Product Details

SNP ID

rs1739387

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:125782672 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGAAAGTTCGTCAATTTAAATATTT[C/T]TTCTGGCAGGACAACTATCCTAAGT

Phenotype

MIM: 609752

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

NCOA7 PubMed Links

Additional Information

For this assay, SNP(s) [rs116805222] 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

NCOA7

Gene Name

nuclear receptor coactivator 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001122842.2		Intron			NP_001116314.1
NM_001199619.1		Intron			NP_001186548.1
NM_001199620.1		Intron			NP_001186549.1
NM_001199621.1		Intron			NP_001186550.1
NM_001199622.1		Intron			NP_001186551.1
NM_181782.4		Intron			NP_861447.3
XM_005266822.4		Intron			XP_005266879.1
XM_006715340.3		Intron			XP_006715403.1
XM_011535455.2		Intron			XP_011533757.1
XM_017010269.1		Intron			XP_016865758.1
XM_017010270.1		Intron			XP_016865759.1
XM_017010271.1		Intron			XP_016865760.1
XM_017010272.1		Intron			XP_016865761.1
XM_017010273.1		Intron			XP_016865762.1
XM_017010274.1		Intron			XP_016865763.1

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