Variant #0000454338 (NC_000010.10:g.96702047C>T, NM_000771.3:c.430C>T (CYP2C9))
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.96702047C>T |
DNA change (hg38) |
g.94942290C>T |
Published as |
- |
ISCN |
- |
DB-ID |
CYP2C9_000002 See all 72 reported entries |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs1057910 |
Origin |
Not applicable |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.09261 View details |
Owner |
Hye Sun Gwak |
Database submission license |
No license selected |
Created by |
Hye Sun Gwak |
Date created |
2019-01-28 09:42:29 +01:00 (CET) |
Date last edited |
2019-02-26 16:57:38 +01:00 (CET) |

Variant on transcripts
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