Product Details

SNP ID
rs1273511
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.19:15519008 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GCAACAGATTGGATGTGGCTGAAAG[C/G]GGGAGGAAGAGGGTGAGGTGAATCT
Phenotype
MIM: 611495
Polymorphism
C/G, 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 Intron NP_775754.2
XM_011527692.2 Intron XP_011525994.1
XM_011527693.2 Intron XP_011525995.1

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