Product Details
- SNP ID
-
rs7679116
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.4:152323003 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- CTGATCCGCCACACAACTCCCCCAC[C/T]CCCCCCACTCTCCAATGTGACTAGG
- Phenotype
-
MIM: 606278
- Polymorphism
- C/T, 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 |
2563 |
Missense Mutation |
AGT,GGT |
S550G |
NP_001013433.1 |
| NM_001257069.1 |
2563 |
Intron |
|
|
NP_001243998.1 |
| NM_018315.4 |
2563 |
Missense Mutation |
AGT,GGT |
S588G |
NP_060785.2 |
| NM_033632.3 |
2563 |
Missense Mutation |
AGT,GGT |
S668G |
NP_361014.1 |
| XM_011532083.1 |
2563 |
Missense Mutation |
AGT,GGT |
S668G |
XP_011530385.1 |
| XM_011532084.1 |
2563 |
Missense Mutation |
AGT,GGT |
S668G |
XP_011530386.1 |
| XM_011532085.1 |
2563 |
Missense Mutation |
AGT,GGT |
S668G |
XP_011530387.1 |
| XM_011532086.1 |
2563 |
Missense Mutation |
AGT,GGT |
S640G |
XP_011530388.1 |
| XM_011532087.1 |
2563 |
Missense Mutation |
AGT,GGT |
S640G |
XP_011530389.1 |
| XM_011532088.1 |
2563 |
Missense Mutation |
AGT,GGT |
S501G |
XP_011530390.1 |
| XM_017008362.1 |
2563 |
Missense Mutation |
AGT,GGT |
S668G |
XP_016863851.1 |
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