Product Details

SNP ID

rs73267808

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.7:1471637 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGTCTATGTCACTCAGAACCTCCAG[C/T]AGATCTGACACAGAGAGAGGGCCAG

Phenotype

MIM: 611345

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

INTS1 PubMed Links

Additional Information

For this assay, SNP(s) [rs201643960] are located under a probe and SNP(s) [rs201643960] 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

INTS1

Gene Name

integrator complex subunit 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001080453.2	6290	Silent Mutation	CTA,CTG	L2063L	NP_001073922.2
XM_011515260.1	6290	Silent Mutation	CTA,CTG	L2073L	XP_011513562.1
XM_011515262.2	6290	Intron			XP_011513564.1
XM_017011959.1	6290	Silent Mutation	CTA,CTG	L2073L	XP_016867448.1
XM_017011960.1	6290	Silent Mutation	CTA,CTG	L2063L	XP_016867449.1

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