Variant #0000311911 (NC_000008.10:g.22926313G>A, NM_003842.4:c.95C>T (TNFRSF10B))
Chromosome |
8 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.22926313G>A |
DNA change (hg38) |
g.23068800G>A |
Published as |
LOC286059(NR_038873.1):n.192+380G>A, TNFRSF10B(NM_003842.5):c.95C>T (p.P32L) |
ISCN |
- |
DB-ID |
TNFRSF10B_000003 See all 5 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) |
0.67935 View details |
Owner |
VKGL-NL_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2021-09-17 14:40:49 +02:00 (CEST) |

Variant on transcripts
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