Variant #0000244043 (NC_000001.10:g.11003171C>T, NM_007375.3:c.(642C>T) (TARDBP))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Effect unknown |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.11003171C>T |
| DNA change (hg38) |
g.10943114C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TARDBP_000148 |
| Variant remarks |
Silent point mutation in coding region |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Unknown |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Marc Cruts |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Julia Lopez |
| Date created |
2013-05-01 13:44:57 +02:00 (CEST) |
| Date last edited |
2018-11-09 14:00:33 +01:00 (CET) |

Variant on transcripts
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