Product Details

SNP ID

rs141562718

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.22:16964821 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGAGTCTGTGTTGGTGATGCTCTGC[A/G]TGGAGATGGGGTGTTGGGAGGAGCT

Phenotype

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

GAB4 PubMed Links

Additional Information

For this assay, SNP(s) [rs5992599] 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

GAB4

Gene Name

GRB2 associated binding protein family member 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001037814.1	819	Missense Mutation	AAG,AGG	K474R	NP_001032903.1
XM_011546114.2	819	Missense Mutation	AAG,AGG	K321R	XP_011544416.1
XM_011546115.1	819	Missense Mutation	AAG,AGG	K250R	XP_011544417.1
XM_011546116.2	819	Intron			XP_011544418.1
XM_011546117.1	819	Missense Mutation	AAG,AGG	K232R	XP_011544419.1
XM_017028575.1	819	Missense Mutation	AAG,AGG	K474R	XP_016884064.1
XM_017028576.1	819	Missense Mutation	AAG,AGG	K241R	XP_016884065.1

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