Product Details

SNP ID
rs199619994
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:15645814 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGTGGGTGGGGCCCTGGCACGCAAT[C/T]GTCCGCATCTTCCACCCCACCTACA
Phenotype
MIM: 601270
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
CYP4F3 PubMed Links

Gene Details

Gene
CYP4F3
Gene Name
cytochrome P450 family 4 subfamily F member 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000896.2 96 Silent Mutation ATC,ATT I98I NP_000887.2
NM_001199208.1 96 Intron NP_001186137.1
NM_001199209.1 96 Intron NP_001186138.1
XM_005259911.4 96 Intron XP_005259968.1
XM_011528014.2 96 UTR 5 XP_011526316.1
XM_017026814.1 96 Intron XP_016882303.1
XM_017026815.1 96 Intron XP_016882304.1

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