Product Details

SNP ID
rs139864999
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:28985738 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCTCCTACGACAGCACATCCTCAGA[C/T]AGGTGAGTCCGCCCCAGCCGCCCTG
Phenotype
MIM: 602354 MIM: 612583
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
LAT PubMed Links

Gene Details

Gene
LAT
Gene Name
linker for activation of T-cells
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001014987.1 478 Silent Mutation GAC,GAT D42D NP_001014987.1
NM_001014988.1 478 Silent Mutation GAC,GAT D42D NP_001014988.1
NM_001014989.1 478 Silent Mutation GAC,GAT D78D NP_001014989.2
NM_014387.3 478 Silent Mutation GAC,GAT D42D NP_055202.1
Gene
SPNS1
Gene Name
sphingolipid transporter 1 (putative)
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001142448.1 478 Intron NP_001135920.1
NM_001142449.1 478 Intron NP_001135921.1
NM_001142450.1 478 Intron NP_001135922.1
NM_001142451.1 478 Intron NP_001135923.1
NM_032038.2 478 Intron NP_114427.1
XM_006721096.3 478 Intron XP_006721159.1
XM_017023757.1 478 Intron XP_016879246.1
XM_017023758.1 478 Intron XP_016879247.1
XM_017023759.1 478 Intron XP_016879248.1

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