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- SNP ID:
- rs915437095
- Gene
-
FBXW7 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.4: 152352409 - 152352409 on Build GRCh38
- Polymorphism:
- C/T, Transition substitution
- Context Sequence [VIC/FAM]:
CAGCCATCTCTGATGATACAGATTT[C/T]CCTTCTCAGGCAGGCATACACACAC
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606278
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Literature Links: |
FBXW7 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap |
|---|---|---|
| Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
| EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
| SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
| AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
| EUR - Not Available | ||
| AMR - Not Available |
| FBXW7 - F-box and WD repeat domain containing 7 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001013415.1 | Intron | NP_001013433.1 | ||||
| NM_001257069.1 | Intron | NP_001243998.1 | ||||
| NM_018315.4 | Intron | NP_060785.2 | ||||
| NM_033632.3 | Intron | NP_361014.1 | ||||
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