Variant #0000001764 (NC_000017.10:-, AXIN2(NM_004655.3):c.143C>T)

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type peripheral columnar cells
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID AXIN2_00045
Frequency -
Variant remarks Other Wnt signaling members or alternative pathways

involved in the degradation of b-catenin should be subject

of further investigation.
ClassClinical -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AXIN2 NM_004655.3 ./. 02 c.143C>T - p.Pro48Leu