Product Details

SNP ID
rs1393668
Assay Type
Validated
NCBI dbSNP Submissions
38
Location
Chr.1:46970662 on Build GRCh38
Set Membership
HapMap Validated
Context Sequence [VIC/FAM]
AGTGGTAAAAGAGAAATGTGCTGTG[C/T]AGGAATTCTGGGAACAAGTTGACCA
Phenotype
MIM: 614999
Polymorphism
C/T, Transition 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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