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CGTGGTGGTCATCTACTTTGTCTTC[A/G]TCATTGCTGTGGGGATCTGGGTAAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
15 submissions
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Phenotype: |
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Literature Links: |
SLC5A9 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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SLC5A9 - solute carrier family 5 member 9 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001011547.2 | 182 | Missense Mutation | ATC,GTC | I,V 48 | NP_001011547.2 | |
NM_001135181.1 | 182 | Missense Mutation | ATC,GTC | I,V 48 | NP_001128653.1 | |
XM_011540924.2 | 182 | Missense Mutation | ATC,GTC | I,V 48 | XP_011539226.1 | |
XM_011540925.2 | 182 | Missense Mutation | ATC,GTC | I,V 48 | XP_011539227.1 | |
XM_011540926.2 | 182 | UTR 5 | XP_011539228.1 | |||
XM_011540927.1 | 182 | Intron | XP_011539229.1 | |||
XM_011540928.1 | 182 | UTR 5 | XP_011539230.1 | |||
XM_011540929.2 | 182 | Missense Mutation | ATC,GTC | I,V 48 | XP_011539231.1 | |
XM_017000558.1 | 182 | Missense Mutation | ATC,GTC | I,V 48 | XP_016856047.1 |