Product Details

SNP ID

rs28393114

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.16:15960927 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGGAAGGCGCTTACCAGCTCAGCAA[C/G]GAAGTAGAACAATGCATGGTCCCTG

Phenotype

MIM: 158343

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

ABCC1 PubMed Links

Additional Information

For this assay, SNP(s) [rs201739093] 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

ABCC1

Gene Name

ATP binding cassette subfamily C member 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004996.3		Intron			NP_004987.2
XM_011522497.1		Intron			XP_011520799.1
XM_011522498.2		Intron			XP_011520800.1
XM_017023237.1		Intron			XP_016878726.1
XM_017023238.1		Intron			XP_016878727.1
XM_017023239.1		Intron			XP_016878728.1
XM_017023240.1		Intron			XP_016878729.1
XM_017023241.1		Intron			XP_016878730.1
XM_017023242.1		Intron			XP_016878731.1
XM_017023243.1		Intron			XP_016878732.1

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