Product Details

SNP ID

rs11677413

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.2:191953876 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TAGTGCCCAGTTACCTGTAGGGTGC[C/T]GCATTCATTTTTTTTTTTTTTTTTT

Phenotype

MIM: 605734

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

TMEFF2 PubMed Links

Additional Information

For this assay, SNP(s) [rs563154787] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

TMEFF2

Gene Name

transmembrane protein with EGF like and two follistatin like domains 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001305134.1		Intron			NP_001292063.1
NM_001305145.1		Intron			NP_001292074.1
NM_016192.3		Intron			NP_057276.2
XM_011510890.2		Intron			XP_011509192.1
XM_017003739.1		Intron			XP_016859228.1
XM_017003740.1		Intron			XP_016859229.1

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