Product Details

SNP ID

rs2618386

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:12008127 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAACAGGTGTTTATGTTGTTTCTTC[G/T]GTGTGTTATACTCTCACCAGCGAAG

Phenotype

MIM: 600755

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

SYN2 PubMed Links

Additional Information

For this assay, SNP(s) [rs111458568] 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

SYN2

Gene Name

synapsin II

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003178.5		Intron			NP_003169.2
NM_133625.4		Intron			NP_598328.1
XM_006713311.3		Intron			XP_006713374.1
XM_006713312.3		Intron			XP_006713375.1
XM_006713313.2		Intron			XP_006713376.1
XM_017007087.1		Intron			XP_016862576.1

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