Variant #0000894206 (NC_000017.10:g.63534353T>C, NM_004655.3:c.1168A>G (AXIN2))
Chromosome |
17 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.63534353T>C |
DNA change (hg38) |
- |
Published as |
AXIN2(NM_004655.3):c.1168A>G (p.S390G, p.(Ser390Gly)), AXIN2(NM_004655.4):c.1168A>G (p.S390G) |
ISCN |
- |
DB-ID |
AXIN2_000010 See all 7 reported entries |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00077 View details |
Owner |
VKGL-NL_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2022-11-01 13:41:49 +01:00 (CET) |
Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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