Variant #0000865745 (NC_000018.9:g.60052182C>G, NM_003839.3:c.1766C>G (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.60052182C>G |
DNA change (hg38) |
- |
Published as |
TNFRSF11A(NM_001278268.1):c.1724C>G (p.P575R) |
ISCN |
- |
DB-ID |
TNFRSF11A_000044 |
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) |
0.00013 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
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