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CAGAGACACAATGAGTGCTGAAGAG[A/G]GGAGACTTCCTAGGAAATGAAGAAG
Species: |
Human | ||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611034 | ||||||||||||||||||||||||||
Literature Links: |
SLC17A3 PubMed Links | ||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS - Not Available | Chinese - Not Available | JPT (Japanese)
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AFR - Not Available | Japanese - Not Available | CHB (Han Chinese)
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EUR - Not Available | |||||
AMR - Not Available |
SLC17A3 - solute carrier family 17 member 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001098486.1 | 1009 | Missense Mutation | CCC,CTC | P,L 378 | NP_001091956.1 | |
NM_006632.3 | 1009 | Missense Mutation | CCC,CTC | P,L 300 | NP_006623.2 |
Set Membership: |
HapMap |