Product Details

SNP ID: rs16845387
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.4:70688761 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: CAGGTCCCACGCTCACCGACGAAAA[C/T]GGAGATGATTTAGGATTGCCACCCT
Phenotype: MIM: 611614
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: UTP3 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_020368.2	283	Silent Mutation	AAC,AAT	N28N	NP_065101.1