Product Details

SNP ID

rs117769984

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:49859724 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCAGTCTGAAAGCAACACAGTACA[C/T]GCTTTAAATTTTAAAAGTATACCTT

Phenotype

MIM: 609123

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

ATP8B4 PubMed Links

Gene Details

Gene

ATP8B4

Gene Name

ATPase phospholipid transporting 8B4 (putative)

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_024837.3	4402	UTR 3			NP_079113.2
XM_011522046.2	4402	UTR 3			XP_011520348.1
XM_011522047.2	4402	UTR 3			XP_011520349.1
XM_011522048.1	4402	UTR 3			XP_011520350.1
XM_011522049.2	4402	UTR 3			XP_011520351.1
XM_011522051.2	4402	UTR 3			XP_011520353.1
XM_011522052.2	4402	UTR 3			XP_011520354.1
XM_011522053.1	4402	UTR 3			XP_011520355.1
XM_011522056.2	4402	UTR 3			XP_011520358.2
XM_011522058.2	4402	UTR 3			XP_011520360.1
XM_011522059.1	4402	UTR 3			XP_011520361.1
XM_011522060.1	4402	UTR 3			XP_011520362.1
XM_011522061.1	4402	UTR 3			XP_011520363.1
XM_011522062.1	4402	UTR 3			XP_011520364.1
XM_011522063.1	4402	UTR 3			XP_011520365.1
XM_011522064.1	4402	UTR 3			XP_011520366.1
XM_011522069.2	4402	UTR 3			XP_011520371.1
XM_011522070.1	4402	UTR 3			XP_011520372.1
XM_017022587.1	4402	UTR 3			XP_016878076.1
XM_017022588.1	4402	UTR 3			XP_016878077.1
XM_017022589.1	4402	UTR 3			XP_016878078.1
XM_017022590.1	4402	UTR 3			XP_016878079.1
XM_017022591.1	4402	UTR 3			XP_016878080.1
XM_017022592.1	4402	UTR 3			XP_016878081.1
XM_017022593.1	4402	Intron			XP_016878082.1
XM_017022594.1	4402	UTR 3			XP_016878083.1
XM_017022595.1	4402	UTR 3			XP_016878084.1
XM_017022596.1	4402	UTR 3			XP_016878085.1
XM_017022597.1	4402	Intron			XP_016878086.1
XM_017022598.1	4402	Intron			XP_016878087.1
XM_017022599.1	4402	Intron			XP_016878088.1

View Full Product Details