Product Details

SNP ID
rs150889173
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.2:10122846 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCGCGCCCATCACGGACCCGCAGCA[A/G]CTGCAGCTCTCGCCGCTGAAGGGGC
Phenotype
MIM: 180390
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
RRM2 PubMed Links

Gene Details

Gene
RRM2
Gene Name
ribonucleotide reductase regulatory subunit M2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001034.3 111 Silent Mutation CAA,CAG Q16Q NP_001025.1
NM_001165931.1 111 Silent Mutation CAA,CAG Q76Q NP_001159403.1

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