Product Details

SNP ID

rs16990421

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.22:32415897 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AAAAAGAAATGGGTCAGTTAAGAGG[C/T]GAGATTTGCATTCTTACCTCAAGAA

Phenotype

MIM: 614109 MIM: 613901

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

BPIFC PubMed Links

Additional Information

For this assay, SNP(s) [rs115332147] 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

BPIFC

Gene Name

BPI fold containing family C

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_174932.2		Intron			NP_777592.1
XM_011530088.2		Intron			XP_011528390.1
XM_011530089.1		Intron			XP_011528391.1
XM_011530090.1		Intron			XP_011528392.1
XM_011530091.2		Intron			XP_011528393.1
XM_017028740.1		Intron			XP_016884229.1

Gene

RTCB

Gene Name

RNA 2',3'-cyclic phosphate and 5'-OH ligase

There are no transcripts associated with this gene.

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