Product Details

SNP ID
rs113605039
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:91969713 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTCTTTCAGCACAACCCCAGCACTG[C/T]TGTCAGGTAACGCTGGCAAAGGTGT
Phenotype
MIM: 604505
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
TRIP11 PubMed Links

Gene Details

Gene
TRIP11
Gene Name
thyroid hormone receptor interactor 11
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001321851.1 6295 Missense Mutation AAC,AGC N1966S NP_001308780.1
NM_004239.4 6295 Missense Mutation AAC,AGC N1967S NP_004230.2
XM_017021787.1 6295 Missense Mutation AAC,AGC N1732S XP_016877276.1
XM_017021788.1 6295 Missense Mutation AAC,AGC N1525S XP_016877277.1

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