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Search Thermo Fisher Scientific
TGCTGAACTGAGCAAGGACGCCCAG[C/G]CGTCAGCCGCCCCTGCAGCACCCTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602193 | ||||||||||||||||||||
Literature Links: |
SLC29A1 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 |
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 | 480 | Missense Mutation | CCG,GCG | P,A 62 | NP_001071643.1 | |
NM_001078177.1 | 480 | Missense Mutation | CCG,GCG | P,A 62 | NP_001071645.1 | |
NM_001304462.1 | 480 | Missense Mutation | CCG,GCG | P,A 141 | NP_001291391.1 | |
NM_001304463.1 | 480 | Missense Mutation | CCG,GCG | P,A 104 | NP_001291392.1 | |
NM_001304465.1 | 480 | Missense Mutation | CCG,GCG | P,A 88 | NP_001291394.1 | |
NM_001304466.1 | 480 | Missense Mutation | CCG,GCG | P,A 87 | NP_001291395.1 | |
XM_005248876.4 | 480 | Missense Mutation | CCG,GCG | P,A 105 | XP_005248933.1 | |
XM_005248878.3 | 480 | Missense Mutation | CCG,GCG | P,A 62 | XP_005248935.1 | |
XM_005248879.3 | 480 | Missense Mutation | CCG,GCG | P,A 62 | XP_005248936.1 | |
XM_005248880.3 | 480 | Missense Mutation | CCG,GCG | P,A 62 | XP_005248937.1 | |
XM_005248881.3 | 480 | Missense Mutation | CCG,GCG | P,A 62 | XP_005248938.1 | |
XM_005248882.3 | 480 | Missense Mutation | CCG,GCG | P,A 62 | XP_005248939.1 | |
XM_011514341.2 | 480 | Missense Mutation | CCG,GCG | P,A 142 | XP_011512643.1 |