Product Details

SNP ID

rs145085742

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:152648677 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCAACCCCACTTTCTCCAATAATAA[A/C]AAAATGTTTTTTTAAACTGTTACTT

Phenotype

MIM: 600375

Polymorphism

A/C, 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	894	Missense Mutation	GTT,TTT	V270F	NP_005422.1

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