Product Details

SNP ID

rs8100017

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:1451275 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GGCTTCGGTCAGCTGAGAAGAACCA[C/T]GTGGGGGAGGCCTGGGTTTGGGGAG

Phenotype

MIM: 612034

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

APC2 PubMed Links

Additional Information

For this assay, SNP(s) [rs8100440] are located under a probe and SNP(s) [rs8100004] 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

APC2

Gene Name

APC2, WNT signaling pathway regulator

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005883.2		Intron			NP_005874.1
XM_005259475.2		Intron			XP_005259532.1
XM_006722607.2		Intron			XP_006722670.1
XM_006722608.3		Intron			XP_006722671.2
XM_006722609.3		Intron			XP_006722672.1
XM_006722610.3		Intron			XP_006722673.2

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