Product Details

SNP ID
rs6512051
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:15673056 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CCAGCCCCGCCTCCTACGGCCTTCC[C/T]TAGATCAGGGGCCAGGGCCAAAGAC
Phenotype
MIM: 611485
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
CYP4F12 PubMed Links

Gene Details

Gene
CYP4F12
Gene Name
cytochrome P450 family 4 subfamily F member 12
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_023944.3 34 Intron NP_076433.3
XM_006722850.3 34 UTR 5 XP_006722913.1
XM_011528202.2 34 Intron XP_011526504.1
XM_011528203.2 34 Intron XP_011526505.1
XM_011528204.2 34 Intron XP_011526506.1
XM_011528205.2 34 Intron XP_011526507.1
XM_011528207.2 34 Intron XP_011526509.1
XM_011528208.2 34 Intron XP_011526510.1
XM_017027172.1 34 Intron XP_016882661.1

View Full Product Details