Product Details

SNP ID

rs2696923

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:49032049 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTGAAGATCGATTTCTGTAAAGGAT[A/G]CATAAAATTCCTGTGGGTCTATTTT

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

TRIM49B PubMed Links

Gene Details

Gene

TRIM49B

Gene Name

tripartite motif containing 49B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001206626.1		Intron			NP_001193555.1
XM_017017561.1		Intron			XP_016873050.1

View Full Product Details