Variant #0000276163 (NC_000006.11:g.132058576_132058579del, NM_001145659.1:c.-26417_-26414del (CTAGE9))
| Chromosome |
6 |
| 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.132058576_132058579del |
| DNA change (hg38) |
g.131737436_131737439del |
| Published as |
ENPP3(NM_005021.4):c.2166_2167+2delAAGT |
| ISCN |
- |
| DB-ID |
ENPP3_000005 |
| 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 |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2020-06-22 10:23:50 +02:00 (CEST) |

Variant on transcripts
|