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TCAGCACCCCATGTGGGTGTCTCAC[A/G]GGCTTCTCAAACTCACGTCTCCTCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609149 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC29A4 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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SLC29A4 - solute carrier family 29 member 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001040661.1 | Intron | NP_001035751.1 | ||||
NM_001300847.1 | Intron | NP_001287776.1 | ||||
NM_153247.2 | Intron | NP_694979.2 | ||||
XM_005249658.4 | Intron | XP_005249715.1 | ||||
XM_006715667.3 | Intron | XP_006715730.1 | ||||
XM_006715668.2 | Intron | XP_006715731.1 | ||||
XM_011515200.2 | Intron | XP_011513502.1 | ||||
XM_011515201.2 | Intron | XP_011513503.1 |