Product Details

SNP ID
rs2460945
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.2:108449832 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGGATCTCAATTTTAGTGTGCGCA[A/G]TCGCCCATTTCCTGTTTCTCCCCCG
Phenotype
MIM: 612711
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
GCC2 PubMed Links
Additional Information
For this assay, SNP(s) [rs78477242] 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
GCC2
Gene Name
GRIP and coiled-coil domain containing 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_181453.3 Intron NP_852118.1
XM_006712870.3 Intron XP_006712933.1
XM_006712871.1 Intron XP_006712934.1
XM_006712872.3 Intron XP_006712935.1
XM_011512213.2 Intron XP_011510515.1

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