chr10:94981296:> Detail (hg38) (CYP2C9)

Information

Genome

Assembly Position
hg19 chr10:96,741,053-96,741,053 
hg38 chr10:94,981,296-94,981,296

HGVS

Type Transcript Protein
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

[No Data.]

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
drug response 2008-03-10 no assertion criteria provided germline Detail
drug response 2006-11-20 no assertion criteria provided germline Detail
CIViC
[No Data.]
DisGeNET
[No Data.]
Annotation

Annotations

DescrptionSourceLinks
NM_000771.3(CYP2C9):c.[430C=;1075A=] AND Warfarin response ClinVar Detail
NM_000771.3(CYP2C9):c.[430C>T;1075A=] AND Warfarin response ClinVar Detail
A genome-wide association study confirms VKORC1, CYP2C9, and CYP4F2 as principal genetic determinant... GWAS Catalog Detail

Overlapped Transcript Coordinates

Gene Transcript ID Exon Number Chromosome Start Stop Type Amino Mutation Transcript Position Links

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
Genome
hg38
Position
chr10:94,981,296-94,981,296
Variant Type
snv
Genome browser