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AGAAAAAGAAGGTGTCCTGCTTTTC[C/T]AACATCAAGATCTTCCTGGTGTCCG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612435 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLCO3A1 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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SLCO3A1 - solute carrier organic anion transporter family member 3A1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145044.1 | 312 | Silent Mutation | TCC,TCT | S,S 37 | NP_001138516.1 | |
NM_013272.3 | 312 | Silent Mutation | TCC,TCT | S,S 37 | NP_037404.2 | |
XM_005254889.1 | 312 | Silent Mutation | TCC,TCT | S,S 37 | XP_005254946.1 | |
XM_005254891.2 | 312 | Intron | XP_005254948.1 | |||
XM_011521456.2 | 312 | Intron | XP_011519758.1 |