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GGGGCTCTCTTCCAGCCCCGGGTCC[G/T]CAGAGGAACTTATTGCTTCTGGGAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613543 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLCO5A1 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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SLCO5A1 - solute carrier organic anion transporter family member 5A1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001146008.1 | 3040 | UTR 3 | NP_001139480.1 | |||
NM_001146009.1 | 3040 | Missense Mutation | GAG,GCG | E,A 778 | NP_001139481.1 | |
NM_030958.2 | 3040 | Missense Mutation | GAG,GCG | E,A 833 | NP_112220.2 | |
XM_005251313.2 | 3040 | Missense Mutation | GAG,GCG | E,A 778 | XP_005251370.1 | |
XM_017013883.1 | 3040 | UTR 3 | XP_016869372.1 | |||
XM_017013884.1 | 3040 | Intron | XP_016869373.1 | |||
XM_017013885.1 | 3040 | Missense Mutation | GAG,GCG | E,A 529 | XP_016869374.1 | |
XM_017013886.1 | 3040 | Intron | XP_016869375.1 |