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SNP ID

rs141338395

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:15879888 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACATGGTCAGGAAGGGCAAATGGGC[C/T]AGGTCGTCCCTAAGGAAACACCCCA

Phenotype

MIM: 604426

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

CYP4F2 PubMed Links

Gene Details

Gene

CYP4F2

Gene Name

cytochrome P450 family 4 subfamily F member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001082.4		Intron			NP_001073.3

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