Product Details

SNP ID

rs9678342

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.2:230418996 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GATCTATAAATCAATTTGAAGAGAA[C/T]GGACATCTTTACATTCACGAGACTT

Phenotype

MIM: 604585

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

SP100 PubMed Links

Additional Information

For this assay, SNP(s) [rs111567440] 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

SP100

Gene Name

SP100 nuclear antigen

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001080391.1		Intron			NP_001073860.1
NM_001206701.1		Intron			NP_001193630.1
NM_001206702.1		Intron			NP_001193631.1
NM_001206703.1		Intron			NP_001193632.1
NM_001206704.1		Intron			NP_001193633.1
NM_003113.3		Intron			NP_003104.2

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