Product Details
- SNP ID
-
rs145103345
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.19:41116504 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TACACAGTGCACCTGGGACCCAGGC[A/G]GGTGGTGGTCCTCAGCGGGTACCAA
- Phenotype
-
MIM: 124070
- Polymorphism
- A/G, 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 |
433 |
Missense Mutation |
CAG,CGG |
Q74R |
NP_000765.2 |
XM_011526551.2 |
433 |
Missense Mutation |
CAG,CGG |
Q74R |
XP_011524853.1 |
XM_011526552.2 |
433 |
Missense Mutation |
CAG,CGG |
Q74R |
XP_011524854.1 |
XM_011526553.2 |
433 |
Missense Mutation |
CAG,CGG |
Q149R |
XP_011524855.1 |
XM_011526554.2 |
433 |
Missense Mutation |
CAG,CGG |
Q10R |
XP_011524856.1 |
XM_011526555.2 |
433 |
Missense Mutation |
CAG,CGG |
Q149R |
XP_011524857.1 |
XM_017026384.1 |
433 |
Missense Mutation |
CAG,CGG |
Q149R |
XP_016881873.1 |
XM_017026385.1 |
433 |
Missense Mutation |
CAG,CGG |
Q149R |
XP_016881874.1 |
XM_017026386.1 |
433 |
Missense Mutation |
CAG,CGG |
Q149R |
XP_016881875.1 |
XM_017026387.1 |
433 |
Missense Mutation |
CAG,CGG |
Q149R |
XP_016881876.1 |
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