Product Details

SNP ID

rs2355789

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:117914863 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATAGATTCAAGAAGCAGACCTTTTT[C/T]GATGAATACCATTGAGTTTGTTTCA

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

SLC35F1 PubMed Links

Additional Information

For this assay, SNP(s) [rs140332836] 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

SLC35F1

Gene Name

solute carrier family 35 member F1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001029858.3		Intron			NP_001025029.2
XM_005266865.4		Intron			XP_005266922.1

View Full Product Details