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GAGGCATCGCCCGGCTAAGCTTGGC[C/G]CTGGCAGATGGGTCGCAGGAACAGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613868 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC14A1 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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SLC14A1 - solute carrier family 14 member 1 (Kidd blood group) | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001128588.3 | 321 | Silent Mutation | GCC,GCG | A,A 41 | NP_001122060.3 | |
NM_001146036.2 | 321 | UTR 5 | NP_001139508.2 | |||
NM_001146037.1 | 321 | Silent Mutation | GCC,GCG | A,A 41 | NP_001139509.1 | |
NM_001308278.1 | 321 | Intron | NP_001295207.1 | |||
NM_001308279.1 | 321 | Intron | NP_001295208.1 | |||
NM_015865.6 | 321 | Intron | NP_056949.4 | |||
XM_005258329.1 | 321 | Silent Mutation | GCC,GCG | A,A 41 | XP_005258386.1 | |
XM_005258333.1 | 321 | Intron | XP_005258390.1 | |||
XM_006722526.3 | 321 | Intron | XP_006722589.1 | |||
XM_011526142.1 | 321 | Intron | XP_011524444.1 | |||
XM_011526144.1 | 321 | Silent Mutation | GCC,GCG | A,A 41 | XP_011524446.1 |