Variant #0000258241 (NC_000019.9:g.45409113C>T, NC_000019.9(NM_000041.2):c.-24+15C>T (APOE))
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.45409113C>T |
DNA change (hg38) |
g.44905856C>T |
Published as |
APOE(NM_000041.4):c.-24+15C>T, APOE(NM_001302688.2):c.-13C>T |
ISCN |
- |
DB-ID |
APOE_000003 See all 2 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) |
0.00139 View details |
Owner |
VKGL-NL_AMC |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_AMC |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2023-07-07 10:10:56 +02:00 (CEST) |

Variant on transcripts
|