Product Details

SNP ID: rs17123553
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.20:31305833 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TCATAATAACCTGGCATATTTTTAC[A/G]TATATTCATACTAAGTCTCTAGAAT
Phenotype
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: DEFB116 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001037731.1		Intron			NP_001032820.1