Product Details

SNP ID: rs12226431
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.11:47784304 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TCTGATGCAGACAGTCTAAGAACCC[A/G]TTTTTGATTTTTAATAGGTGAAACA
Phenotype: MIM: 607614
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: NUP160 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001318399.1		Intron			NP_001305328.1
NM_015231.2		Intron			NP_056046.1