Product Details

SNP ID

rs7965910

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:100283182 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AATTCAGCATCCACTTGGAAAAAAC[A/C]CACATGCTAAGAACCATAAAATGCA

Phenotype

MIM: 616365

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

SCYL2 PubMed Links

Additional Information

For this assay, SNP(s) [rs75218007,rs78157199] 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

SCYL2

Gene Name

SCY1 like pseudokinase 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001317784.1		Intron			NP_001304713.1
NM_017988.5		Intron			NP_060458.3
XM_017019618.1		Intron			XP_016875107.1
XM_017019619.1		Intron			XP_016875108.1
XM_017019620.1		Intron			XP_016875109.1

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