Product Details

SNP ID

rs737115

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:134115735 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTAGGGGCCACCTCGGGGAGGCCTG[C/T]CCTCCAGGTCCTTCCCCTAAAACTT

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	129	Intron			NP_001128323.2
NM_003202.3	129	Intron			NP_003193.2
NM_201632.3	129	Intron			NP_963963.1
NM_201634.3	129	Intron			NP_963965.1
NM_213648.3	129	UTR 5			NP_998813.1
XM_006714678.3	129	Intron			XP_006714741.1
XM_006714679.3	129	Intron			XP_006714742.1
XM_006714680.3	129	Intron			XP_006714743.1
XM_006714682.2	129	Intron			XP_006714745.1
XM_006714684.2	129	Intron			XP_006714747.1
XM_006714685.3	129	Intron			XP_006714748.1
XM_006714686.3	129	Intron			XP_006714749.1
XM_006714687.3	129	Intron			XP_006714750.1
XM_011543604.2	129	Intron			XP_011541906.1
XM_011543606.1	129	Intron			XP_011541908.1
XM_011543607.2	129	Intron			XP_011541909.1
XM_011543608.2	129	Intron			XP_011541910.1
XM_011543609.2	129	Intron			XP_011541911.1
XM_011543610.2	129	Intron			XP_011541912.1
XM_011543611.2	129	Intron			XP_011541913.1
XM_011543612.2	129	Intron			XP_011541914.1
XM_011543613.2	129	Intron			XP_011541915.1
XM_017009789.1	129	Intron			XP_016865278.1
XM_017009790.1	129	Intron			XP_016865279.1

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