Product Details
- SNP ID
-
rs138346992
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.4:152326222 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CCCTAAGAGTGGCATCTCGAGAACC[A/G]CTAACAACTCTGCAGAGGGAGAAAC
- Phenotype
-
MIM: 606278
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
FBXW7
PubMed Links
Gene Details
- Gene
- FBXW7
- Gene Name
- F-box and WD repeat domain containing 7
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001013415.1 |
1989 |
Silent Mutation |
AGC,AGT |
S358S |
NP_001013433.1 |
| NM_001257069.1 |
1989 |
Intron |
|
|
NP_001243998.1 |
| NM_018315.4 |
1989 |
Silent Mutation |
AGC,AGT |
S396S |
NP_060785.2 |
| NM_033632.3 |
1989 |
Silent Mutation |
AGC,AGT |
S476S |
NP_361014.1 |
| XM_011532083.1 |
1989 |
Silent Mutation |
AGC,AGT |
S476S |
XP_011530385.1 |
| XM_011532084.1 |
1989 |
Silent Mutation |
AGC,AGT |
S476S |
XP_011530386.1 |
| XM_011532085.1 |
1989 |
Silent Mutation |
AGC,AGT |
S476S |
XP_011530387.1 |
| XM_011532086.1 |
1989 |
Silent Mutation |
AGC,AGT |
S448S |
XP_011530388.1 |
| XM_011532087.1 |
1989 |
Silent Mutation |
AGC,AGT |
S448S |
XP_011530389.1 |
| XM_011532088.1 |
1989 |
Silent Mutation |
AGC,AGT |
S309S |
XP_011530390.1 |
| XM_017008362.1 |
1989 |
Silent Mutation |
AGC,AGT |
S476S |
XP_016863851.1 |
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