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Search Thermo Fisher Scientific
CCCTCCTTGCAGTACCTGGAGATGC[A/G]CTTCAGCCGCGCAGTGCGGCTCTGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601843 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC5A5 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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SLC5A5 - solute carrier family 5 member 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000453.2 | 1297 | Missense Mutation | CAC,CGC | H,R 124 | NP_000444.1 | |
XM_011528192.2 | 1297 | Missense Mutation | CAC,CGC | H,R 124 | XP_011526494.1 | |
XM_011528193.2 | 1297 | Missense Mutation | CAC,CGC | H,R 35 | XP_011526495.1 | |
XM_011528194.2 | 1297 | Missense Mutation | CAC,CGC | H,R 2 | XP_011526496.1 | |
XM_017027158.1 | 1297 | Missense Mutation | CAC,CGC | H,R 35 | XP_016882647.1 |