Product Details

SNP ID
rs7284161
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.22:30634852 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTAGCCTGGAATCTGGATGGACCT[A/C]TTCTGCCCTGGGGCGCGCCGTTTAC
Phenotype
MIM: 613441
Polymorphism
A/C, Transversion Substitution
Allele Nomenclature
Literature Links
SLC35E4 PubMed Links
Additional Information
For this assay, SNP(s) [rs114083076] 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
SLC35E4
Gene Name
solute carrier family 35 member E4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001001479.3 705 Intron NP_001001479.1
NM_001318370.1 705 Intron NP_001305299.1
NM_001318371.1 705 Intron NP_001305300.1
XM_017028794.1 705 UTR 5 XP_016884283.1
XM_017028795.1 705 Intron XP_016884284.1
Gene
TCN2
Gene Name
transcobalamin 2
There are no transcripts associated with this gene.

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