Variant #0000001717 (NC_000017.10:-, AXIN2(NM_004655.3):c.1989G>A)
Chromosome |
17 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Type |
peripheral blood |
DNA change (genomic) (Relative to hg19 / GRCh37) |
- |
Reference |
GenBank |
DB-ID |
AXIN2_00001 |
Frequency |
- |
Variant remarks |
a novel c.1989G>A mutation which result in the lossing of the DIX domain will have functional consequences and destroy the inhibitory action of AXIN2 on WNT signaling. |
ClassClinical |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Qi Ming |
Database submission license |
No license selected |
Created by |
Qi Ming |

Variant on transcripts
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