Product Details

SNP ID

rs11229651

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.11:58834836 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

AAGAACATGTTTGAAAAGTTTCCTT[C/T]CCTGTGAAGAAAAAGAATTTTACAT

Phenotype

MIM: 614762

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

GLYATL2 PubMed Links

Additional Information

For this assay, SNP(s) [rs111235124] 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

GLYATL2

Gene Name

glycine-N-acyltransferase like 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_145016.3	794	Missense Mutation	AAA,GAA	K160E	NP_659453.3
XM_011544809.2	794	Missense Mutation	AAA,GAA	K119E	XP_011543111.1
XM_017017337.1	794	Missense Mutation	AAA,GAA	K160E	XP_016872826.1
XM_017017338.1	794	Missense Mutation	AAA,GAA	K160E	XP_016872827.1

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