Variant #0000525169 (NC_000005.9:g.170837540_170837541insTCTG, NM_002520.6:c.856_857insTCTG (NPM1))
| Chromosome |
5 |
| 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.170837540_170837541insTCTG |
| DNA change (hg38) |
g.171410536_171410537insTCTG |
| Published as |
NPM1(NM_002520.6):c.856_857insTCTG (p.D286Vfs*2) |
| ISCN |
- |
| DB-ID |
NPM1_000006 |
| 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_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2020-06-18 09:20:54 +02:00 (CEST) |

Variant on transcripts
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