Product Details

SNP ID
rs1913189
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.12:39301330 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CTAAATTCAGTGCCCACATGTACAT[C/G]AGAAAATATGAATAAGACATCTTAA
Phenotype
MIM: 608283
Polymorphism
C/G, Transversion Substitution
Allele Nomenclature
Literature Links
KIF21A PubMed Links
Additional Information
For this assay, SNP(s) [rs74920317] 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
KIF21A
Gene Name
kinesin family member 21A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001173463.1 Intron NP_001166934.1
NM_001173464.1 Intron NP_001166935.1
NM_001173465.1 Intron NP_001166936.1
NM_017641.3 Intron NP_060111.2
XM_005269007.2 Intron XP_005269064.1
XM_005269008.2 Intron XP_005269065.1
XM_005269009.2 Intron XP_005269066.1
XM_005269010.2 Intron XP_005269067.1
XM_005269011.2 Intron XP_005269068.1
XM_005269012.2 Intron XP_005269069.1
XM_005269013.2 Intron XP_005269070.1
XM_005269014.2 Intron XP_005269071.1
XM_006719493.2 Intron XP_006719556.1
XM_006719494.2 Intron XP_006719557.1
XM_011538556.2 Intron XP_011536858.1
XM_017019607.1 Intron XP_016875096.1
XM_017019608.1 Intron XP_016875097.1
XM_017019609.1 Intron XP_016875098.1
XM_017019610.1 Intron XP_016875099.1
XM_017019611.1 Intron XP_016875100.1

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