Product Details

SNP ID
rs146953990
Assay Type
Functionally Tested
NCBI dbSNP Submissions
9
Location
Chr.14:91969833 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGGGTTAATAAGAGGTACAGCTGCC[A/G]AGCGAGGAGCCAAAAACGGATTTAC
Phenotype
MIM: 604505
Polymorphism
A/G, 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 6175 Missense Mutation TCG,TTG S1926L NP_001308780.1
NM_004239.4 6175 Missense Mutation TCG,TTG S1927L NP_004230.2
XM_017021787.1 6175 Missense Mutation TCG,TTG S1692L XP_016877276.1
XM_017021788.1 6175 Missense Mutation TCG,TTG S1485L XP_016877277.1

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