Product Details

SNP ID
rs17855956
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:28981494 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGTGACACCGGGTCTAGGAGTGGTG[C/G]CCGTTCTGCTGCTGTTCCTGGTAGT
Phenotype
MIM: 602354 MIM: 612583
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
LAT PubMed Links

Gene Details

Gene
LAT
Gene Name
linker for activation of T-cells
There are no transcripts associated with this gene.

Gene
SPNS1
Gene Name
sphingolipid transporter 1 (putative)
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001142448.1 1065 Missense Mutation CCC,GCC P230A NP_001135920.1
NM_001142449.1 1065 Missense Mutation CCC,GCC P208A NP_001135921.1
NM_001142450.1 1065 Missense Mutation CCC,GCC P157A NP_001135922.1
NM_001142451.1 1065 Missense Mutation CCC,GCC P230A NP_001135923.1
NM_032038.2 1065 Missense Mutation CCC,GCC P230A NP_114427.1
XM_006721096.3 1065 Missense Mutation CCC,GCC P275A XP_006721159.1
XM_017023757.1 1065 Missense Mutation CCC,GCC P280A XP_016879246.1
XM_017023758.1 1065 Missense Mutation CCC,GCC P280A XP_016879247.1
XM_017023759.1 1065 Missense Mutation CCC,GCC P275A XP_016879248.1

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