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GCCATGCTGGTCAACAATGTCCTGG[C/T]GGTGCTGGGGGGCAGCCTCATGGGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 138190 MIM: 611447 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC2A4 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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SLC2A4 - solute carrier family 2 member 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001042.2 | 556 | Missense Mutation | GCG,GTG | A,V 119 | NP_001033.1 |
YBX2 - Y-box binding protein 2 | ||||||
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There are no transcripts associated with this gene. |