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AACATCACAGGGAGGTCTCCTGGAG[C/G]ATGCAGGTGGAGCTGCTCCCCTGAT
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 - 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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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 | 2177 | Missense Mutation | ATC,ATG | I,M 629 | NP_066918.2 | |
XM_006712128.1 | 2177 | Missense Mutation | ATC,ATG | I,M 629 | XP_006712191.1 | |
XM_006712129.1 | 2177 | Missense Mutation | ATC,ATG | I,M 629 | XP_006712192.1 | |
XM_006712130.1 | 2177 | Missense Mutation | ATC,ATG | I,M 629 | XP_006712193.1 | |
XM_011533146.2 | 2177 | Missense Mutation | ATC,ATG | I,M 406 | XP_011531448.1 | |
XM_017005216.1 | 2177 | Missense Mutation | ATC,ATG | I,M 420 | XP_016860705.1 |