Product Details

SNP ID

rs143813756

Assay Type

Functionally Tested

NCBI dbSNP Submissions

3

Location

Chr.1:153775684 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGCCGCCGACCCGGAAGGTCCCGAG[G/T]GGGGCTGCAGCCTGGCCTGGCGCCT

Phenotype

MIM: 611347 MIM: 604193

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

INTS3 PubMed Links

Additional Information

For this assay, SNP(s) [rs34527123] are located under a probe and SNP(s) [rs36064263] 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

INTS3

Gene Name

integrator complex subunit 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001324475.1	393	Intron			NP_001311404.1
NM_023015.4	393	Intron			NP_075391.3
XM_005245459.2	393	Intron			XP_005245516.1
XM_005245461.2	393	Intron			XP_005245518.1
XM_006711490.3	393	Intron			XP_006711553.1
XM_011509906.2	393	Intron			XP_011508208.1
XM_017002132.1	393	Intron			XP_016857621.1

Gene

SLC27A3

Gene Name

solute carrier family 27 member 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001317929.1	393	Missense Mutation	GGG,TGG	G110W	NP_001304858.1
NM_024330.1	393	Missense Mutation	GGG,TGG	G110W	NP_077306.1

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