Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604024 | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC5A6 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
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CEPH (CEU) - Not Available | |||||||||
EAS
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African American
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YRI (Yoruba)
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SAS
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Japanese
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CHB (Han Chinese) - Not Available | |||||||||
AFR
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Chinese
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JPT (Japanese) - Not Available | |||||||||
EUR
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AMR
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SLC5A6 - solute carrier family 5 member 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_021095.2 | 1765 | Missense Mutation | AAC,AGC | N,S 492 | NP_066918.2 | |
XM_006712128.1 | 1765 | Missense Mutation | AAC,AGC | N,S 492 | XP_006712191.1 | |
XM_006712129.1 | 1765 | Missense Mutation | AAC,AGC | N,S 492 | XP_006712192.1 | |
XM_006712130.1 | 1765 | Missense Mutation | AAC,AGC | N,S 492 | XP_006712193.1 | |
XM_011533146.2 | 1765 | Missense Mutation | AAC,AGC | N,S 269 | XP_011531448.1 | |
XM_017005216.1 | 1765 | Missense Mutation | AAC,AGC | N,S 283 | XP_016860705.1 |
Set Membership: |
HapMap DME Validated Inventoried |