Product Details

SNP ID

rs28368645

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.2:204553868 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATAAGTGGGAGTTCTCACTGACACA[A/G]AGGACTTCAGGGACTCAGGGAGAAA

Phenotype

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

PARD3B PubMed Links

Additional Information

For this assay, SNP(s) [rs201889009,rs75613285] 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

PARD3B

Gene Name

par-3 family cell polarity regulator beta

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001302769.1		Intron			NP_001289698.1
NM_057177.6		Intron			NP_476518.4
NM_152526.5		Intron			NP_689739.4
NM_205863.3		Intron			NP_995585.2
XM_011510552.2		Intron			XP_011508854.1
XM_011510553.2		Intron			XP_011508855.1
XM_017003283.1		Intron			XP_016858772.1
XM_017003284.1		Intron			XP_016858773.1
XM_017003285.1		Intron			XP_016858774.1
XM_017003286.1		Intron			XP_016858775.1
XM_017003287.1		Intron			XP_016858776.1
XM_017003288.1		Intron			XP_016858777.1
XM_017003289.1		Intron			XP_016858778.1
XM_017003290.1		Intron			XP_016858779.1
XM_017003291.1		Intron			XP_016858780.1
XM_017003292.1		Intron			XP_016858781.1
XM_017003293.1		Intron			XP_016858782.1
XM_017003294.1		Intron			XP_016858783.1

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