Product Details

SNP ID
rs140968652
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:41116240 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACTCCTGCTCCTGGCTCTCGTCTGT[C/T]TGCTCCTGACCCTAAGCTCAAGAGA
Phenotype
MIM: 124070
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
CYP2F1 PubMed Links

Gene Details

Gene
CYP2F1
Gene Name
cytochrome P450 family 2 subfamily F member 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000774.4 264 Silent Mutation CTG,TTG L18L NP_000765.2
XM_011526551.2 264 Silent Mutation CTG,TTG L18L XP_011524853.1
XM_011526552.2 264 Silent Mutation CTG,TTG L18L XP_011524854.1
XM_011526553.2 264 Silent Mutation CTG,TTG L93L XP_011524855.1
XM_011526554.2 264 Intron XP_011524856.1
XM_011526555.2 264 Silent Mutation CTG,TTG L93L XP_011524857.1
XM_017026384.1 264 Silent Mutation CTG,TTG L93L XP_016881873.1
XM_017026385.1 264 Silent Mutation CTG,TTG L93L XP_016881874.1
XM_017026386.1 264 Silent Mutation CTG,TTG L93L XP_016881875.1
XM_017026387.1 264 Silent Mutation CTG,TTG L93L XP_016881876.1

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