Product Details

SNP ID

rs12879906

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.14:50975912 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

CTATCAGTCATAGTAATGACATACA[A/G]TCCCATGTTTTTCCAAACATTGTTT

Phenotype

MIM: 606555

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

TRIM9 PubMed Links

Gene Details

Gene

TRIM9

Gene Name

tripartite motif containing 9

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015163.5	4894	UTR 3			NP_055978.4
NM_052978.4	4894	Intron			NP_443210.1
XM_005267301.3	4894	UTR 3			XP_005267358.1
XM_005267302.3	4894	UTR 3			XP_005267359.1
XM_006720018.3	4894	UTR 3			XP_006720081.1
XM_011536389.2	4894	Intron			XP_011534691.1
XM_017020943.1	4894	UTR 3			XP_016876432.1
XM_017020944.1	4894	UTR 3			XP_016876433.1
XM_017020945.1	4894	UTR 3			XP_016876434.1
XM_017020946.1	4894	UTR 3			XP_016876435.1
XM_017020947.1	4894	UTR 3			XP_016876436.1
XM_017020948.1	4894	UTR 3			XP_016876437.1
XM_017020949.1	4894	UTR 3			XP_016876438.1
XM_017020950.1	4894	UTR 3			XP_016876439.1

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