Product Details

SNP ID

rs77668226

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:85134729 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCCTCCAGAATTCTTCGCCTGCACC[A/G]AAGGAAACTTGGATTTGTGCCCGCT

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		Intron			NP_112573.1
XM_006712109.2		Intron			XP_006712172.1

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