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TATGAACGTCTTGGCCTTGGTCTCC[A/G]GGACAATCAAGAAGATGTAGATGGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
4 submissions
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Phenotype: |
MIM: 138230 | ||||||||||||||||||||
Literature Links: |
SLC2A5 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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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 |
SLC2A5 - solute carrier family 2 member 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001135585.1 | 1603 | Intron | NP_001129057.1 | |||
NM_003039.2 | 1603 | Missense Mutation | CCG,CTG | P,L 461 | NP_003030.1 | |
XM_005263491.3 | 1603 | Missense Mutation | CCG,CTG | P,L 461 | XP_005263548.1 | |
XM_017002133.1 | 1603 | Missense Mutation | CCG,CTG | P,L 461 | XP_016857622.1 | |
XM_017002134.1 | 1603 | Missense Mutation | CCG,CTG | P,L 461 | XP_016857623.1 | |
XM_017002135.1 | 1603 | Missense Mutation | CCG,CTG | P,L 461 | XP_016857624.1 | |
XM_017002136.1 | 1603 | Missense Mutation | CCG,CTG | P,L 461 | XP_016857625.1 | |
XM_017002137.1 | 1603 | Missense Mutation | CCG,CTG | P,L 461 | XP_016857626.1 | |
XM_017002138.1 | 1603 | Missense Mutation | CCG,CTG | P,L 461 | XP_016857627.1 | |
XM_017002139.1 | 1603 | Missense Mutation | CCG,CTG | P,L 461 | XP_016857628.1 | |
XM_017002140.1 | 1603 | Missense Mutation | CCG,CTG | P,L 461 | XP_016857629.1 | |
XM_017002141.1 | 1603 | Missense Mutation | CCG,CTG | P,L 461 | XP_016857630.1 | |
XM_017002142.1 | 1603 | Missense Mutation | CCG,CTG | P,L 402 | XP_016857631.1 |