Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGCCCTCTGTCTCCCAGGTGACACC[A/G]GGTCTAGGAGTGGTGGCCGTTCTGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 602354 MIM: 612583 | ||||||||||||||||||||
Literature Links: |
LAT PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
LAT - linker for activation of T-cells | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
SPNS1 - sphingolipid transporter 1 (putative) | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001142448.1 | 1049 | Silent Mutation | CCA,CCG | P,P 224 | NP_001135920.1 | |
NM_001142449.1 | 1049 | Silent Mutation | CCA,CCG | P,P 202 | NP_001135921.1 | |
NM_001142450.1 | 1049 | Silent Mutation | CCA,CCG | P,P 151 | NP_001135922.1 | |
NM_001142451.1 | 1049 | Silent Mutation | CCA,CCG | P,P 224 | NP_001135923.1 | |
NM_032038.2 | 1049 | Silent Mutation | CCA,CCG | P,P 224 | NP_114427.1 | |
XM_006721096.3 | 1049 | Silent Mutation | CCA,CCG | P,P 269 | XP_006721159.1 | |
XM_017023757.1 | 1049 | Silent Mutation | CCA,CCG | P,P 274 | XP_016879246.1 | |
XM_017023758.1 | 1049 | Silent Mutation | CCA,CCG | P,P 274 | XP_016879247.1 | |
XM_017023759.1 | 1049 | Silent Mutation | CCA,CCG | P,P 269 | XP_016879248.1 |