Product Details

SNP ID

rs28568876

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.15:42512107 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTGAAAACAATTTGTATGATTTTTA[A/T]TTTTTAGGTAATTATTAATATTACT

Phenotype

MIM: 602534

Polymorphism

A/T, Transversion Substitution

Allele Nomenclature

Literature Links

SNAP23 PubMed Links

Additional Information

For this assay, SNP(s) [rs116408563] 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

SNAP23

Gene Name

synaptosome associated protein 23

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003825.3		Intron			NP_003816.2
NM_130798.2		Intron			NP_570710.1
XM_006720725.2		Intron			XP_006720788.1
XM_017022692.1		Intron			XP_016878181.1
XM_017022693.1		Intron			XP_016878182.1
XM_017022694.1		Intron			XP_016878183.1

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