Variant #0000867242 (NC_000023.10:g.1718162G>C, AKAP17A(NM_005088.2):c.989G>C)
Chromosome |
X |
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.1718162G>C |
DNA change (hg38) |
- |
Published as |
AKAP17A(NM_005088.2):c.989G>C (p.R330T) |
ISCN |
- |
DB-ID |
AKAP17A_000021 |
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) |
0.0002 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2022-05-09 16:01:56 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
|
|