Product Details

SNP ID

rs149099078

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:152648889 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTCTGATGAGCTCGAGGCTTTCTGC[A/G]TTATAGTTTGTGTCGTTGCAAAAAG

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	682	Missense Mutation			NP_005422.1

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