Product Details

SNP ID

rs74472037

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.8:22374598 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCTGAGAGGGAGCAGCAAGTGAGGT[A/G]GCTGGAAATGTACGTTGGGTCTAGG

Phenotype

MIM: 608736

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

SLC39A14 PubMed Links

Additional Information

For this assay, SNP(s) [rs535825229] are located under a probe 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

SLC39A14

Gene Name

solute carrier family 39 member 14

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001128431.2		Intron			NP_001121903.1
NM_001135153.1		Intron			NP_001128625.1
NM_001135154.1		Intron			NP_001128626.1
NM_015359.4		Intron			NP_056174.2
XM_005273465.2		Intron			XP_005273522.1
XM_005273466.4		Intron			XP_005273523.1
XM_006716323.2		Intron			XP_006716386.1
XM_006716324.2		Intron			XP_006716387.1
XM_011544478.2		Intron			XP_011542780.1
XM_017013292.1		Intron			XP_016868781.1
XM_017013293.1		Intron			XP_016868782.1
XM_017013294.1		Intron			XP_016868783.1
XM_017013295.1		Intron			XP_016868784.1

View Full Product Details