Product Details

SNP ID
rs6800762
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:150410593 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CACGGCGGCCACCCTTCCCGTGGGC[A/T]CCGGCCAGAATGCTTCCTCGGTGGG
Phenotype
Polymorphism
A/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 2259 Missense Mutation ACC,TCC T415S NP_001290193.1
NM_014779.3 2259 Missense Mutation ACC,TCC T415S NP_055594.1
XM_011513337.2 2259 Missense Mutation ACC,TCC T415S XP_011511639.1

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