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CCATGACCACGTAGACCATGGCACC[A/G]GCAGCAAAGGCCAGAGCGTAGGGCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 616508 | ||||||||||||||||||||
Literature Links: |
LINC00511 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 |
LINC00511 - long intergenic non-protein coding RNA 511 | ||||||
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There are no transcripts associated with this gene. |
SLC39A11 - solute carrier family 39 member 11 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001159770.1 | 988 | Silent Mutation | GCC,GCT | A,A 299 | NP_001153242.1 | |
NM_139177.3 | 988 | Silent Mutation | GCC,GCT | A,A 292 | NP_631916.2 | |
XM_005257134.3 | 988 | Silent Mutation | GCC,GCT | A,A 292 | XP_005257191.1 | |
XM_006721754.3 | 988 | Silent Mutation | GCC,GCT | A,A 299 | XP_006721817.1 | |
XM_006721755.2 | 988 | Silent Mutation | GCC,GCT | A,A 299 | XP_006721818.1 | |
XM_006721756.2 | 988 | Intron | XP_006721819.1 | |||
XM_006721757.2 | 988 | Silent Mutation | GCC,GCT | A,A 242 | XP_006721820.1 | |
XM_006721758.3 | 988 | Intron | XP_006721821.1 | |||
XM_006721759.1 | 988 | Intron | XP_006721822.1 | |||
XM_011524493.1 | 988 | Silent Mutation | GCC,GCT | A,A 299 | XP_011522795.1 | |
XM_011524494.2 | 988 | Silent Mutation | GCC,GCT | A,A 299 | XP_011522796.1 | |
XM_011524495.2 | 988 | Intron | XP_011522797.1 | |||
XM_011524496.2 | 988 | Intron | XP_011522798.1 | |||
XM_011524498.2 | 988 | Intron | XP_011522800.1 | |||
XM_017024330.1 | 988 | Silent Mutation | GCC,GCT | A,A 292 | XP_016879819.1 | |
XM_017024331.1 | 988 | Silent Mutation | GCC,GCT | A,A 292 | XP_016879820.1 | |
XM_017024332.1 | 988 | Silent Mutation | GCC,GCT | A,A 292 | XP_016879821.1 | |
XM_017024333.1 | 988 | Silent Mutation | GCC,GCT | A,A 249 | XP_016879822.1 | |
XM_017024334.1 | 988 | Silent Mutation | GCC,GCT | A,A 242 | XP_016879823.1 | |
XM_017024335.1 | 988 | Silent Mutation | GCC,GCT | A,A 235 | XP_016879824.1 | |
XM_017024336.1 | 988 | Silent Mutation | GCC,GCT | A,A 249 | XP_016879825.1 | |
XM_017024337.1 | 988 | Silent Mutation | GCC,GCT | A,A 249 | XP_016879826.1 | |
XM_017024338.1 | 988 | Intron | XP_016879827.1 | |||
XM_017024339.1 | 988 | Intron | XP_016879828.1 | |||
XM_017024340.1 | 988 | Intron | XP_016879829.1 | |||
XM_017024341.1 | 988 | Intron | XP_016879830.1 | |||
XM_017024342.1 | 988 | Intron | XP_016879831.1 |