.112841553A>G
Published as -
Reference N.A. Abdul Murad et al. (2012), dbSNP
DB-ID APC_000004
dbSNP ID rs1269798265
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 17:05:04 +08:00 (CST)
Date last edited 2021-09-08 14:58:33 +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.5959A>G - r.(?) p.(Ile1987Val) - ClinVar