Variant #0000128819 (NC_000011.9:g.2168147C>T, NM_000612.4:c.-8695G>A (IGF2))
| Chromosome |
11 |
| Allele |
Parent #1 |
| 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.2168147C>T |
| DNA change (hg38) |
g.2146917C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
IGF2_000002 |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs17883917 |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
0.00-0.05 |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2009-08-18 09:11:52 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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