Product Details

SNP ID

rs202025937

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:15914383 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCTTGGTCGAAACGGAAGGGGTCG[C/T]AGACCTGCAGGTGAGACCAAGAAGG

Phenotype

MIM: 611517

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

CYP4F11 PubMed Links

Additional Information

For this assay, SNP(s) [rs12985248] 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

CYP4F11

Gene Name

cytochrome P450 family 4 subfamily F member 11

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001128932.1	1777	Missense Mutation	TAC,TGC	Y440C	NP_001122404.1
NM_021187.3	1777	Missense Mutation	TAC,TGC	Y440C	NP_067010.3

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