Product Details

SNP ID

rs12641357

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.4:7197405 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

CTTCCTTTGCATCTCCTGAGTTTAG[A/T]AGTGGATCTTAGAGTAGTCTAGTGG

Phenotype

MIM: 606284

Polymorphism

A/T, Transversion Substitution

Allele Nomenclature

Literature Links

SORCS2 PubMed Links

Additional Information

For this assay, SNP(s) [rs76311699] 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

SORCS2

Gene Name

sortilin related VPS10 domain containing receptor 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_020777.2		Intron			NP_065828.2
XM_005247987.4		Intron			XP_005248044.2
XM_011513514.2		Intron			XP_011511816.1
XM_011513515.2		Intron			XP_011511817.1
XM_011513516.2		Intron			XP_011511818.1
XM_017008481.1		Intron			XP_016863970.1

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