Product Details

SNP ID

rs6731402

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.2:113711558 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

AAAATTGCAAGTCTATGTGAAAAAT[C/G]AACCTCAATTTATCTAAATGGGATT

Phenotype

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

MIR4782 PubMed Links

Additional Information

For this assay, SNP(s) [rs11298773] 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

MIR4782

Gene Name

microRNA 4782

There are no transcripts associated with this gene.

Gene

SLC35F5

Gene Name

solute carrier family 35 member F5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
XM_005263799.3	5699	UTR 3			XP_005263856.1
XM_011511921.2	5699	UTR 3			XP_011510223.1
XM_011511922.2	5699	UTR 3			XP_011510224.1
XM_011511923.2	5699	UTR 3			XP_011510225.1
XM_017005027.1	5699	Intron			XP_016860516.1
XM_017005028.1	5699	UTR 3			XP_016860517.1

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