Variant #0000946933 (NC_000001.10:g.114439059C>A, NM_006594.3:c.1331G>T (AP4B1))
Chromosome |
1 |
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.114439059C>A |
DNA change (hg38) |
- |
Published as |
AP4B1(NM_006594.5):c.1331G>T (p.G444V) |
ISCN |
- |
DB-ID |
AP4B1_000021 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) |
Retrieve |
Owner |
VKGL-NL_VUmc |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_VUmc |
Date created |
2023-11-27 17:35:39 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
|