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ATTGTTGAAAATCTGGTTTATAGCC[C/T]TTGATGTCTAATCTTTCATAGCGTC
Species: |
Human | ||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611039 | ||||||||||||||||||||||||||||||||
Literature Links: |
SLC2A14 PubMed Links | ||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global - Not Available | Caucasian - Not Available | CEPH (CEU)
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EAS - Not Available | African American - Not Available | YRI (Yoruba)
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SAS - Not Available | Chinese - Not Available | JPT (Japanese)
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AFR - Not Available | Japanese - Not Available | CHB (Han Chinese)
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EUR - Not Available | |||||
AMR - Not Available |
SLC2A14 - solute carrier family 2 member 14 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001286233.1 | Intron | NP_001273162.1 | ||||
NM_001286234.1 | Intron | NP_001273163.1 | ||||
NM_001286235.1 | Intron | NP_001273164.1 | ||||
NM_001286236.1 | Intron | NP_001273165.1 | ||||
NM_001286237.1 | Intron | NP_001273166.1 | ||||
NM_153449.3 | Intron | NP_703150.1 | ||||
XM_005253315.3 | Intron | XP_005253372.1 | ||||
XM_005253317.4 | Intron | XP_005253374.1 | ||||
XM_011520562.1 | Intron | XP_011518864.1 | ||||
XM_011520563.2 | Intron | XP_011518865.1 | ||||
XM_011520564.2 | Intron | XP_011518866.1 | ||||
XM_011520565.2 | Intron | XP_011518867.1 | ||||
XM_017018841.1 | Intron | XP_016874330.1 | ||||
XM_017018842.1 | Intron | XP_016874331.1 | ||||
XM_017018843.1 | Intron | XP_016874332.1 | ||||
XM_017018844.1 | Intron | XP_016874333.1 | ||||
XM_017018845.1 | Intron | XP_016874334.1 | ||||
XM_017018846.1 | Intron | XP_016874335.1 | ||||
XM_017018847.1 | Intron | XP_016874336.1 |