Product Details

SNP ID

rs4818592

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.21:20999767 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGTATTGCTCGTTTGGTCCAGCAGG[C/G]GGTGGTAGAACTCCATTTTAAGCCC

Phenotype

MIM: 602040

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

NCAM2 PubMed Links

Additional Information

For this assay, SNP(s) [rs78786172] 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

NCAM2

Gene Name

neural cell adhesion molecule 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004540.3		Intron			NP_004531.2
XM_011529575.2		Intron			XP_011527877.1
XM_011529576.2		Intron			XP_011527878.1
XM_011529579.2		Intron			XP_011527881.1
XM_011529580.2		Intron			XP_011527882.1
XM_011529581.2		Intron			XP_011527883.1
XM_011529582.2		Intron			XP_011527884.1
XM_011529585.2		Intron			XP_011527887.1
XM_017028353.1		Intron			XP_016883842.1
XM_017028354.1		Intron			XP_016883843.1
XM_017028355.1		Intron			XP_016883844.1
XM_017028356.1		Intron			XP_016883845.1
XM_017028357.1		Intron			XP_016883846.1
XM_017028358.1		Intron			XP_016883847.1

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