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GGCCAAACATGTTGACTGCAGCAGA[C/T]AGGAAAAAGACATTCCTCCAACCAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611049 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC17A2 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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SLC17A2 - solute carrier family 17 member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001286123.1 | 1758 | Silent Mutation | CTA,CTG | L,L 446 | NP_001273052.1 | |
NM_001286125.1 | 1758 | UTR 3 | NP_001273054.1 | |||
NM_005835.3 | 1758 | Missense Mutation | TAT,TGT | Y,C 397 | NP_005826.1 | |
XM_005248784.2 | 1758 | Silent Mutation | CTA,CTG | L,L 446 | XP_005248841.1 | |
XM_006714949.3 | 1758 | Silent Mutation | CTA,CTG | L,L 446 | XP_006715012.1 | |
XM_006714950.2 | 1758 | Silent Mutation | CTA,CTG | L,L 423 | XP_006715013.1 | |
XM_006714951.1 | 1758 | UTR 3 | XP_006715014.1 | |||
XM_017010159.1 | 1758 | Silent Mutation | CTA,CTG | L,L 423 | XP_016865648.1 | |
XM_017010160.1 | 1758 | UTR 3 | XP_016865649.1 |