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CCCGGACTCCTGGCACCGACAACAG[C/T]GTATCCCGCACAGGTTCGAACCCCA
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 |
---|---|---|
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 |
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 | 967 | Silent Mutation | ACA,ACG | T,T 303 | NP_001305878.1 | |
NM_001318950.1 | 967 | Silent Mutation | ACA,ACG | T,T 295 | NP_001305879.1 | |
NM_001318951.1 | 967 | Silent Mutation | ACA,ACG | T,T 295 | NP_001305880.1 | |
NM_003459.4 | 967 | Silent Mutation | ACA,ACG | T,T 308 | NP_003450.2 | |
XM_005264547.1 | 967 | Missense Mutation | CAC,CGC | H,R 257 | XP_005264604.1 | |
XM_005264548.3 | 967 | Missense Mutation | CAC,CGC | H,R 252 | XP_005264605.1 | |
XM_006712100.2 | 967 | Missense Mutation | CAC,CGC | H,R 208 | XP_006712163.1 | |
XM_011533102.2 | 967 | Silent Mutation | ACA,ACG | T,T 235 | XP_011531404.1 | |
XM_011533103.2 | 967 | Silent Mutation | ACA,ACG | T,T 194 | XP_011531405.1 | |
XM_017004873.1 | 967 | Missense Mutation | CAC,CGC | H,R 244 | XP_016860362.1 | |
XM_017004874.1 | 967 | Missense Mutation | CAC,CGC | H,R 244 | XP_016860363.1 | |
XM_017004875.1 | 967 | Missense Mutation | CAC,CGC | H,R 235 | XP_016860364.1 |