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TGTTTCTTCTACTCAGCCGTGTTTT[A/T]TCTACTGAGACAGACAAACCCTCAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608734 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC39A12 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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SLC39A12 - solute carrier family 39 member 12 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145195.1 | 339 | Missense Mutation | TTA,TTT | L,F 22 | NP_001138667.1 | |
NM_001282733.1 | 339 | Missense Mutation | TTA,TTT | L,F 22 | NP_001269662.1 | |
NM_001282734.1 | 339 | Intron | NP_001269663.1 | |||
NM_152725.3 | 339 | Missense Mutation | TTA,TTT | L,F 22 | NP_689938.2 |