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Search Thermo Fisher Scientific
GCTGCGCACTGGATCCCTTTTTGCA[A/G]GCCAGTCTCTTCGTGGAATTCTCCC
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 |
---|---|---|
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 |
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 | 2970 | UTR 3 | NP_001139480.1 | |||
NM_001146009.1 | 2970 | Silent Mutation | CTG,TTG | L,L 755 | NP_001139481.1 | |
NM_030958.2 | 2970 | Silent Mutation | CTG,TTG | L,L 810 | NP_112220.2 | |
XM_005251313.2 | 2970 | Silent Mutation | CTG,TTG | L,L 755 | XP_005251370.1 | |
XM_017013883.1 | 2970 | UTR 3 | XP_016869372.1 | |||
XM_017013884.1 | 2970 | Intron | XP_016869373.1 | |||
XM_017013885.1 | 2970 | Silent Mutation | CTG,TTG | L,L 506 | XP_016869374.1 | |
XM_017013886.1 | 2970 | Intron | XP_016869375.1 |