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AACATCTAGGCTAGCAGGCATTAAA[C/T]GGAATTCAAGAAGAATCCTGCCTAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606555 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TRIM9 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
|
TRIM9 - tripartite motif containing 9 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015163.5 | 5594 | Intron | NP_055978.4 | |||
NM_052978.4 | 5594 | Intron | NP_443210.1 | |||
XM_005267301.3 | 5594 | Intron | XP_005267358.1 | |||
XM_005267302.3 | 5594 | Intron | XP_005267359.1 | |||
XM_006720018.3 | 5594 | Intron | XP_006720081.1 | |||
XM_011536389.2 | 5594 | UTR 3 | XP_011534691.1 | |||
XM_017020943.1 | 5594 | Intron | XP_016876432.1 | |||
XM_017020944.1 | 5594 | Intron | XP_016876433.1 | |||
XM_017020945.1 | 5594 | Intron | XP_016876434.1 | |||
XM_017020946.1 | 5594 | Intron | XP_016876435.1 | |||
XM_017020947.1 | 5594 | Intron | XP_016876436.1 | |||
XM_017020948.1 | 5594 | Intron | XP_016876437.1 | |||
XM_017020949.1 | 5594 | Intron | XP_016876438.1 | |||
XM_017020950.1 | 5594 | Intron | XP_016876439.1 |