Product Details

SNP ID
rs17102905
Assay Type
Functionally tested
NCBI dbSNP Submissions
17
Location
Chr.1:46969584 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TCATAAATTACTTTTTCTAAAAAAC[G/T]TATTTCTACTATTTACATTGTTTTT
Phenotype
MIM: 614999
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
CYP4X1 PubMed Links

Gene Details

Gene
CYP4X1
Gene Name
cytochrome P450 family 4 subfamily X member 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001320289.1 Intron NP_001307218.1
NM_001320290.1 Intron NP_001307219.1
NM_178033.1 Intron NP_828847.1
XM_017000973.1 Intron XP_016856462.1

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