Variant #0000808562 (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) |
- |
| 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_Groningen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Groningen |
| Date created |
2021-09-17 14:40:49 +02:00 (CEST) |
| Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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