Variant #0000617679 (NC_000019.9:g.45411793G>A, NM_000041.2:c.240G>A (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.45411793G>A |
DNA change (hg38) |
g.44908536G>A |
Published as |
APOE(NM_001302688.2):c.318G>A (p.A106=) |
ISCN |
- |
DB-ID |
APOE_000062 |
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) |
2.0E-5 View details |
Owner |
VKGL-NL_AMC |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_AMC |
Date created |
2019-12-04 15:24:38 +01:00 (CET) |
Date last edited |
2020-07-16 09:23:33 +02:00 (CEST) |

Variant on transcripts
|