Product Details

SNP ID

rs4581406

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.11:46940900 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

GTTCCTTGGGTGTTTGCTGTTTGAA[C/T]TTTATGTCTCAAAGGCTTGGCAGAT

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

C11orf49 PubMed Links

Additional Information

For this assay, SNP(s) [rs6485713] 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

C11orf49

Gene Name

chromosome 11 open reading frame 49

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001003676.2		Intron			NP_001003676.1
NM_001003677.2		Intron			NP_001003677.1
NM_001003678.2		Intron			NP_001003678.1
NM_001278222.1		Intron			NP_001265151.1
NM_024113.4		Intron			NP_077018.1
XM_006718315.1		Intron			XP_006718378.1
XM_011520364.2		Intron			XP_011518666.1
XM_011520365.2		Intron			XP_011518667.1
XM_017018276.1		Intron			XP_016873765.1
XM_017018277.1		Intron			XP_016873766.1
XM_017018278.1		Intron			XP_016873767.1
XM_017018279.1		Intron			XP_016873768.1
XM_017018280.1		Intron			XP_016873769.1
XM_017018281.1		Intron			XP_016873770.1
XM_017018282.1		Intron			XP_016873771.1

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