Product Details

SNP ID

rs181648518

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:15673560 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCTGCTGAGCCTGCCCTGGCTGGGC[C/T]TCAGACCGGTGGCAACGTCCCCATG

Phenotype

MIM: 611485

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

CYP4F12 PubMed Links

Additional Information

For this assay, SNP(s) [rs16995376] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

CYP4F12

Gene Name

cytochrome P450 family 4 subfamily F member 12

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_023944.3	145	Intron			NP_076433.3
XM_006722850.3	145	UTR 5			XP_006722913.1
XM_011528202.2	145	Intron			XP_011526504.1
XM_011528203.2	145	Intron			XP_011526505.1
XM_011528204.2	145	Intron			XP_011526506.1
XM_011528205.2	145	Intron			XP_011526507.1
XM_011528207.2	145	Intron			XP_011526509.1
XM_011528208.2	145	Intron			XP_011526510.1
XM_017027172.1	145	Missense Mutation	CTC,TTC	L11F	XP_016882661.1

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