Variant #0001039792 (NC_000014.8:g.104027410C>G, NM_032374.3:c.-1890C>G (APOPT1))
| Chromosome |
14 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.104027410C>G |
| DNA change (hg38) |
- |
| Published as |
BAG5(NM_001015048.3):c.92G>C (p.(Ser31Thr)), BAG5(NM_001015049.3):c.215G>C (p.S72T) |
| ISCN |
- |
| DB-ID |
APOPT1_000013 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) |
0.00156 View details |
| Owner |
VKGL-NL_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2025-05-05 21:14:00 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
|