Product Details

SNP ID
rs2712135
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:168498698 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AACAAAGATTGAACAAAGTATCTTC[A/G]ACTAAAATTTCTAACTGTTAAATCA
Phenotype
MIM: 608092
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
PALLD PubMed Links

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

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