Variant #0000409909 (NC_000010.10:g.89624218C>G, NM_000314.4:c.-9C>G (PTEN))
| Chromosome |
10 |
| 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.89624218C>G |
| DNA change (hg38) |
g.87864461C>G |
| Published as |
-9C>G |
| ISCN |
- |
| DB-ID |
PTEN_000023 See all 5 reported entries |
| Variant remarks |
- |
| Reference |
copy from ZJU-CGGM database (China) |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00362 View details |
| Owner |
Peikuan Cong |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2013-05-17 12:00:00 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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