Product Details

SNP ID

rs79390284

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.14:57565748 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGTTGGCCTTCTTTTACAAATTCAG[C/T]CATAAGCATTTTAAGAGAATAATAA

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

SLC35F4 PubMed Links

Additional Information

For this assay, SNP(s) [rs139721583] 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

SLC35F4

Gene Name

solute carrier family 35 member F4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001206920.1		Intron			NP_001193849.1
NM_001306087.1		Intron			NP_001293016.1
XM_011536720.2		Intron			XP_011535022.1
XM_011536721.2		Intron			XP_011535023.1
XM_011536723.2		Intron			XP_011535025.1
XM_011536724.2		Intron			XP_011535026.1
XM_011536725.1		Intron			XP_011535027.1
XM_017021258.1		Intron			XP_016876747.1
XM_017021259.1		Intron			XP_016876748.1
XM_017021260.1		Intron			XP_016876749.1
XM_017021261.1		Intron			XP_016876750.1

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