Product Details

SNP ID: rs4701732
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.5:6454549 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GAGGAGAAACAATTCAGCCCATAAC[A/G]CAACCAAACAGGCATTTCTTAACCA
Phenotype: MIM: 615832
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: UBE2QL1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001145161.2		Intron			NP_001138633.1