Product Details

SNP ID: rs201070267
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.4:70689292 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: ATGAGGCTGAGACACGGGTCGTGAA[A/G]GATTTGGCTAAAGTTTCAGTGAAAG
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	814	Silent Mutation	AAA,AAG	K205K	NP_065101.1