Product Details

SNP ID

rs142026539

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:41116234 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CATCTTACTCCTGCTCCTGGCTCTC[A/G]TCTGTCTGCTCCTGACCCTAAGCTC

Phenotype

MIM: 124070

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

CYP2F1 PubMed Links

Additional Information

For this assay, SNP(s) [rs3833221] 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

CYP2F1

Gene Name

cytochrome P450 family 2 subfamily F member 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000774.4	258	Missense Mutation	ATC,GTC	I16V	NP_000765.2
XM_011526551.2	258	Missense Mutation	ATC,GTC	I16V	XP_011524853.1
XM_011526552.2	258	Missense Mutation	ATC,GTC	I16V	XP_011524854.1
XM_011526553.2	258	Missense Mutation	ATC,GTC	I91V	XP_011524855.1
XM_011526554.2	258	Intron			XP_011524856.1
XM_011526555.2	258	Missense Mutation	ATC,GTC	I91V	XP_011524857.1
XM_017026384.1	258	Missense Mutation	ATC,GTC	I91V	XP_016881873.1
XM_017026385.1	258	Missense Mutation	ATC,GTC	I91V	XP_016881874.1
XM_017026386.1	258	Missense Mutation	ATC,GTC	I91V	XP_016881875.1
XM_017026387.1	258	Missense Mutation	ATC,GTC	I91V	XP_016881876.1

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