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CTCACCCTCTCTTTGAAGCCAACAG[C/T]GTGGCGAGCTACGAGAACGAGGGTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602354 MIM: 612583 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LAT PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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LAT - linker for activation of T-cells | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001014987.1 | 670 | Silent Mutation | AGC,AGT | S,S 106 | NP_001014987.1 | |
NM_001014988.1 | 670 | Silent Mutation | AGC,AGT | S,S 105 | NP_001014988.1 | |
NM_001014989.1 | 670 | Silent Mutation | AGC,AGT | S,S 142 | NP_001014989.2 | |
NM_014387.3 | 670 | Silent Mutation | AGC,AGT | S,S 106 | NP_055202.1 |
SPNS1 - sphingolipid transporter 1 (putative) | ||||||
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There are no transcripts associated with this gene. |