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GCAGCTGGAGAATCCAAACCGGGAG[C/T]AGAGCCGGGATGAGGCTTCAGCCAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602878 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC30A3 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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SLC30A3 - solute carrier family 30 member 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001318949.1 | 1113 | Missense Mutation | TAC,TGC | Y,C 352 | NP_001305878.1 | |
NM_001318950.1 | 1113 | Missense Mutation | TAC,TGC | Y,C 344 | NP_001305879.1 | |
NM_001318951.1 | 1113 | Missense Mutation | TAC,TGC | Y,C 344 | NP_001305880.1 | |
NM_003459.4 | 1113 | Missense Mutation | TAC,TGC | Y,C 357 | NP_003450.2 | |
XM_005264547.1 | 1113 | Missense Mutation | ACT,GCT | T,A 306 | XP_005264604.1 | |
XM_005264548.3 | 1113 | Missense Mutation | ACT,GCT | T,A 301 | XP_005264605.1 | |
XM_006712100.2 | 1113 | Missense Mutation | ACT,GCT | T,A 257 | XP_006712163.1 | |
XM_011533102.2 | 1113 | Missense Mutation | TAC,TGC | Y,C 284 | XP_011531404.1 | |
XM_011533103.2 | 1113 | Missense Mutation | TAC,TGC | Y,C 243 | XP_011531405.1 | |
XM_017004873.1 | 1113 | Missense Mutation | ACT,GCT | T,A 293 | XP_016860362.1 | |
XM_017004874.1 | 1113 | Missense Mutation | ACT,GCT | T,A 293 | XP_016860363.1 | |
XM_017004875.1 | 1113 | Missense Mutation | ACT,GCT | T,A 284 | XP_016860364.1 |