Product Details

SNP ID

rs141990819

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:47216338 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AATATGTCTGTTCTGCTTGGCAGGT[C/G]CTAGCAGAAGATGTGACTCAGACTG

Phenotype

MIM: 600811

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

DDB2 PubMed Links

Gene Details

Gene

DDB2

Gene Name

damage specific DNA binding protein 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000107.2	325	Missense Mutation	CCT,GCT	P44A	NP_000098.1
NM_001300734.1	325	Missense Mutation	CCT,GCT	P44A	NP_001287663.1

View Full Product Details