Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 616526 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC38A11 PubMed Links | ||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
---|---|---|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | ||||||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | ||||||
SAS
|
Chinese - Not Available | JPT (Japanese)
|
||||||
AFR
|
Japanese - Not Available | CHB (Han Chinese)
|
||||||
EUR
|
||||||||
AMR
|
SLC38A11 - solute carrier family 38 member 11 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001199148.1 | Intron | NP_001186077.1 | ||||
NM_173512.2 | Intron | NP_775783.1 | ||||
XM_005246350.4 | Intron | XP_005246407.1 | ||||
XM_006712337.3 | Intron | XP_006712400.1 | ||||
XM_011510737.2 | Intron | XP_011509039.1 | ||||
XM_011510742.2 | Intron | XP_011509044.1 | ||||
XM_017003455.1 | Intron | XP_016858944.1 | ||||
XM_017003456.1 | Intron | XP_016858945.1 | ||||
XM_017003457.1 | Intron | XP_016858946.1 | ||||
XM_017003458.1 | Intron | XP_016858947.1 | ||||
XM_017003459.1 | Intron | XP_016858948.1 | ||||
XM_017003460.1 | Intron | XP_016858949.1 | ||||
XM_017003461.1 | Intron | XP_016858950.1 | ||||
XM_017003462.1 | Intron | XP_016858951.1 | ||||
XM_017003463.1 | Intron | XP_016858952.1 | ||||
XM_017003464.1 | Intron | XP_016858953.1 | ||||
XM_017003465.1 | Intron | XP_016858954.1 |
Set Membership: |
HapMap |