Product Details

SNP ID

rs199584967

Assay Type

Functionally Tested

NCBI dbSNP Submissions

3

Location

Chr.1:151090497 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGAGCAGGTGTTAGCAGGGATGCCC[A/G]GACTAAAGTAGACAGGACCCCCTTG

Phenotype

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

GABPB2 PubMed Links

Additional Information

For this assay, SNP(s) [rs11204774] 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

GABPB2

Gene Name

GA binding protein transcription factor beta subunit 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001323906.1	531	Missense Mutation	CAG,CGG	Q67R	NP_001310835.1
NM_001323907.1	531	Intron			NP_001310836.1
NM_001323908.1	531	Missense Mutation	CAG,CGG	Q67R	NP_001310837.1
NM_001323909.1	531	Missense Mutation	CAG,CGG	Q67R	NP_001310838.1
NM_001323910.1	531	Missense Mutation	CAG,CGG	Q83R	NP_001310839.1
NM_001323911.1	531	Missense Mutation	CAG,CGG	Q67R	NP_001310840.1
NM_001323912.1	531	Intron			NP_001310841.1
NM_001323913.1	531	Intron			NP_001310842.1
NM_144618.2	531	Missense Mutation	CAG,CGG	Q67R	NP_653219.1
XM_017000246.1	531	Missense Mutation	CAG,CGG	Q83R	XP_016855735.1
XM_017000247.1	531	Missense Mutation	CAG,CGG	Q83R	XP_016855736.1
XM_017000248.1	531	Missense Mutation	CAG,CGG	Q79R	XP_016855737.1
XM_017000249.1	531	Missense Mutation	CAG,CGG	Q67R	XP_016855738.1
XM_017000250.1	531	Missense Mutation	CAG,CGG	Q83R	XP_016855739.1
XM_017000251.1	531	Missense Mutation	CAG,CGG	Q79R	XP_016855740.1
XM_017000252.1	531	Intron			XP_016855741.1
XM_017000253.1	531	Missense Mutation	CAG,CGG	Q83R	XP_016855742.1
XM_017000254.1	531	Intron			XP_016855743.1

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