Product Details

SNP ID

rs6453465

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:79615370 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GAGGAAAAACAGCATATTTTTTATA[A/G]GTATAAACAAAAGTATCTAGGCTTT

Phenotype

MIM: 614121

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

PAPD4 PubMed Links

Gene Details

Gene

PAPD4

Gene Name

PAP associated domain containing 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001114393.1		Intron			NP_001107865.1
NM_001114394.1		Intron			NP_001107866.1
NM_001297744.1		Intron			NP_001284673.1
NM_001297745.1		Intron			NP_001284674.1
NM_173797.3		Intron			NP_776158.2
XM_011543219.2		Intron			XP_011541521.1
XM_011543220.2		Intron			XP_011541522.1
XM_011543221.2		Intron			XP_011541523.1
XM_011543222.2		Intron			XP_011541524.1
XM_011543223.2		Intron			XP_011541525.1
XM_011543224.2		Intron			XP_011541526.1
XM_011543225.2		Intron			XP_011541527.1
XM_011543226.2		Intron			XP_011541528.1
XM_011543227.2		Intron			XP_011541529.1
XM_011543228.2		Intron			XP_011541530.1
XM_011543229.2		Intron			XP_011541531.1
XM_011543230.2		Intron			XP_011541532.1
XM_011543231.2		Intron			XP_011541533.1
XM_011543232.2		Intron			XP_011541534.1
XM_011543233.2		Intron			XP_011541535.1
XM_017009151.1		Intron			XP_016864640.1
XM_017009152.1		Intron			XP_016864641.1
XM_017009153.1		Intron			XP_016864642.1
XM_017009154.1		Intron			XP_016864643.1
XM_017009155.1		Intron			XP_016864644.1
XM_017009156.1		Intron			XP_016864645.1
XM_017009157.1		Intron			XP_016864646.1
XM_017009158.1		Intron			XP_016864647.1
XM_017009159.1		Intron			XP_016864648.1
XM_017009160.1		Intron			XP_016864649.1
XM_017009161.1		Intron			XP_016864650.1
XM_017009162.1		Intron			XP_016864651.1

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