Product Details

SNP ID: rs11689073
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.2:117815820 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: ATTCTCAGGTACAGTCATGCATCGC[A/G]TAACAGGAGGGGGGATACATTGTGA
Phenotype: MIM: 606355
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: DDX18 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006773.3		Intron			NP_006764.3