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GGCTTCTTGGGGAGGGACTGAGCCA[C/T]ATCTTGAAAGCTAGGAAGCGGGAGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608736 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC39A14 PubMed Links | ||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
---|---|---|---|---|---|---|---|---|
Global
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Caucasian
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CEPH (CEU) - Not Available | ||||||
EAS
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African American
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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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SLC39A14 - solute carrier family 39 member 14 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001128431.2 | Intron | NP_001121903.1 | ||||
NM_001135153.1 | Intron | NP_001128625.1 | ||||
NM_001135154.1 | Intron | NP_001128626.1 | ||||
NM_015359.4 | Intron | NP_056174.2 | ||||
XM_005273465.2 | Intron | XP_005273522.1 | ||||
XM_005273466.4 | Intron | XP_005273523.1 | ||||
XM_006716323.2 | Intron | XP_006716386.1 | ||||
XM_006716324.2 | Intron | XP_006716387.1 | ||||
XM_011544478.2 | Intron | XP_011542780.1 | ||||
XM_017013292.1 | Intron | XP_016868781.1 | ||||
XM_017013293.1 | Intron | XP_016868782.1 | ||||
XM_017013294.1 | Intron | XP_016868783.1 | ||||
XM_017013295.1 | Intron | XP_016868784.1 |
Set Membership: |
Validated |