Product Details

SNP ID
rs10739281
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:109647530 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GTTAGATATTGCCCAGGTGCCTCCG[A/G]AAGTATTGTATCCCTTTACATTGCC
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
PALM2 PubMed Links

Gene Details

Gene
PALM2
Gene Name
paralemmin 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001037293.2 Intron NP_001032370.1
NM_053016.5 Intron NP_443749.5

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