Product Details

SNP ID
rs200087702
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:150409858 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTTTCGCGTGATCAAGCTGGACCAC[G/T]GGAGCGGAGAGCCCTATAGACGCGG
Phenotype
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
TSC22D2 PubMed Links

Gene Details

Gene
TSC22D2
Gene Name
TSC22 domain family member 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001303264.1 1524 Missense Mutation GGG,TGG G170W NP_001290193.1
NM_014779.3 1524 Missense Mutation GGG,TGG G170W NP_055594.1
XM_011513337.2 1524 Missense Mutation GGG,TGG G170W XP_011511639.1

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