Variant #0000409907 (NC_000010.10:g.89623392C>T, NM_000314.4:c.-834C>T (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.89623392C>T |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
- |
| DB-ID |
PTEN_000106 See all 4 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) |
Retrieve |
| 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 |
2020-06-28 14:35:19 +02:00 (CEST) |

Variant on transcripts
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