Product Details

SNP ID

rs6753059

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.2:162332559 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGGAAATCTGAATCAGAATTACTTC[A/G]AAGGATTTTTGCATAACTCATGCCT

Phenotype

MIM: 607030

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

GCA PubMed Links

Additional Information

For this assay, SNP(s) [rs541168521] 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

GCA

Gene Name

grancalcin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
XM_005246446.2		Intron			XP_005246503.1
XM_006712398.3		Intron			XP_006712461.1
XM_006712400.3		Intron			XP_006712463.1
XM_006712401.3		Intron			XP_006712464.1
XM_011510926.2		Intron			XP_011509228.1
XM_011510927.2		Intron			XP_011509229.1
XM_011510928.2		Intron			XP_011509230.1
XM_017003764.1		Intron			XP_016859253.1
XM_017003765.1		Intron			XP_016859254.1
XM_017003766.1		Intron			XP_016859255.1
XM_017003767.1		Intron			XP_016859256.1
XM_017003768.1		Intron			XP_016859257.1
XM_017003769.1		Intron			XP_016859258.1

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