Product Details

SNP ID
rs3813997
Assay Type
Functionally tested
NCBI dbSNP Submissions
17
Location
Chr.1:46961472 on Build GRCh38
Set Membership
HapMap JSNP
Context Sequence [VIC/FAM]
ACACTCACCCACTCTGGTTTGAACC[A/G]TTCACTGGCTTCCAGAACATTTGAG
Phenotype
MIM: 614999
Polymorphism
A/G, 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_001320289.1 109 UTR 5 NP_001307218.1
NM_001320290.1 109 Intron NP_001307219.1
NM_178033.1 109 Intron NP_828847.1
XM_017000973.1 109 Intron XP_016856462.1

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