Product Details

SNP ID
rs28446721
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.7:6595572 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GTGATACCCATTTGCCTGAGGTGCA[A/G]TGGTCCAAGTGGCAGGCAGCCCAGA
Phenotype
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
C7orf26 PubMed Links
Additional Information
For this assay, SNP(s) [rs114855642] 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
C7orf26
Gene Name
chromosome 7 open reading frame 26
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001303039.1 Intron NP_001289968.1
NM_024067.3 Intron NP_076972.2
XM_005249845.4 Intron XP_005249902.1
XM_011515518.2 Intron XP_011513820.1
XM_017012614.1 Intron XP_016868103.1
XM_017012615.1 Intron XP_016868104.1
Gene
ZDHHC4
Gene Name
zinc finger DHHC-type containing 4
There are no transcripts associated with this gene.

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