Product Details

SNP ID

rs4841940

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.9:134865366 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GATGGCTTCCAAAAACCCTAGTAGG[C/T]GCCATGGTCTGAGCCTGCTCGTGGT

Phenotype

MIM: 601624

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

FCN2 PubMed Links

Additional Information

For this assay, SNP(s) [rs34733958,rs36027369] 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

FCN2

Gene Name

ficolin 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004108.2		Intron			NP_004099.2
NM_015837.2		Intron			NP_056652.1
XM_006717015.3		Intron			XP_006717078.1
XM_011518392.2		Intron			XP_011516694.1

Gene

LOC101448202

Gene Name

uncharacterized LOC101448202

There are no transcripts associated with this gene.

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