Product Details

SNP ID

rs12677346

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.8:94826641 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATTATGTTAAGAGTTAATTTTTTGA[A/G]ATATATTCTGAAATATTTATGGACG

Phenotype

MIM: 611351

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

INTS8 PubMed Links

Additional Information

For this assay, SNP(s) [rs76385021] 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

INTS8

Gene Name

integrator complex subunit 8

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_017864.3		Intron			NP_060334.2
XM_017013616.1		Intron			XP_016869105.1
XM_017013617.1		Intron			XP_016869106.1
XM_017013618.1		Intron			XP_016869107.1
XM_017013619.1		Intron			XP_016869108.1

View Full Product Details