Product Details

SNP ID: rs149660655
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.18:47160803 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GCTTCCAAAACATGCTCTAGCCTGC[C/T]AGGAGGACATATCTTTTTTCCCCTT
Phenotype: MIM: 609382
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: IER3IP1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_016097.4		Intron			NP_057181.1