Product Details

SNP ID

rs201138737

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:43268146 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGGCGGGTTCCAGAAGTTTAAAAGT[C/G]ATGCTAGGAGGGGGAGACAGCATCA

Phenotype

MIM: 176398

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

PSG9 PubMed Links

Additional Information

For this assay, SNP(s) [rs3746297] are located under a probe 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	162	Nonsense Mutation	TCA,TGA	S23*	NP_001288636.1
NM_001301708.1	162	Nonsense Mutation	TCA,TGA	S23*	NP_001288637.1
NM_001301709.1	162	Nonsense Mutation	TCA,TGA	S23*	NP_001288638.1
NM_002784.4	162	Nonsense Mutation	TCA,TGA	S23*	NP_002775.3
XM_005259075.3	162	Nonsense Mutation	TCA,TGA	S23*	XP_005259132.1
XM_017027004.1	162	Nonsense Mutation	TCA,TGA	S23*	XP_016882493.1
XM_017027005.1	162	Nonsense Mutation	TCA,TGA	S23*	XP_016882494.1
XM_017027006.1	162	Nonsense Mutation	TCA,TGA	S23*	XP_016882495.1
XM_017027007.1	162	Nonsense Mutation	TCA,TGA	S23*	XP_016882496.1

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