Variant #0000080784 (NC_000010.10:g.96695777_96695778del, NM_000771.3:c.-2663_-2662del (CYP2C9))
| Individual ID |
00051649 |
| Chromosome |
10 |
| Allele |
Parent #1 |
| 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.96695777_96695778del |
| DNA change (hg38) |
g.94936020_94936021del |
| Published as |
- |
| ISCN |
- |
| DB-ID |
CYP2C9_001001 See all 8 reported entries |
| Variant remarks |
- |
| Reference |
PubMed: King 2004 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
0.10 (306 chromosomes) |
| 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 |
2013-03-10 14:08:11 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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