Variant #0000245355 (NC_000001.10:g.155113104G>T, NM_018973.3:c.-298C>A (DPM3))
| Chromosome |
1 |
| 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.155113104G>T |
| DNA change (hg38) |
g.155140628G>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
DPM3_000003 |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs4971073 |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
0.14-0.92 |
| 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 |
2010-04-16 20:05:12 +02:00 (CEST) |
| Date last edited |
2018-01-14 21:40:10 +01:00 (CET) |

Variant on transcripts
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