Product Details

SNP ID

rs3218545

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:152648119 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AAGAAATACTGTTAATTCCCCTAGA[G/T]TTTAAAACTTTAGGGCTGGGCACGG

Phenotype

MIM: 600375

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

XRCC2 PubMed Links

Gene Details

Gene

XRCC2

Gene Name

X-ray repair cross complementing 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005431.1	1452	UTR 3			NP_005422.1

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