Product Details

SNP ID

rs829062

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:21801367 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTATCATTTATTTACATATTTTTAA[G/T]CAATGGCCAATATGGCTGGGTTTTC

Phenotype

MIM: 601439

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

ABCC9 PubMed Links

Gene Details

Gene

ABCC9

Gene Name

ATP binding cassette subfamily C member 9

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005691.3		Intron			NP_005682.2
NM_020297.3		Intron			NP_064693.2
XM_005253284.3		Intron			XP_005253341.1
XM_005253286.3		Intron			XP_005253343.1
XM_005253287.4		Intron			XP_005253344.1
XM_005253288.3		Intron			XP_005253345.1
XM_005253289.3		Intron			XP_005253346.1
XM_005253290.3		Intron			XP_005253347.1
XM_006719025.3		Intron			XP_006719088.1
XM_011520545.2		Intron			XP_011518847.1

View Full Product Details