Product Details

SNP ID
rs741188
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.2:20252246 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CCAGACTGGGCAACATAGCGAGACC[A/G]CATCTCTACAAAATATAAACAAAAC
Phenotype
MIM: 607205
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
PUM2 PubMed Links
Additional Information
For this assay, SNP(s) [rs76181841] 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
PUM2
Gene Name
pumilio RNA binding family member 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001282752.1 Intron NP_001269681.1
NM_001282790.1 Intron NP_001269719.1
NM_001282791.1 Intron NP_001269720.1
NM_015317.2 Intron NP_056132.1
XM_005262607.1 Intron XP_005262664.1
XM_005262609.1 Intron XP_005262666.1
XM_005262610.1 Intron XP_005262667.1
XM_006711973.1 Intron XP_006712036.1
XM_006711974.2 Intron XP_006712037.1
XM_006711975.2 Intron XP_006712038.1
XM_011532719.1 Intron XP_011531021.1
XM_011532720.2 Intron XP_011531022.1
XM_011532721.2 Intron XP_011531023.1
XM_011532723.1 Intron XP_011531025.1
XM_011532724.2 Intron XP_011531026.1
XM_011532725.2 Intron XP_011531027.1
XM_017003701.1 Intron XP_016859190.1
XM_017003702.1 Intron XP_016859191.1
XM_017003703.1 Intron XP_016859192.1
XM_017003704.1 Intron XP_016859193.1
XM_017003705.1 Intron XP_016859194.1
XM_017003706.1 Intron XP_016859195.1
XM_017003707.1 Intron XP_016859196.1
XM_017003708.1 Intron XP_016859197.1
XM_017003709.1 Intron XP_016859198.1
XM_017003710.1 Intron XP_016859199.1
XM_017003711.1 Intron XP_016859200.1
XM_017003712.1 Intron XP_016859201.1
XM_017003713.1 Intron XP_016859202.1
XM_017003714.1 Intron XP_016859203.1
XM_017003715.1 Intron XP_016859204.1

View Full Product Details