Product Details

SNP ID

rs488787

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.9:212908 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

AATGTATGTCATAAACATTCAGAAA[C/T]TCAGAGGAGTTCATCCGAAAGGCTG

Phenotype

MIM: 611432

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

C9orf66 PubMed Links

Additional Information

For this assay, SNP(s) [rs77862137] 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

C9orf66

Gene Name

chromosome 9 open reading frame 66

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_152569.2		Intron			NP_689782.2

Gene

DOCK8

Gene Name

dedicator of cytokinesis 8

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001190458.1		Intron			NP_001177387.1
NM_001193536.1		Intron			NP_001180465.1
NM_203447.3		Intron			NP_982272.2
XM_011518045.2		Intron			XP_011516347.1
XM_011518046.2		Intron			XP_011516348.1
XM_011518047.2		Intron			XP_011516349.1
XM_011518048.2		Intron			XP_011516350.1
XM_011518049.2		Intron			XP_011516351.1
XM_017015173.1		Intron			XP_016870662.1
XM_017015174.1		Intron			XP_016870663.1

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