Product Details
- SNP ID
-
rs149417339
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.5:134115961 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GCATGTACAAAGAGACCGTCTACTC[C/T]GCCTTCAATCTGCTCATGCATTACC
- Phenotype
-
MIM: 189908
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
TCF7
PubMed Links
Gene Details
- Gene
- TCF7
- Gene Name
- transcription factor 7 (T-cell specific, HMG-box)
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001134851.2 |
118 |
Silent Mutation |
TCC,TCT |
S8S |
NP_001128323.2 |
NM_003202.3 |
118 |
Silent Mutation |
TCC,TCT |
S123S |
NP_003193.2 |
NM_201632.3 |
118 |
Silent Mutation |
TCC,TCT |
S8S |
NP_963963.1 |
NM_201634.3 |
118 |
Silent Mutation |
TCC,TCT |
S8S |
NP_963965.1 |
NM_213648.3 |
118 |
Silent Mutation |
TCC,TCT |
S8S |
NP_998813.1 |
XM_006714678.3 |
118 |
Silent Mutation |
TCC,TCT |
S123S |
XP_006714741.1 |
XM_006714679.3 |
118 |
Silent Mutation |
TCC,TCT |
S123S |
XP_006714742.1 |
XM_006714680.3 |
118 |
Silent Mutation |
TCC,TCT |
S123S |
XP_006714743.1 |
XM_006714682.2 |
118 |
Silent Mutation |
TCC,TCT |
S123S |
XP_006714745.1 |
XM_006714684.2 |
118 |
Silent Mutation |
TCC,TCT |
S123S |
XP_006714747.1 |
XM_006714685.3 |
118 |
Silent Mutation |
TCC,TCT |
S8S |
XP_006714748.1 |
XM_006714686.3 |
118 |
Silent Mutation |
TCC,TCT |
S8S |
XP_006714749.1 |
XM_006714687.3 |
118 |
Intron |
|
|
XP_006714750.1 |
XM_011543604.2 |
118 |
Silent Mutation |
TCC,TCT |
S123S |
XP_011541906.1 |
XM_011543606.1 |
118 |
Silent Mutation |
TCC,TCT |
S123S |
XP_011541908.1 |
XM_011543607.2 |
118 |
Intron |
|
|
XP_011541909.1 |
XM_011543608.2 |
118 |
Intron |
|
|
XP_011541910.1 |
XM_011543609.2 |
118 |
Intron |
|
|
XP_011541911.1 |
XM_011543610.2 |
118 |
UTR 5 |
|
|
XP_011541912.1 |
XM_011543611.2 |
118 |
Intron |
|
|
XP_011541913.1 |
XM_011543612.2 |
118 |
Intron |
|
|
XP_011541914.1 |
XM_011543613.2 |
118 |
UTR 5 |
|
|
XP_011541915.1 |
XM_017009789.1 |
118 |
Silent Mutation |
TCC,TCT |
S8S |
XP_016865278.1 |
XM_017009790.1 |
118 |
Intron |
|
|
XP_016865279.1 |
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