Product Details

SNP ID
rs6758117
Assay Type
Validated
NCBI dbSNP Submissions
NA
Location
Chr.2:176082509 on Build GRCh38
Set Membership
Validated
Context Sequence [VIC/FAM]
TGTAGGACCAACAGCCCGGCGCTGG[C/T]GCTGCGCGCGGATCGGGGAAGCCCC
Phenotype
MIM: 142991 MIM: 142989
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
EVX2 PubMed Links
Additional Information
For this assay, SNP(s) [rs72919090] 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
EVX2
Gene Name
even-skipped homeobox 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001080458.1 Intron NP_001073927.1
Gene
HOXD13
Gene Name
homeobox D13
There are no transcripts associated with this gene.

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