Product Details

SNP ID

rs59092606

Assay Type

DME

NCBI dbSNP Submissions

NA

Location

Chr.19:15618122 on Build GRCh38

Set Membership

DME Validated Inventoried

Context Sequence [VIC/FAM]

TCAACTTGTGCCACCCTGACATCGT[C/T]CGATCTGTCATCAATACCTCAGGTA

Phenotype

MIM: 611545

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

CYP4F8 PubMed Links

Gene Details

Gene

CYP4F8

Gene Name

cytochrome P450 family 4 subfamily F member 8

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_007253.3	322	Silent Mutation	GTC,GTT	V107V	NP_009184.1
XM_017026232.1	322	Silent Mutation	GTC,GTT	V107V	XP_016881721.1

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