Product Details

SNP ID

rs9261547

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:30187151 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GACTCTACCCCAATTACTGCACTGG[A/G]GTTCTACAAGCTTCAAGAGCATCTG

Phenotype

MIM: 600830

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

TRIM26 PubMed Links

Gene Details

Gene

TRIM26

Gene Name

tripartite motif containing 26

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001242783.1		Intron			NP_001229712.1
NM_003449.4		Intron			NP_003440.1
XM_005249374.2		Intron			XP_005249431.1
XM_005249375.2		Intron			XP_005249432.1
XM_005249376.2		Intron			XP_005249433.1
XM_005249377.2		Intron			XP_005249434.1
XM_005249378.2		Intron			XP_005249435.1
XM_006715180.2		Intron			XP_006715243.1
XM_011514859.1		Intron			XP_011513161.1
XM_017011263.1		Intron			XP_016866752.1

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