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CCCAACCATTCCTGGAATAGTGGCA[A/G]ATGTATTTGTGATGCCCAGGAGGAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604322 | ||||||||||||||||||||
Literature Links: |
SLC17A5 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
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 | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
SLC17A5 - solute carrier family 17 member 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_012434.4 | 1233 | Missense Mutation | TCT,TTT | S,F 432 | NP_036566.1 | |
XM_005248710.3 | 1233 | Missense Mutation | TCT,TTT | S,F 415 | XP_005248767.1 | |
XM_005248711.2 | 1233 | Missense Mutation | TCT,TTT | S,F 366 | XP_005248768.1 | |
XM_011535750.2 | 1233 | Silent Mutation | CTG,TTG | L,L 383 | XP_011534052.1 | |
XM_017010730.1 | 1233 | Missense Mutation | TCT,TTT | S,F 301 | XP_016866219.1 | |
XM_017010731.1 | 1233 | Missense Mutation | TCT,TTT | S,F 301 | XP_016866220.1 |