Product Details

SNP ID

rs180805457

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:152648905 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCTTTCTGCATTATAGTTTGTGTCG[C/T]TGCAAAAAGAACCAGGCGATAGTCA

Phenotype

MIM: 600375

Polymorphism

C/T, 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	666	Missense Mutation	ACG,GCG	T194A	NP_005422.1

View Full Product Details