Product Details

SNP ID

rs149532033

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:25653387 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTTTATTTTCTCACATTTAGAAAAA[G/T]GTTACATAGAAGAGAAGGAACTCGA

Phenotype

MIM: 609202

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

SCGN PubMed Links

Additional Information

For this assay, SNP(s) [rs60502981] 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

SCGN

Gene Name

secretagogin, EF-hand calcium binding protein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006998.3	291	Missense Mutation	GGT,TGT	G30C	NP_008929.2
XM_017010181.1	291	Intron			XP_016865670.1

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