Product Details

SNP ID

rs192387833

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:15618079 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCCCAGGGCTTTGTGAGGTGGTTGG[A/G]CCCCATCACTCCCATCATCAACTTG

Phenotype

MIM: 611545

Polymorphism

A/G, 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	279	Missense Mutation	GAC,GGC	D93G	NP_009184.1
XM_017026232.1	279	Missense Mutation	GAC,GGC	D93G	XP_016881721.1

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