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AGTTGTTCTGCAAAACTTCAGTGCA[A/G]CCTGTTGGAAGGCCTTCTTTTAAAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 613389 | ||||||||||||||||||||
Literature Links: |
SLCO1C1 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 |
SLCO1C1 - solute carrier organic anion transporter family member 1C1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145944.1 | 198 | Intron | NP_001139416.1 | |||
NM_001145945.1 | 198 | Silent Mutation | CAA,CAG | Q,Q 18 | NP_001139417.1 | |
NM_001145946.1 | 198 | Silent Mutation | CAA,CAG | Q,Q 18 | NP_001139418.1 | |
NM_017435.4 | 198 | Silent Mutation | CAA,CAG | Q,Q 18 | NP_059131.1 | |
XM_005253394.2 | 198 | Silent Mutation | CAA,CAG | Q,Q 18 | XP_005253451.1 | |
XM_005253396.2 | 198 | Intron | XP_005253453.1 | |||
XM_011520703.2 | 198 | Silent Mutation | CAA,CAG | Q,Q 18 | XP_011519005.1 | |
XM_011520704.2 | 198 | Silent Mutation | CAA,CAG | Q,Q 18 | XP_011519006.1 | |
XM_011520709.2 | 198 | Intron | XP_011519011.1 | |||
XM_011520711.2 | 198 | Intron | XP_011519013.1 | |||
XM_017019484.1 | 198 | UTR 5 | XP_016874973.1 | |||
XM_017019485.1 | 198 | UTR 5 | XP_016874974.1 | |||
XM_017019486.1 | 198 | UTR 5 | XP_016874975.1 | |||
XM_017019487.1 | 198 | Intron | XP_016874976.1 | |||
XM_017019488.1 | 198 | UTR 5 | XP_016874977.1 | |||
XM_017019489.1 | 198 | UTR 5 | XP_016874978.1 | |||
XM_017019490.1 | 198 | UTR 5 | XP_016874979.1 |