Variant #0000341229 (NC_000017.10:g.16843729G>T, NM_012452.2:c.542C>A (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.16843729G>T |
| DNA change (hg38) |
g.16940415G>T |
| Published as |
TNFRSF13B(NM_012452.2):c.542C>A (p.A181E), TNFRSF13B(NM_012452.3):c.542C>A (p.(Ala181Glu), p.A181E) |
| ISCN |
- |
| DB-ID |
TNFRSF13B_000009 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) |
0.00544 View details |
| Owner |
VKGL-NL_Nijmegen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Nijmegen |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2024-08-28 13:16:32 +02:00 (CEST) |

Variant on transcripts
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