Product Details

SNP ID

rs4076118

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.17:65530976 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGTCCTCTTGGGCCAGGCCCACCCC[C/T]AAACCCCTTCCGAGGAAATTAAGCA

Phenotype

MIM: 604025

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

AXIN2 PubMed Links

Additional Information

For this assay, SNP(s) [rs78226347] are located under a primer 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

AXIN2

Gene Name

axin 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004655.3		Intron			NP_004646.3
XM_011525319.2		Intron			XP_011523621.1
XM_011525320.1		Intron			XP_011523622.1
XM_011525321.2		Intron			XP_011523623.1
XM_017025192.1		Intron			XP_016880681.1
XM_017025193.1		Intron			XP_016880682.1
XM_017025194.1		Intron			XP_016880683.1

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