Variant #0000855350 (NC_000018.9:g.60015434G>A, NM_003839.3:c.109G>A (TNFRSF11A))
Chromosome |
18 |
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.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_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2022-05-09 15:47:41 +02:00 (CEST) |
Date last edited |
2023-04-16 21:50:28 +02:00 (CEST) |

Variant on transcripts
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