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CGGAGCTGCTGGTGGTGAAGGAGCG[C/T]AACGGCGTCCAGTGCCTGCTGGCGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 163970 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC6A2 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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SLC6A2 - solute carrier family 6 member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001043.3 | 708 | Silent Mutation | CGC,CGT | R,R 39 | NP_001034.1 | |
NM_001172501.1 | 708 | Silent Mutation | CGC,CGT | R,R 39 | NP_001165972.1 | |
NM_001172502.1 | 708 | Intron | NP_001165973.1 | |||
NM_001172504.1 | 708 | Silent Mutation | CGC,CGT | R,R 39 | NP_001165975.1 | |
XM_006721263.2 | 708 | Silent Mutation | CGC,CGT | R,R 39 | XP_006721326.1 | |
XM_011523295.1 | 708 | Silent Mutation | CGC,CGT | R,R 39 | XP_011521597.1 | |
XM_011523296.1 | 708 | Silent Mutation | CGC,CGT | R,R 39 | XP_011521598.1 | |
XM_011523297.2 | 708 | Silent Mutation | CGC,CGT | R,R 39 | XP_011521599.1 | |
XM_011523298.1 | 708 | Silent Mutation | CGC,CGT | R,R 39 | XP_011521600.1 | |
XM_011523299.2 | 708 | Intron | XP_011521601.1 | |||
XM_011523300.2 | 708 | Intron | XP_011521602.1 |