Product Details

SNP ID: rs142982822
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.4:70689247 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GTGTCGCCTGGGTTGAGGCCTTTGC[A/G]AAACCAGTGCCTCAGGTAGATGAGG
Phenotype: MIM: 611614
Polymorphism: A/G, 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	769	Silent Mutation	GCA,GCG	A190A	NP_065101.1