Product Details

SNP ID
rs201674442
Assay Type
Functionally tested
NCBI dbSNP Submissions
3
Location
Chr.1:27879955 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCCTCGAACTCTGCTCCAGGTCCTA[C/G]AGGATCCAGCCCTGAAAGACCTCGT
Phenotype
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
THEMIS2 PubMed Links

Gene Details

Gene
THEMIS2
Gene Name
thymocyte selection associated family member 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001039477.2 576 Intron NP_001034566.1
NM_001105556.2 576 Missense Mutation CAG,GAG Q183E NP_001099026.1
NM_001286113.1 576 Missense Mutation CAG,GAG Q183E NP_001273042.1
NM_001286115.1 576 Missense Mutation CAG,GAG Q183E NP_001273044.1
NM_004848.3 576 Missense Mutation CAG,GAG Q183E NP_004839.2
XM_005246041.3 576 Intron XP_005246098.1
XM_006711050.1 576 Missense Mutation CAG,GAG Q183E XP_006711113.1
XM_011542445.2 576 Missense Mutation CAG,GAG Q136E XP_011540747.1

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