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CTTGAGTATTTGTAATAGCCATGAC[A/G]AATCCAAAAACCATCACCACAGCAC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 616526 | ||||||||||||||||||||
Literature Links: |
SLC38A11 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 |
SLC38A11 - solute carrier family 38 member 11 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001199148.1 | 1716 | Silent Mutation | TTC,TTT | F,F 357 | NP_001186077.1 | |
NM_173512.2 | 1716 | Silent Mutation | TTC,TTT | F,F 335 | NP_775783.1 | |
XM_005246350.4 | 1716 | Silent Mutation | TTC,TTT | F,F 413 | XP_005246407.1 | |
XM_006712337.3 | 1716 | Silent Mutation | TTC,TTT | F,F 359 | XP_006712400.1 | |
XM_011510737.2 | 1716 | Silent Mutation | TTC,TTT | F,F 391 | XP_011509039.1 | |
XM_011510742.2 | 1716 | Silent Mutation | TTC,TTT | F,F 218 | XP_011509044.1 | |
XM_017003455.1 | 1716 | Silent Mutation | TTC,TTT | F,F 439 | XP_016858944.1 | |
XM_017003456.1 | 1716 | Silent Mutation | TTC,TTT | F,F 417 | XP_016858945.1 | |
XM_017003457.1 | 1716 | Silent Mutation | TTC,TTT | F,F 414 | XP_016858946.1 | |
XM_017003458.1 | 1716 | Silent Mutation | TTC,TTT | F,F 383 | XP_016858947.1 | |
XM_017003459.1 | 1716 | Silent Mutation | TTC,TTT | F,F 361 | XP_016858948.1 | |
XM_017003460.1 | 1716 | Intron | XP_016858949.1 | |||
XM_017003461.1 | 1716 | Intron | XP_016858950.1 | |||
XM_017003462.1 | 1716 | Intron | XP_016858951.1 | |||
XM_017003463.1 | 1716 | Silent Mutation | TTC,TTT | F,F 291 | XP_016858952.1 | |
XM_017003464.1 | 1716 | Silent Mutation | TTC,TTT | F,F 244 | XP_016858953.1 | |
XM_017003465.1 | 1716 | Silent Mutation | TTC,TTT | F,F 244 | XP_016858954.1 |