Product Details

SNP ID
rs6572612
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.14:49775604 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AAGGAGTAGCCAAGATACAGAGATA[C/T]AAGCAAATGTCTTTTTTTTTTTTTT
Phenotype
MIM: 611280 MIM: 608378
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
KLHDC2 PubMed Links
Additional Information
For this assay, SNP(s) [rs8007202] 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
KLHDC2
Gene Name
kelch domain containing 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_014315.2 Intron NP_055130.1
XM_006720094.3 Intron XP_006720157.1
XM_011536610.1 Intron XP_011534912.1
Gene
NEMF
Gene Name
nuclear export mediator factor
There are no transcripts associated with this gene.

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