Product Details

SNP ID: rs199913762
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.4:70689282 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CCTCAGGTAGATGAGGCTGAGACAC[A/G]GGTCGTGAAGGATTTGGCTAAAGTT
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	804	Missense Mutation	CAG,CGG	Q202R	NP_065101.1