Product Details

SNP ID
rs112805250
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.X:107714760 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATTCTTCACCAGATCCTGCCAATGA[C/G]GGAATCATAACAAAGCCATTCCTTA
Phenotype
MIM: 300506
Polymorphism
C/G, Transversion Substitution
Allele Nomenclature
Literature Links
TSC22D3 PubMed Links

Gene Details

Gene
TSC22D3
Gene Name
TSC22 domain family member 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001015881.1 Intron NP_001015881.1
NM_001318468.1 Intron NP_001305397.1
NM_001318470.1 Intron NP_001305399.1
NM_004089.3 Intron NP_004080.2
NM_198057.2 Intron NP_932174.1
XM_005262099.1 Intron XP_005262156.1
XM_005262100.1 Intron XP_005262157.1
XM_005262102.1 Intron XP_005262159.1
XM_005262103.3 Intron XP_005262160.1
XM_011530884.1 Intron XP_011529186.1
XM_017029335.1 Intron XP_016884824.1

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