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GGGTGTGCTTCTGCTTCTTTGCTTG[C/G]AAGGCTTCTCAGAATGGGGCCCCAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602193 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
LOC101929726 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)
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SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | ||||||
AFR
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Japanese - Not Available | JPT (Japanese)
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EUR
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AMR
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LOC101929726 - uncharacterized LOC101929726 | ||||||
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There are no transcripts associated with this gene. |
SLC29A1 - solute carrier family 29 member 1 (Augustine blood group) | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001078175.2 | Intron | NP_001071643.1 | ||||
NM_001078177.1 | Intron | NP_001071645.1 | ||||
NM_001304462.1 | Intron | NP_001291391.1 | ||||
NM_001304463.1 | Intron | NP_001291392.1 | ||||
NM_001304465.1 | Intron | NP_001291394.1 | ||||
NM_001304466.1 | Intron | NP_001291395.1 | ||||
XM_005248876.4 | Intron | XP_005248933.1 | ||||
XM_005248878.3 | Intron | XP_005248935.1 | ||||
XM_005248879.3 | Intron | XP_005248936.1 | ||||
XM_005248880.3 | Intron | XP_005248937.1 | ||||
XM_005248881.3 | Intron | XP_005248938.1 | ||||
XM_005248882.3 | Intron | XP_005248939.1 | ||||
XM_011514341.2 | Intron | XP_011512643.1 |
Set Membership: |
HapMap |