Product Details

SNP ID

rs4380112

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.18:79071142 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGAGATTAGGTGTTGGTATAGTTTT[C/T]ACAGTGCTTGCTCTGGGTATTACAA

Phenotype

MIM: 614446

Polymorphism

C/T, Transition 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		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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