Product Details

SNP ID

rs10468679

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.18:11695677 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATGATTCTTTTCCTGGATTGTTATT[C/T]GAATTTTAAATCCTCAGCTGTAGAT

Phenotype

MIM: 139312

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

GNAL PubMed Links

Additional Information

For this assay, SNP(s) [rs73944205] 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

GNAL

Gene Name

G protein subunit alpha L

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001142339.2		Intron			NP_001135811.1
NM_001261443.1		Intron			NP_001248372.1
NM_001261444.1		Intron			NP_001248373.1
NM_182978.3		Intron			NP_892023.1
XM_006722324.2		Intron			XP_006722387.1

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