Product Details
- SNP ID
-
rs201678753
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
3
- Location
-
Chr.1:11658540 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CCCTCTGCCTGCCCCCAGCACCTGC[C/T]TCAAGTCCCAGGTGGTGGACCTCAA
- Phenotype
-
MIM: 607112
MIM: 609111
MIM: 605647
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
FBXO2
PubMed Links
Gene Details
- Gene
- FBXO2
- Gene Name
- F-box protein 2
There are no transcripts associated with this gene.
- Gene
- FBXO44
- Gene Name
- F-box protein 44
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001014765.1 |
499 |
Missense Mutation |
CTC,TTC |
L134F |
NP_001014765.1 |
NM_001304790.1 |
499 |
Intron |
|
|
NP_001291719.1 |
NM_001304791.1 |
499 |
Missense Mutation |
CTC,TTC |
L134F |
NP_001291720.1 |
NM_033182.5 |
499 |
Missense Mutation |
CTC,TTC |
L134F |
NP_149438.2 |
NM_183412.2 |
499 |
Intron |
|
|
NP_904319.1 |
NM_183413.2 |
499 |
Intron |
|
|
NP_904320.1 |
XM_005263535.1 |
499 |
Missense Mutation |
CCT,CTT |
P124L |
XP_005263592.1 |
XM_005263536.4 |
499 |
Missense Mutation |
CCT,CTT |
P124L |
XP_005263593.1 |
XM_005263537.1 |
499 |
Missense Mutation |
CCT,CTT |
P124L |
XP_005263594.1 |
XM_006711043.2 |
499 |
Missense Mutation |
CCT,CTT |
P124L |
XP_006711106.1 |
XM_006711045.2 |
499 |
Missense Mutation |
CTC,TTC |
L134F |
XP_006711108.1 |
XM_011542435.1 |
499 |
Missense Mutation |
CCT,CTT |
P124L |
XP_011540737.1 |
XM_017002842.1 |
499 |
Missense Mutation |
CCT,CTT |
P124L |
XP_016858331.1 |
XM_017002843.1 |
499 |
Missense Mutation |
CTC,TTC |
L134F |
XP_016858332.1 |
XM_017002844.1 |
499 |
Intron |
|
|
XP_016858333.1 |
- Gene
- FBXO6
- Gene Name
- F-box protein 6
There are no transcripts associated with this gene.
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