Product Details

SNP ID

rs79378816

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:42764001 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGTGTAAGGTGTAGGATCCTGCGTC[C/T]TCCTGGGTGACATTCTGGATCAGCA

Phenotype

MIM: 176397

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

PSG8 PubMed Links

Additional Information

For this assay, SNP(s) [rs77134863] are located under a probe and SNP(s) [rs7256456] 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

PSG8

Gene Name

pregnancy specific beta-1-glycoprotein 8

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001130167.1	443	Silent Mutation	GAA,GAG	E115E	NP_001123639.1
NM_001130168.1	443	Intron			NP_001123640.1
NM_182707.2	443	Silent Mutation	GAA,GAG	E115E	NP_874366.1
XM_011526986.1	443	Intron			XP_011525288.1
XM_011526987.2	443	Intron			XP_011525289.1
XM_011526988.2	443	Intron			XP_011525290.1

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