Variant #0000565233 (NC_000018.9:g.60052034A>G, NM_003839.3:c.1618A>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.60052034A>G |
DNA change (hg38) |
g.62384801A>G |
Published as |
TNFRSF11A(NM_001278268.1):c.1576A>G (p.M526V), TNFRSF11A(NM_003839.2):c.1618A>G (p.M540V), TNFRSF11A(NM_003839.4):c.1618A>G (p.M540V) |
ISCN |
- |
DB-ID |
TNFRSF11A_000016 See all 4 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) |
0.00068 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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