Variant #0000560433 (NC_000017.10:g.16852187A>G, NM_012452.2:c.310T>C (TNFRSF13B))
Chromosome |
17 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.16852187A>G |
DNA change (hg38) |
g.16948873A>G |
Published as |
TNFRSF13B(NM_012452.2):c.310T>C (p.C104R), TNFRSF13B(NM_012452.3):c.310T>C (p.(Cys104Arg), p.C104R) |
ISCN |
- |
DB-ID |
TNFRSF13B_000010 See all 7 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) |
0.00349 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 |
2025-05-05 21:14:00 +02:00 (CEST) |

Variant on transcripts
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