Variant #0000081251 (NC_000010.10:g.?, NC_000010.10(NM_000771.3):c.168+83? (CYP2C9))
| Chromosome |
10 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.? |
| DNA change (hg38) |
- |
| Published as |
IVS1+83 g.-251A>C |
| ISCN |
- |
| DB-ID |
CYP2C9_001038 See all 68 reported entries |
| Variant remarks |
- |
| Reference |
PubMed: Goldestein 2009 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Unknown |
| Segregation |
? |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
| Owner |
Johan den Dunnen |
| Database submission license |
No license selected |
| Created by |
Annemarie Schop (student) |
| Date created |
2013-03-06 10:21:26 +01:00 (CET) |
| Date last edited |
2013-03-08 00:03:02 +01:00 (CET) |
Variant on transcripts
Screenings
|