Product Details

SNP ID

rs113827709

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:41116224 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TAAGCACAGCCATCTTACTCCTGCT[C/T]CTGGCTCTCGTCTGTCTGCTCCTGA

Phenotype

MIM: 124070

Polymorphism

C/T, 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	248	Silent Mutation	CTC,CTT	L12L	NP_000765.2
XM_011526551.2	248	Silent Mutation	CTC,CTT	L12L	XP_011524853.1
XM_011526552.2	248	Silent Mutation	CTC,CTT	L12L	XP_011524854.1
XM_011526553.2	248	Silent Mutation	CTC,CTT	L87L	XP_011524855.1
XM_011526554.2	248	Intron			XP_011524856.1
XM_011526555.2	248	Silent Mutation	CTC,CTT	L87L	XP_011524857.1
XM_017026384.1	248	Silent Mutation	CTC,CTT	L87L	XP_016881873.1
XM_017026385.1	248	Silent Mutation	CTC,CTT	L87L	XP_016881874.1
XM_017026386.1	248	Silent Mutation	CTC,CTT	L87L	XP_016881875.1
XM_017026387.1	248	Silent Mutation	CTC,CTT	L87L	XP_016881876.1

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