Product Details

SNP ID

rs200175007

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:85134030 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCCTCCGCAGGCGGAGAGGCGCCC[A/G]CAGCCCGTCCGGGACACTTTCCAGA

Phenotype

MIM: 604652

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

TCF7L1 PubMed Links

Gene Details

Gene

TCF7L1

Gene Name

transcription factor 7 like 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_031283.2	489	Silent Mutation	CCA,CCG	P88P	NP_112573.1
XM_006712109.2	489	Silent Mutation	CCA,CCG	P88P	XP_006712172.1

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