Variant #0000567362 (NC_000019.9:g.40741862C>A, NM_001626.4:c.1110G>T (AKT2))
Chromosome |
19 |
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.40741862C>A |
DNA change (hg38) |
g.40235955C>A |
Published as |
AKT2(NM_001243027.1):c.924G>T (p.(Pro308=)), AKT2(NM_001626.5):c.1110G>T (p.P370=), AKT2(NM_001626.6):c.1110G>T (p.P370=) |
ISCN |
- |
DB-ID |
AKT2_000004 See all 3 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) |
0.0036 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2022-11-01 13:01:21 +01:00 (CET) |

Variant on transcripts
|