Product Details

SNP ID
rs147651077
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:10123788 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGGGAATCCCTGAAACCCGAGGAGA[A/G]ATATTTTATATCCCATGTTCTGGCT
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_001034.3 434 Missense Mutation AAA,AGA K124R NP_001025.1
NM_001165931.1 434 Missense Mutation AAA,AGA K184R NP_001159403.1

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