Product Details

SNP ID

rs914019

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.13:112698597 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATGCTGGGACATCAGGCTGGGAGTC[A/G]AGAGATGGAATTTTAGGCTTTCTCT

Phenotype

MIM: 605868

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

ATP11A PubMed Links

Additional Information

For this assay, SNP(s) [rs76533333] are located under a probe 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

ATP11A

Gene Name

ATPase phospholipid transporting 11A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015205.2		Intron			NP_056020.2
NM_032189.3		Intron			NP_115565.3
XM_005268299.4		Intron			XP_005268356.1
XM_005268300.4		Intron			XP_005268357.1
XM_005268301.4		Intron			XP_005268358.1
XM_005268303.4		Intron			XP_005268360.1
XM_005268305.4		Intron			XP_005268362.1
XM_005268306.4		Intron			XP_005268363.1
XM_011537480.2		Intron			XP_011535782.1
XM_017020490.1		Intron			XP_016875979.1
XM_017020491.1		Intron			XP_016875980.1
XM_017020492.1		Intron			XP_016875981.1

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