Product Details

SNP ID: rs144519797
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.4:70689043 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CCGTGCAAAGTGAAGCTGAGGCCTC[C/T]GTGGATCCCAGTTTGTCGTGGGGTC
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	565	Silent Mutation	TCC,TCT	S122S	NP_065101.1