Product Details

SNP ID
rs2712149
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.4:168501554 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AAGCTGCCTGTTGACAATTCAAGGT[C/T]GATAGGATTCTGTAATGACTCACAA
Phenotype
MIM: 608092
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
PALLD PubMed Links
Additional Information
For this assay, SNP(s) [rs117920990] 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
PALLD
Gene Name
palladin, cytoskeletal associated protein
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001166108.1 Intron NP_001159580.1
NM_001166109.1 Intron NP_001159581.1
NM_001166110.1 Intron NP_001159582.1
NM_016081.3 Intron NP_057165.3
XM_005262861.4 Intron XP_005262918.1
XM_005262866.2 Intron XP_005262923.1
XM_011531768.2 Intron XP_011530070.1
XM_011531769.2 Intron XP_011530071.1
XM_011531770.2 Intron XP_011530072.1
XM_011531771.2 Intron XP_011530073.1
XM_011531772.2 Intron XP_011530074.1
XM_011531773.1 Intron XP_011530075.1
XM_011531774.1 Intron XP_011530076.1
XM_011531775.1 Intron XP_011530077.1
XM_017007910.1 Intron XP_016863399.1
XM_017007911.1 Intron XP_016863400.1

View Full Product Details