Variant #0000304394 (NC_000006.11:g.32191688_32191690del, NM_004557.3:c.45_47del (NOTCH4))
| Chromosome |
6 |
| 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.32191688_32191690del |
| DNA change (hg38) |
g.32223911_32223913del |
| Published as |
NOTCH4(NM_004557.3):c.33_35del (p.(Leu16del)), NOTCH4(NM_004557.3):c.45_47delGCT (p.L16del), NOTCH4(NM_004557.4):c.45_47delGCT (p.L16del) |
| ISCN |
- |
| DB-ID |
NOTCH4_000011 See all 3 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 |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2024-04-19 20:27:30 +02:00 (CEST) |

Variant on transcripts
|