Product Details

SNP ID

rs78658157

Assay Type

Functionally Tested

NCBI dbSNP Submissions

12

Location

Chr.1:231338093 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAAGAGTAAAGGCTGAAACTAGCTT[C/G]CTGAAAGCTTCGTAGGGCCCGAGCC

Phenotype

MIM: 615283 MIM: 616086

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

EXOC8 PubMed Links

Additional Information

For this assay, SNP(s) [rs112263680] 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

EXOC8

Gene Name

exocyst complex component 8

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_175876.4	158	Intron			NP_787072.2

Gene

SPRTN

Gene Name

SprT-like N-terminal domain

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001010984.3	158	UTR 5			NP_001010984.1
NM_001261462.2	158	UTR 5			NP_001248391.1
NM_032018.6	158	UTR 5			NP_114407.3
XM_006711818.2	158	UTR 5			XP_006711881.1
XM_011544289.2	158	Intron			XP_011542591.1

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