Product Details

SNP ID

rs17136239

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:656343 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GTTTCCAAGATTTTTAAAATAACTT[C/T]GAATGGACACCACCTCCGTCTCTAT

Phenotype

MIM: 615329 MIM: 609713

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

EXOC2 PubMed Links

Additional Information

For this assay, SNP(s) [rs192257165] 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

EXOC2

Gene Name

exocyst complex component 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_018303.5	622	Intron			NP_060773.3
XM_017011018.1	622	Intron			XP_016866507.1
XM_017011019.1	622	Intron			XP_016866508.1
XM_017011020.1	622	Intron			XP_016866509.1
XM_017011021.1	622	Intron			XP_016866510.1
XM_017011022.1	622	Intron			XP_016866511.1
XM_017011023.1	622	Intron			XP_016866512.1
XM_017011024.1	622	Intron			XP_016866513.1
XM_017011025.1	622	Intron			XP_016866514.1
XM_017011026.1	622	Intron			XP_016866515.1

Gene

HUS1B

Gene Name

HUS1 checkpoint clamp component B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_148959.3	622	Missense Mutation	CAA,CGA	Q201R	NP_683762.2

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