Product Details

SNP ID

rs17406869

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:43010018 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGCTGCTACGTTGGATTATTGAAAG[C/G]AAAAGTTCCTAATCCTGGAGGAGCT

Phenotype

MIM: 176401

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

PSG11 PubMed Links

Additional Information

For this assay, SNP(s) [rs145080050] 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

PSG11

Gene Name

pregnancy specific beta-1-glycoprotein 11

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001113410.1	729	Missense Mutation			NP_001106881.1
NM_002785.2	729	Missense Mutation			NP_002776.3
NM_203287.1	729	Missense Mutation			NP_976032.2

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