Product Details

SNP ID

rs4918742

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:94915966 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTGGGGACCACTTTTCTGAAACTTC[C/T]TTGTTGCCCAGATGTGGCTAAAAGA

Phenotype

MIM: 601130

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

CYP2C9 PubMed Links

Gene Details

Gene

CYP2C9

Gene Name

cytochrome P450 family 2 subfamily C member 9

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000771.3		Intron			NP_000762.2
XM_017015758.1		Intron			XP_016871247.1

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