Product Details

SNP ID
rs2712366
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.3:113846071 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TATTTTTGGTCATATTTAGAAAAGG[A/T]TTATGACAATATTGTAGTATTATGA
Phenotype
Polymorphism
A/T, Transversion Substitution
Allele Nomenclature
Literature Links
GRAMD1C PubMed Links
Additional Information
For this assay, SNP(s) [rs201758485] 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
GRAMD1C
Gene Name
GRAM domain containing 1C
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001172105.1 Intron NP_001165576.1
NM_017577.4 Intron NP_060047.3
XM_005247546.2 Intron XP_005247603.1
XM_005247547.1 Intron XP_005247604.1
XM_011512930.1 Intron XP_011511232.1
XM_011512931.1 Intron XP_011511233.1
XM_017006646.1 Intron XP_016862135.1
XM_017006647.1 Intron XP_016862136.1
XM_017006648.1 Intron XP_016862137.1
XM_017006649.1 Intron XP_016862138.1

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