Product Details
- SNP ID
-
rs150039691
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.5:171868641 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CGGGTGAAAGTGCAGACTGTTATCT[A/T]GAGATGTAAGTGTATGTTCTGGAGG
- Phenotype
-
MIM: 605651
- Polymorphism
- A/T, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
FBXW11
PubMed Links
Gene Details
- Gene
- FBXW11
- Gene Name
- F-box and WD repeat domain containing 11
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_012300.2 |
1552 |
Silent Mutation |
TCA,TCT |
S541S |
NP_036432.2 |
| NM_033644.2 |
1552 |
Silent Mutation |
TCA,TCT |
S528S |
NP_387448.2 |
| NM_033645.2 |
1552 |
Silent Mutation |
TCA,TCT |
S507S |
NP_387449.2 |
| XM_005265855.4 |
1552 |
Silent Mutation |
TCA,TCT |
S562S |
XP_005265912.1 |
| XM_005265856.2 |
1552 |
Silent Mutation |
TCA,TCT |
S530S |
XP_005265913.1 |
| XM_005265857.2 |
1552 |
Silent Mutation |
TCA,TCT |
S514S |
XP_005265914.1 |
| XM_005265858.2 |
1552 |
Silent Mutation |
TCA,TCT |
S509S |
XP_005265915.1 |
| XM_017009279.1 |
1552 |
Silent Mutation |
TCA,TCT |
S541S |
XP_016864768.1 |
| XM_017009280.1 |
1552 |
Silent Mutation |
TCA,TCT |
S509S |
XP_016864769.1 |
| XM_017009281.1 |
1552 |
Silent Mutation |
TCA,TCT |
S509S |
XP_016864770.1 |
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