Product Details

SNP ID

rs12516635

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.5:75853804 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CATTACGTTCTTTTCCTAAATTTTG[A/T]AAAGACTGAGTCTTTGAGACCATTT

Phenotype

MIM: 610291

Polymorphism

A/T, Transversion Substitution

Allele Nomenclature

Literature Links

SV2C PubMed Links

Additional Information

For this assay, SNP(s) [rs78995753] 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

SV2C

Gene Name

synaptic vesicle glycoprotein 2C

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001297716.1		Intron			NP_001284645.1
NM_014979.3		Intron			NP_055794.3
XM_011543281.2		Intron			XP_011541583.1
XM_011543282.2		Intron			XP_011541584.2
XM_017009244.1		Intron			XP_016864733.1

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