Product Details

SNP ID

rs1064796

Assay Type

DME

NCBI dbSNP Submissions

NA

Location

Chr.19:15913852 on Build GRCh38

Set Membership

HapMap DME Validated Inventoried

Context Sequence [VIC/FAM]

TCGGCAGGATGCGGAAGTGCAGCAG[C/G]GTGAGCGCCAGGACCACCTTCATCT

Phenotype

MIM: 611517

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

CYP4F11 PubMed Links

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	1913	Silent Mutation	ACC,ACG	T485T	NP_001122404.1
NM_021187.3	1913	Silent Mutation	ACC,ACG	T485T	NP_067010.3

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