Variant #0000808559 (NC_000018.9:g.60015434G>A, NM_003839.3:c.109G>A (TNFRSF11A))
| Chromosome |
18 |
| 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.60015434G>A |
| DNA change (hg38) |
- |
| Published as |
TNFRSF11A(NM_001270949.1):c.109G>A (p.(Glu37Lys)), TNFRSF11A(NM_001278268.1):c.109G>A (p.E37K), TNFRSF11A(NM_003839.2):c.109G>A (p.E37K) |
| ISCN |
- |
| DB-ID |
TNFRSF11A_000037 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) |
3.0E-5 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2021-09-17 14:40:49 +02:00 (CEST) |
| Date last edited |
2023-04-16 21:50:28 +02:00 (CEST) |

Variant on transcripts
|