Product Details

SNP ID: rs11959306
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.5:6449193 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TCACGCCGCGCGGCTGGTCCAGCGC[C/T]TACACCGTGGAGGCCGTCATGCGCC
Phenotype: MIM: 615832
Polymorphism: C/T, 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	571	Silent Mutation	GCC,GCT	A100A	NP_001138633.1