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GGTCCTGCTGGGTTCCGCTGGGGCA[A/G]GTCCTCGGCTGGGCACATGAGCTGA
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 |
---|---|---|
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 |
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 | 1878 | Silent Mutation | CTG,TTG | L,L 482 | NP_001177926.1 | |
NM_001243392.1 | 1878 | Intron | NP_001230321.1 | |||
NM_016615.4 | 1878 | Silent Mutation | CTG,TTG | L,L 574 | NP_057699.2 | |
XM_006719008.3 | 1878 | Silent Mutation | CTG,TTG | L,L 331 | XP_006719071.1 | |
XM_011521012.2 | 1878 | Silent Mutation | CTG,TTG | L,L 455 | XP_011519314.1 | |
XM_011521013.1 | 1878 | Silent Mutation | CTG,TTG | L,L 412 | XP_011519315.1 | |
XM_011521014.1 | 1878 | Silent Mutation | CTG,TTG | L,L 412 | XP_011519316.1 | |
XM_017019842.1 | 1878 | Silent Mutation | CTG,TTG | L,L 417 | XP_016875331.1 | |
XM_017019843.1 | 1878 | Silent Mutation | CTG,TTG | L,L 414 | XP_016875332.1 | |
XM_017019844.1 | 1878 | Intron | XP_016875333.1 | |||
XM_017019845.1 | 1878 | Silent Mutation | CTG,TTG | L,L 331 | XP_016875334.1 | |
XM_017019846.1 | 1878 | Intron | XP_016875335.1 | |||
XM_017019847.1 | 1878 | Intron | XP_016875336.1 |