Product Details

SNP ID

rs202226401

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:152649008 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGTTCACACTTTCTCCTCCATTGAC[A/G]CGGTCTATCCAGTAAAAAGCTGACA

Phenotype

MIM: 600375

Polymorphism

A/G, Transition 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	563	Silent Mutation	CGC,CGT	R159R	NP_005422.1

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