Product Details

SNP ID

rs10230777

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.7:133258197 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CAGGAAGTCCTGGGATGTCTGGCAG[C/T]ATATGTGAACGTAAGGGGCAACACA

Phenotype

MIM: 608185

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

EXOC4 PubMed Links

Additional Information

For this assay, SNP(s) [rs199676770,rs564128570] 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

EXOC4

Gene Name

exocyst complex component 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001037126.1		Intron			NP_001032203.1
NM_021807.3		Intron			NP_068579.3
XM_005250523.4		Intron			XP_005250580.1
XM_017012494.1		Intron			XP_016867983.1
XM_017012495.1		Intron			XP_016867984.1

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