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TGCGGGGATAGCAGAGGTGGCTGTC[A/G]GGTGGTGGAGCGGGGGCAGGTCTGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603080 MIM: 615097 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC6A12 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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SLC6A12 - solute carrier family 6 member 12 | ||||||
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There are no transcripts associated with this gene. |
SLC6A13 - solute carrier family 6 member 13 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001190997.2 | Intron | NP_001177926.1 | ||||
NM_001243392.1 | Intron | NP_001230321.1 | ||||
NM_016615.4 | Intron | NP_057699.2 | ||||
XM_006719008.3 | Intron | XP_006719071.1 | ||||
XM_011521012.2 | Intron | XP_011519314.1 | ||||
XM_011521013.1 | Intron | XP_011519315.1 | ||||
XM_011521014.1 | Intron | XP_011519316.1 | ||||
XM_017019842.1 | Intron | XP_016875331.1 | ||||
XM_017019843.1 | Intron | XP_016875332.1 | ||||
XM_017019844.1 | Intron | XP_016875333.1 | ||||
XM_017019845.1 | Intron | XP_016875334.1 | ||||
XM_017019846.1 | Intron | XP_016875335.1 | ||||
XM_017019847.1 | Intron | XP_016875336.1 |