Product Details

SNP ID

rs111233577

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:29829667 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACGTGCCATGTGCAGCATGAGGGGC[A/T]GCCGGAGCCCCTCATGCTGAGATGG

Phenotype

MIM: 142871

Polymorphism

A/T, Transversion Substitution

Allele Nomenclature

Literature Links

HLA-G PubMed Links

Additional Information

For this assay, SNP(s) [rs12722482] 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

HLA-G

Gene Name

major histocompatibility complex, class I, G

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002127.5	602	Missense Mutation	CAG,CTG	Q290L	NP_002118.1
XM_017010816.1	602	Missense Mutation	CAG,CTG	Q295L	XP_016866305.1
XM_017010817.1	602	Missense Mutation	CAG,CTG	Q198L	XP_016866306.1
XM_017010818.1	602	Missense Mutation	CAG,CTG	Q198L	XP_016866307.1

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