Product Details

SNP ID

rs1053652

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.2:112652260 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GTCAGATGTTTAGATAAGATGGTTG[C/G]CGTACGCATAGTCTGCATGTTGTAT

Phenotype

MIM: 137570

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

FLJ42351 PubMed Links

Additional Information

For this assay, SNP(s) [rs115480286] 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

FLJ42351

Gene Name

uncharacterized LOC400999

There are no transcripts associated with this gene.

Gene

SLC20A1

Gene Name

solute carrier family 20 member 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005415.4		Intron			NP_005406.3
XM_017004768.1		Intron			XP_016860257.1
XM_017004769.1		Intron			XP_016860258.1
XM_017004770.1		Intron			XP_016860259.1
XM_017004771.1		Intron			XP_016860260.1

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