Product Details

SNP ID

rs17328447

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.7:87630830 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGGCTTTAGGTCATGTAATGATCA[C/T]GTGTGCCCTTATCAGAGACAGTTGA

Phenotype

MIM: 171050

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

ABCB1 PubMed Links

Additional Information

For this assay, SNP(s) [rs28381767] 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

ABCB1

Gene Name

ATP binding cassette subfamily B member 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000927.4		Intron			NP_000918.2

Gene

RUNDC3B

Gene Name

RUN domain containing 3B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001134405.1		Intron			NP_001127877.1
NM_001134406.1		Intron			NP_001127878.1
NM_138290.2		Intron			NP_612147.1
XM_005250156.2		Intron			XP_005250213.1
XM_005250158.2		Intron			XP_005250215.1
XM_011515826.1		Intron			XP_011514128.1
XM_011515827.1		Intron			XP_011514129.1
XM_011515828.2		Intron			XP_011514130.1
XM_011515829.2		Intron			XP_011514131.1
XM_017011761.1		Intron			XP_016867250.1
XM_017011762.1		Intron			XP_016867251.1
XM_017011763.1		Intron			XP_016867252.1
XM_017011764.1		Intron			XP_016867253.1
XM_017011765.1		Intron			XP_016867254.1
XM_017011766.1		Intron			XP_016867255.1

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