Product Details

SNP ID

rs146901255

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:43267808 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAGTATAAGGTGAAGGTGAAATGTC[A/G]AATTTCTTCTCTAGTCTCATCACCT

Phenotype

MIM: 176398

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

PSG9 PubMed Links

Additional Information

For this assay, SNP(s) [rs138808565] 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

PSG9

Gene Name

pregnancy specific beta-1-glycoprotein 9

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001301707.1	500	Missense Mutation			NP_001288636.1
NM_001301708.1	500	Missense Mutation			NP_001288637.1
NM_001301709.1	500	Missense Mutation			NP_001288638.1
NM_002784.4	500	Missense Mutation			NP_002775.3
XM_005259075.3	500	Nonsense Mutation			XP_005259132.1
XM_017027004.1	500	Nonsense Mutation			XP_016882493.1
XM_017027005.1	500	Nonsense Mutation			XP_016882494.1
XM_017027006.1	500	Nonsense Mutation			XP_016882495.1
XM_017027007.1	500	Nonsense Mutation			XP_016882496.1

View Full Product Details