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TCATGAGTATAACCATGATCAGGCC[G/T]ACAGCATTCCATCAGTGTCTTTGCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604506 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TRIP12 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
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
|
TRIP12 - thyroid hormone receptor interactor 12 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001284214.1 | 5918 | Silent Mutation | AGG,CGG | R,R 1932 | NP_001271143.1 | |
NM_001284215.1 | 5918 | Silent Mutation | AGG,CGG | R,R 1917 | NP_001271144.1 | |
NM_001284216.1 | 5918 | Silent Mutation | AGG,CGG | R,R 1614 | NP_001271145.1 | |
NM_004238.2 | 5918 | Silent Mutation | AGG,CGG | R,R 1884 | NP_004229.1 | |
XM_005246954.4 | 5918 | Silent Mutation | AGG,CGG | R,R 1960 | XP_005247011.1 | |
XM_005246955.4 | 5918 | Silent Mutation | AGG,CGG | R,R 1960 | XP_005247012.1 | |
XM_005246956.4 | 5918 | Silent Mutation | AGG,CGG | R,R 1959 | XP_005247013.1 | |
XM_005246957.4 | 5918 | Silent Mutation | AGG,CGG | R,R 1955 | XP_005247014.1 | |
XM_005246958.4 | 5918 | Silent Mutation | AGG,CGG | R,R 1933 | XP_005247015.1 | |
XM_005246960.4 | 5918 | Silent Mutation | AGG,CGG | R,R 1931 | XP_005247017.1 | |
XM_005246961.3 | 5918 | Silent Mutation | AGG,CGG | R,R 1918 | XP_005247018.1 | |
XM_005246962.4 | 5918 | Silent Mutation | AGG,CGG | R,R 1917 | XP_005247019.1 | |
XM_006712852.3 | 5918 | Silent Mutation | AGG,CGG | R,R 1918 | XP_006712915.1 | |
XM_011512180.2 | 5918 | Silent Mutation | AGG,CGG | R,R 1960 | XP_011510482.1 | |
XM_011512181.2 | 5918 | Silent Mutation | AGG,CGG | R,R 1960 | XP_011510483.1 | |
XM_011512183.2 | 5918 | Silent Mutation | AGG,CGG | R,R 1918 | XP_011510485.1 | |
XM_017005272.1 | 5918 | Silent Mutation | AGG,CGG | R,R 1960 | XP_016860761.1 | |
XM_017005273.1 | 5918 | Silent Mutation | AGG,CGG | R,R 1960 | XP_016860762.1 | |
XM_017005274.1 | 5918 | Silent Mutation | AGG,CGG | R,R 1960 | XP_016860763.1 | |
XM_017005275.1 | 5918 | Silent Mutation | AGG,CGG | R,R 1959 | XP_016860764.1 | |
XM_017005276.1 | 5918 | Silent Mutation | AGG,CGG | R,R 1959 | XP_016860765.1 | |
XM_017005277.1 | 5918 | Silent Mutation | AGG,CGG | R,R 1959 | XP_016860766.1 | |
XM_017005278.1 | 5918 | Silent Mutation | AGG,CGG | R,R 1959 | XP_016860767.1 | |
XM_017005279.1 | 5918 | Silent Mutation | AGG,CGG | R,R 1954 | XP_016860768.1 | |
XM_017005280.1 | 5918 | Silent Mutation | AGG,CGG | R,R 1954 | XP_016860769.1 | |
XM_017005281.1 | 5918 | Silent Mutation | AGG,CGG | R,R 1932 | XP_016860770.1 | |
XM_017005282.1 | 5918 | Silent Mutation | AGG,CGG | R,R 1931 | XP_016860771.1 | |
XM_017005283.1 | 5918 | Silent Mutation | AGG,CGG | R,R 1927 | XP_016860772.1 | |
XM_017005284.1 | 5918 | Silent Mutation | AGG,CGG | R,R 1925 | XP_016860773.1 | |
XM_017005285.1 | 5918 | Silent Mutation | AGG,CGG | R,R 1918 | XP_016860774.1 | |
XM_017005286.1 | 5918 | Silent Mutation | AGG,CGG | R,R 1917 | XP_016860775.1 | |
XM_017005287.1 | 5918 | Silent Mutation | AGG,CGG | R,R 1912 | XP_016860776.1 | |
XM_017005288.1 | 5918 | Silent Mutation | AGG,CGG | R,R 1912 | XP_016860777.1 | |
XM_017005289.1 | 5918 | Silent Mutation | AGG,CGG | R,R 1904 | XP_016860778.1 | |
XM_017005290.1 | 5918 | Silent Mutation | AGG,CGG | R,R 1903 | XP_016860779.1 | |
XM_017005291.1 | 5918 | Silent Mutation | AGG,CGG | R,R 1889 | XP_016860780.1 | |
XM_017005292.1 | 5918 | Silent Mutation | AGG,CGG | R,R 1885 | XP_016860781.1 | |
XM_017005293.1 | 5918 | Silent Mutation | AGG,CGG | R,R 1890 | XP_016860782.1 |