Product Details

SNP ID

rs13400205

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:10123737 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAAATTGTGACTTCCGAACCTCAGG[G/T]GGACCTCTCCAAGGACATTCAGCAC

Phenotype

MIM: 180390

Polymorphism

G/T, Transversion 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	383	Missense Mutation	GGG,GTG	G107V	NP_001025.1
NM_001165931.1	383	Missense Mutation	GGG,GTG	G167V	NP_001159403.1

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