Variant #0000567783 (NC_000019.9:g.46283189dup, NC_000019.9(NM_004409.3):c.161-58dup (DMPK))
| Chromosome |
19 |
| 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.46283189dup |
| DNA change (hg38) |
g.45779931dup |
| Published as |
DMPK(NM_001081563.1):c.133dupC (p.(Leu45ProfsTer9)), DMPK(NM_001081563.2):c.133dupC (p.L45Pfs*9) |
| ISCN |
- |
| DB-ID |
DMPK_000035 See all 2 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) |
Retrieve |
| 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 |
2019-12-04 15:24:38 +01:00 (CET) |

Variant on transcripts
|