Product Details

SNP ID
rs116190933
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.14:50977515 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACGGAATTCAAGAAGAATCCTGCCT[A/G]TGGTAACAGGCTGCTCACCATGGTG
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 5570 Intron NP_055978.4
NM_052978.4 5570 Intron NP_443210.1
XM_005267301.3 5570 Intron XP_005267358.1
XM_005267302.3 5570 Intron XP_005267359.1
XM_006720018.3 5570 Intron XP_006720081.1
XM_011536389.2 5570 UTR 3 XP_011534691.1
XM_017020943.1 5570 Intron XP_016876432.1
XM_017020944.1 5570 Intron XP_016876433.1
XM_017020945.1 5570 Intron XP_016876434.1
XM_017020946.1 5570 Intron XP_016876435.1
XM_017020947.1 5570 Intron XP_016876436.1
XM_017020948.1 5570 Intron XP_016876437.1
XM_017020949.1 5570 Intron XP_016876438.1
XM_017020950.1 5570 Intron XP_016876439.1

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