Product Details

SNP ID

rs4886697

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.15:75380868 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AAAAGTCCCTTTCTATAAAGACATG[A/G]TTGTTAGTAGGTATTGGAACACGGA

Phenotype

MIM: 607776

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

SIN3A PubMed Links

Additional Information

For this assay, SNP(s) [rs143043200] 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

SIN3A

Gene Name

SIN3 transcription regulator family member A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001145357.1		Intron			NP_001138829.1
NM_001145358.1		Intron			NP_001138830.1
NM_015477.2		Intron			NP_056292.1
XM_006720465.3		Intron			XP_006720528.1
XM_006720466.3		Intron			XP_006720529.1
XM_006720467.3		Intron			XP_006720530.1

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