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AGCATGACACAAGACATAATCTTAT[C/T]GGAGTGTGTCCTTGGTTCTTCAGAC
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 | |||
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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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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 | 1657 | Missense Mutation | AAT,GAT | N,D 338 | NP_001186077.1 | |
NM_173512.2 | 1657 | Missense Mutation | AAT,GAT | N,D 316 | NP_775783.1 | |
XM_005246350.4 | 1657 | Missense Mutation | AAT,GAT | N,D 394 | XP_005246407.1 | |
XM_006712337.3 | 1657 | Missense Mutation | AAT,GAT | N,D 340 | XP_006712400.1 | |
XM_011510737.2 | 1657 | Missense Mutation | AAT,GAT | N,D 372 | XP_011509039.1 | |
XM_011510742.2 | 1657 | Missense Mutation | AAT,GAT | N,D 199 | XP_011509044.1 | |
XM_017003455.1 | 1657 | Missense Mutation | AAT,GAT | N,D 420 | XP_016858944.1 | |
XM_017003456.1 | 1657 | Missense Mutation | AAT,GAT | N,D 398 | XP_016858945.1 | |
XM_017003457.1 | 1657 | Missense Mutation | AAT,GAT | N,D 395 | XP_016858946.1 | |
XM_017003458.1 | 1657 | Missense Mutation | AAT,GAT | N,D 364 | XP_016858947.1 | |
XM_017003459.1 | 1657 | Missense Mutation | AAT,GAT | N,D 342 | XP_016858948.1 | |
XM_017003460.1 | 1657 | Intron | XP_016858949.1 | |||
XM_017003461.1 | 1657 | Intron | XP_016858950.1 | |||
XM_017003462.1 | 1657 | Intron | XP_016858951.1 | |||
XM_017003463.1 | 1657 | Missense Mutation | AAT,GAT | N,D 272 | XP_016858952.1 | |
XM_017003464.1 | 1657 | Missense Mutation | AAT,GAT | N,D 225 | XP_016858953.1 | |
XM_017003465.1 | 1657 | Missense Mutation | AAT,GAT | N,D 225 | XP_016858954.1 |