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
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