Product Details

SNP ID

rs201200370

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:15673627 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTTGTGGGCTCCTGGCTACTCGCCC[A/G]CATCCTGGCTTGGACCTATGCCTTC

Phenotype

MIM: 611485

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

CYP4F12 PubMed Links

Additional Information

For this assay, SNP(s) [rs16995378] are located under a primer 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	212	Intron			NP_076433.3
XM_006722850.3	212	UTR 5			XP_006722913.1
XM_011528202.2	212	Intron			XP_011526504.1
XM_011528203.2	212	Intron			XP_011526505.1
XM_011528204.2	212	Intron			XP_011526506.1
XM_011528205.2	212	Intron			XP_011526507.1
XM_011528207.2	212	Intron			XP_011526509.1
XM_011528208.2	212	Intron			XP_011526510.1
XM_017027172.1	212	Missense Mutation	CAC,CGC	H33R	XP_016882661.1

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