Product Details

SNP ID
rs116220382
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.2:229771365 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTATTTAACATTCTTCCTTGCTCA[A/G]GCAATTTCCTTGTCTTTCCCAAACA
Phenotype
MIM: 604506
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
TRIP12 PubMed Links

Gene Details

Gene
TRIP12
Gene Name
thyroid hormone receptor interactor 12
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001284214.1 Intron NP_001271143.1
NM_001284215.1 Intron NP_001271144.1
NM_001284216.1 Intron NP_001271145.1
NM_004238.2 Intron NP_004229.1
XM_005246954.4 Intron XP_005247011.1
XM_005246955.4 Intron XP_005247012.1
XM_005246956.4 Intron XP_005247013.1
XM_005246957.4 Intron XP_005247014.1
XM_005246958.4 Intron XP_005247015.1
XM_005246960.4 Intron XP_005247017.1
XM_005246961.3 Intron XP_005247018.1
XM_005246962.4 Intron XP_005247019.1
XM_006712852.3 Intron XP_006712915.1
XM_011512180.2 Intron XP_011510482.1
XM_011512181.2 Intron XP_011510483.1
XM_011512183.2 Intron XP_011510485.1
XM_017005272.1 Intron XP_016860761.1
XM_017005273.1 Intron XP_016860762.1
XM_017005274.1 Intron XP_016860763.1
XM_017005275.1 Intron XP_016860764.1
XM_017005276.1 Intron XP_016860765.1
XM_017005277.1 Intron XP_016860766.1
XM_017005278.1 Intron XP_016860767.1
XM_017005279.1 Intron XP_016860768.1
XM_017005280.1 Intron XP_016860769.1
XM_017005281.1 Intron XP_016860770.1
XM_017005282.1 Intron XP_016860771.1
XM_017005283.1 Intron XP_016860772.1
XM_017005284.1 Intron XP_016860773.1
XM_017005285.1 Intron XP_016860774.1
XM_017005286.1 Intron XP_016860775.1
XM_017005287.1 Intron XP_016860776.1
XM_017005288.1 Intron XP_016860777.1
XM_017005289.1 Intron XP_016860778.1
XM_017005290.1 Intron XP_016860779.1
XM_017005291.1 Intron XP_016860780.1
XM_017005292.1 Intron XP_016860781.1
XM_017005293.1 Intron XP_016860782.1

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