Product Details

SNP ID

rs2756105

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.10:99787285 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCTCCTTCCCCTTATCCTTAGCAAC[C/T]GCTAAATCTCTTTTCTGTCTTTATA

Phenotype

MIM: 601107

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

ABCC2 PubMed Links

Additional Information

For this assay, SNP(s) [rs7393105] 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

ABCC2

Gene Name

ATP binding cassette subfamily C member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000392.4		Intron			NP_000383.1
XM_006717630.3		Intron			XP_006717693.1
XM_006717631.3		Intron			XP_006717694.1
XM_011539291.2		Intron			XP_011537593.1
XM_017015675.1		Intron			XP_016871164.1

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