Product Details

SNP ID

rs510160

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.13:113168167 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TATTTTTGTTTAAACAGTATCCTGT[A/G]AAGAAGTTTAAAGAATAAGGAAAAA

Phenotype

MIM: 613713 MIM: 176895

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

PCID2 PubMed Links

Additional Information

For this assay, SNP(s) [rs2146750] 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

PCID2

Gene Name

PCI domain containing 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001127202.3		Intron			NP_001120674.1
NM_001127203.3		Intron			NP_001120675.1
NM_001258213.2		Intron			NP_001245142.1
NM_001320655.1		Intron			NP_001307584.1
NM_001320656.1		Intron			NP_001307585.1
NM_001320657.1		Intron			NP_001307586.1
NM_001320659.1		Intron			NP_001307588.1
NM_001320660.1		Intron			NP_001307589.1
NM_018386.4		Intron			NP_060856.2
XM_005268325.3		Intron			XP_005268382.1
XM_017020664.1		Intron			XP_016876153.1
XM_017020665.1		Intron			XP_016876154.1
XM_017020666.1		Intron			XP_016876155.1
XM_017020667.1		Intron			XP_016876156.1
XM_017020668.1		Intron			XP_016876157.1
XM_017020669.1		Intron			XP_016876158.1
XM_017020670.1		Intron			XP_016876159.1
XM_017020671.1		Intron			XP_016876160.1
XM_017020672.1		Intron			XP_016876161.1

Gene

PROZ

Gene Name

protein Z, vitamin K dependent plasma glycoprotein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001256134.1		Intron			NP_001243063.1
NM_003891.2		Intron			NP_003882.1
XM_017020812.1		Intron			XP_016876301.1
XM_017020813.1		Intron			XP_016876302.1

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