Product Details
- SNP ID
-
rs148876270
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.10:112950854 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GGCGAACAGGAGGAGAAGAGCTCCG[A/G]AAACTCCTCGGCAGAGAGGGATTTA
- Phenotype
-
MIM: 602228
MIM: 614316
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
TCF7L2
PubMed Links
Gene Details
- Gene
- TCF7L2
- Gene Name
- transcription factor 7 like 2
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001146274.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
NP_001139746.1 |
NM_001146283.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
NP_001139755.1 |
NM_001146284.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
NP_001139756.1 |
NM_001146285.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
NP_001139757.1 |
NM_001146286.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
NP_001139758.1 |
NM_001198525.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
NP_001185454.1 |
NM_001198526.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
NP_001185455.1 |
NM_001198527.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
NP_001185456.1 |
NM_001198528.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
NP_001185457.1 |
NM_001198529.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
NP_001185458.1 |
NM_001198530.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
NP_001185459.1 |
NM_001198531.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
NP_001185460.1 |
NM_030756.4 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
NP_110383.2 |
XM_005270071.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
XP_005270128.1 |
XM_005270075.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
XP_005270132.1 |
XM_005270077.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
XP_005270134.1 |
XM_005270078.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
XP_005270135.1 |
XM_005270079.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
XP_005270136.1 |
XM_005270080.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
XP_005270137.1 |
XM_005270084.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
XP_005270141.1 |
XM_005270085.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
XP_005270142.1 |
XM_005270086.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
XP_005270143.1 |
XM_005270088.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
XP_005270145.1 |
XM_005270089.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
XP_005270146.1 |
XM_005270091.2 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
XP_005270148.1 |
XM_005270092.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
XP_005270149.1 |
XM_005270093.2 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
XP_005270150.1 |
XM_005270094.2 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
XP_005270151.1 |
XM_005270095.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
XP_005270152.1 |
XM_005270096.2 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
XP_005270153.1 |
XM_005270100.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
XP_005270157.1 |
XM_005270101.2 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
XP_005270158.1 |
XM_005270102.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
XP_005270159.1 |
XM_005270103.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
XP_005270160.1 |
XM_005270104.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
XP_005270161.1 |
XM_011540109.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
XP_011538411.1 |
XM_011540110.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
XP_011538412.1 |
XM_011540111.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
XP_011538413.1 |
XM_011540113.2 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
XP_011538415.1 |
XM_011540116.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
XP_011538418.1 |
XM_017016584.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
XP_016872073.1 |
XM_017016585.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
XP_016872074.1 |
XM_017016586.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
XP_016872075.1 |
XM_017016587.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
XP_016872076.1 |
XM_017016588.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
XP_016872077.1 |
XM_017016589.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
XP_016872078.1 |
XM_017016590.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
XP_016872079.1 |
XM_017016591.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
XP_016872080.1 |
XM_017016592.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
XP_016872081.1 |
XM_017016593.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
XP_016872082.1 |
XM_017016594.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
XP_016872083.1 |
XM_017016595.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
XP_016872084.1 |
XM_017016596.1 |
636 |
Missense Mutation |
GAA,GGA |
E33G |
XP_016872085.1 |
- Gene
- VTI1A
- Gene Name
- vesicle transport through interaction with t-SNAREs 1A
There are no transcripts associated with this gene.
View Full Product Details