Product Details

SNP ID: rs201931730
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.4:70689135 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TCCCGAGGCCGGCAGAGTCAACAGG[A/C]GGCAGAGGAGGAGGAAAGAGAGGAG
Phenotype: MIM: 611614
Polymorphism: A/C, Transversion 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	657	Missense Mutation	GAG,GCG	E153A	NP_065101.1