Product Details

SNP ID

rs388371

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.22:21666405 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

TTCTGCCCGGACCGTCCCCCGTCTG[C/T]TCGCGAGTTTCGCCCTTGAATGAGT

Phenotype

MIM: 607588

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

LOC107985532 PubMed Links

Additional Information

For this assay, SNP(s) [rs75281100] 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

LOC107985532

Gene Name

uncharacterized LOC107985532

There are no transcripts associated with this gene.

Gene

PPIL2

Gene Name

peptidylprolyl isomerase like 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001317996.1		Intron			NP_001304925.1
NM_014337.3		Intron			NP_055152.1
NM_148175.2		Intron			NP_680480.1
NM_148176.2		Intron			NP_680481.1
XM_005261448.3		Intron			XP_005261505.1
XM_011530041.2		Intron			XP_011528343.1
XM_011530042.2		Intron			XP_011528344.1
XM_011530043.2		Intron			XP_011528345.1
XM_011530044.2		Intron			XP_011528346.1
XM_011530046.2		Intron			XP_011528348.1
XM_011530047.2		Intron			XP_011528349.1
XM_011530049.2		Intron			XP_011528351.1
XM_011530050.2		Intron			XP_011528352.1
XM_011530051.2		Intron			XP_011528353.1
XM_017028705.1		Intron			XP_016884194.1
XM_017028706.1		Intron			XP_016884195.1

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