Product Details

SNP ID
rs4135050
Assay Type
Validated
NCBI dbSNP Submissions
NA
Location
Chr.12:103968698 on Build GRCh38
Set Membership
HapMap Validated
Context Sequence [VIC/FAM]
GGAGAGGCCAGATTAAAGCAGTGTT[A/T]GAGGATTTGTAGCAAATGTAAGGGA
Phenotype
MIM: 601423
Polymorphism
A/T, Transversion Substitution
Allele Nomenclature
Literature Links
C12orf73 PubMed Links
Additional Information
For this assay, SNP(s) [rs4135051] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene
C12orf73
Gene Name
chromosome 12 open reading frame 73
There are no transcripts associated with this gene.

Gene
TDG
Gene Name
thymine DNA glycosylase
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_003211.4 Intron NP_003202.3
XM_005269125.1 Intron XP_005269182.1
XM_011538714.1 Intron XP_011537016.1
XM_011538715.1 Intron XP_011537017.1

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