Product Details

SNP ID

rs10981010

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.9:111687923 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGAGGTTATGTGTTTAGGAATCTAT[C/T]TGTAAATTCATGTCTTTAAAGGCAT

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

C9orf84 PubMed Links

Additional Information

For this assay, SNP(s) [rs79666487] 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

C9orf84

Gene Name

chromosome 9 open reading frame 84

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001080551.2		Intron			NP_001074020.2
NM_173521.4		Intron			NP_775792.4
XM_006716974.2		Intron			XP_006717037.1
XM_006716975.2		Intron			XP_006717038.1
XM_011518302.2		Intron			XP_011516604.1
XM_011518303.1		Intron			XP_011516605.1
XM_011518306.1		Intron			XP_011516608.1
XM_011518309.1		Intron			XP_011516611.1
XM_017014340.1		Intron			XP_016869829.1
XM_017014341.1		Intron			XP_016869830.1

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