Product Details

SNP ID

rs116790577

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.18:79069437 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGGCGGACCAGATCCCGCTTTACCC[G/T]GTGCGTAGCGCAGCGGCGGCCGCAG

Phenotype

MIM: 614446

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

ATP9B PubMed Links

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	163	Silent Mutation	CCG,CCT	P9P	NP_001293014.1
NM_198531.4	163	Silent Mutation	CCG,CCT	P9P	NP_940933.3
XM_011525963.2	163	UTR 5			XP_011524265.1
XM_011525964.2	163	Silent Mutation	CCG,CCT	P9P	XP_011524266.1
XM_011525965.2	163	UTR 5			XP_011524267.1
XM_011525966.2	163	Intron			XP_011524268.1
XM_011525971.2	163	Intron			XP_011524273.2
XM_011525972.2	163	Intron			XP_011524274.1
XM_011525973.2	163	Intron			XP_011524275.1
XM_011525974.2	163	Intron			XP_011524276.1
XM_017025726.1	163	UTR 5			XP_016881215.1
XM_017025727.1	163	UTR 5			XP_016881216.1
XM_017025728.1	163	UTR 5			XP_016881217.1
XM_017025729.1	163	UTR 5			XP_016881218.1
XM_017025730.1	163	UTR 5			XP_016881219.1
XM_017025731.1	163	UTR 5			XP_016881220.1
XM_017025732.1	163	UTR 5			XP_016881221.1
XM_017025733.1	163	UTR 5			XP_016881222.1
XM_017025734.1	163	UTR 5			XP_016881223.1
XM_017025735.1	163	UTR 5			XP_016881224.1
XM_017025736.1	163	UTR 5			XP_016881225.1
XM_017025737.1	163	UTR 5			XP_016881226.1
XM_017025738.1	163	Intron			XP_016881227.1
XM_017025739.1	163	Intron			XP_016881228.1
XM_017025740.1	163	Intron			XP_016881229.1
XM_017025741.1	163	Intron			XP_016881230.1
XM_017025742.1	163	UTR 5			XP_016881231.1

View Full Product Details