Product Details

SNP ID

rs12456140

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.18:79077760 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TAAGGGGGCCAAACTGAGCCAGCAT[A/G]AGAGAGTCCTCTCTACTTTACCCTG

Phenotype

MIM: 614446

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

ATP9B PubMed Links

Additional Information

For this assay, SNP(s) [rs115653376] 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

ATP9B

Gene Name

ATPase phospholipid transporting 9B (putative)

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001306085.1		Intron			NP_001293014.1
NM_198531.4		Intron			NP_940933.3
XM_011525963.2		Intron			XP_011524265.1
XM_011525964.2		Intron			XP_011524266.1
XM_011525965.2		Intron			XP_011524267.1
XM_011525966.2		Intron			XP_011524268.1
XM_011525971.2		Intron			XP_011524273.2
XM_011525972.2		Intron			XP_011524274.1
XM_011525973.2		Intron			XP_011524275.1
XM_011525974.2		Intron			XP_011524276.1
XM_017025726.1		Intron			XP_016881215.1
XM_017025727.1		Intron			XP_016881216.1
XM_017025728.1		Intron			XP_016881217.1
XM_017025729.1		Intron			XP_016881218.1
XM_017025730.1		Intron			XP_016881219.1
XM_017025731.1		Intron			XP_016881220.1
XM_017025732.1		Intron			XP_016881221.1
XM_017025733.1		Intron			XP_016881222.1
XM_017025734.1		Intron			XP_016881223.1
XM_017025735.1		Intron			XP_016881224.1
XM_017025736.1		Intron			XP_016881225.1
XM_017025737.1		Intron			XP_016881226.1
XM_017025738.1		Intron			XP_016881227.1
XM_017025739.1		Intron			XP_016881228.1
XM_017025740.1		Intron			XP_016881229.1
XM_017025741.1		Intron			XP_016881230.1
XM_017025742.1		Intron			XP_016881231.1

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