Product Details

SNP ID: rs181424547
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.20:31303265 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GTAACTGACAAGTTGGAGTTAGAGT[A/C]GTAATCCTCCTTCACATTTTTAGAA
Phenotype
Polymorphism: A/C, Transversion 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	256	Missense Mutation			NP_001032820.1