Product Details

SNP ID

rs10401260

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:15508800 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGAGGGGCACGTGGGTGTGTCCCCG[A/T]CGTTTGCTGCATTTGTGAGTTGTTT

Phenotype

MIM: 611495

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

CYP4F22 PubMed Links

Gene Details

Gene

CYP4F22

Gene Name

cytochrome P450 family 4 subfamily F member 22

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_173483.3	57	Intron			NP_775754.2
XM_011527692.2	57	Intron			XP_011525994.1
XM_011527693.2	57	UTR 5			XP_011525995.1

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