Variant #0001013921 (NC_000004.11:g.103517449G>A, NM_001165412.1:c.1452G>A (NFKB1))
Chromosome |
4 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.103517449G>A |
DNA change (hg38) |
- |
Published as |
NFKB1(NM_003998.4):c.1455G>A (p.T485=) |
ISCN |
- |
DB-ID |
NFKB1_000048 |
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) |
4.0E-5 View details |
Owner |
VKGL-NL_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2024-10-29 21:08:56 +01:00 (CET) |
Date last edited |
2025-02-07 18:57:27 +01:00 (CET) |

Variant on transcripts
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