Variant #0000000189 (NC_000005.9:g.112178781C>T, APC(NM_000038.5):c.7490C>T)

Chromosome 5
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.112178781C>T
Reference -
DB-ID APC_000001
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00036 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
APC NM_000038.5 ?/? - c.7490C>T r.(?) p.(Ser2497Leu)