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TAGCCGTGAATAAAGACCACCACAG[C/T]CAGGAGGAGGATGGCGTTGATGTTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
SLC5A4 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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SLC5A4 - solute carrier family 5 member 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_014227.2 | 1827 | Missense Mutation | ACT,GCT | T,A 649 | NP_055042.1 | |
XM_006724308.3 | 1827 | Missense Mutation | ACT,GCT | T,A 603 | XP_006724371.1 | |
XM_011530342.2 | 1827 | Missense Mutation | ACT,GCT | T,A 603 | XP_011528644.1 | |
XM_011530343.2 | 1827 | Missense Mutation | ACT,GCT | T,A 603 | XP_011528645.1 | |
XM_011530344.2 | 1827 | Missense Mutation | ACT,GCT | T,A 580 | XP_011528646.1 | |
XM_017028920.1 | 1827 | Missense Mutation | ACT,GCT | T,A 679 | XP_016884409.1 |