Product Details

SNP ID

rs142985033

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:94688167 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGAAAGAGATGGAAGGAGATCCGGC[A/G]TTTCTGCCTCATGACTCTGCGGAAT

Phenotype

MIM: 601131

Polymorphism

A/G, 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	700	Missense Mutation	CAT,CGT	H125R	NP_000763.1
NM_001128925.1	700	Missense Mutation	CAT,CGT	H125R	NP_001122397.1

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