Product Details

SNP ID

rs200398730

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:94687884 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCTGATTGATCATGGAGAGGAGTTT[C/T]CTGGAAGAGGAAGTTTTCCAGTGGC

Phenotype

MIM: 601131

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

CYP2C18 PubMed Links

Gene Details

Gene

CYP2C18

Gene Name

cytochrome P450 family 2 subfamily C member 18

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000772.2	609	Missense Mutation	CCT,TCT	P95S	NP_000763.1
NM_001128925.1	609	Missense Mutation	CCT,TCT	P95S	NP_001122397.1

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