Product Details

SNP ID

rs116926023

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.18:48546588 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAAATCCCCAGGGATCTCAGGCAGT[A/G]TGGACGGTGAGCTCCAGCTGAGGCT

Phenotype

MIM: 613178

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

CTIF PubMed Links

Additional Information

For this assay, SNP(s) [rs140690518] 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

CTIF

Gene Name

cap binding complex dependent translation initiation factor

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001142397.1		Intron			NP_001135869.1
NM_014772.2		Intron			NP_055587.1
XM_005258392.4		Intron			XP_005258449.1
XM_006722583.3		Intron			XP_006722646.1
XM_006722586.3		Intron			XP_006722649.1
XM_006722587.3		Intron			XP_006722650.1
XM_006722588.3		Intron			XP_006722651.1
XM_006722589.3		Intron			XP_006722652.1
XM_011526278.2		Intron			XP_011524580.1
XM_011526279.2		Intron			XP_011524581.1
XM_017026100.1		Intron			XP_016881589.1
XM_017026101.1		Intron			XP_016881590.1
XM_017026102.1		Intron			XP_016881591.1

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