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GAGGACCCATCATGGCCAGAAACAG[C/T]GGCTGCTGCAGAAGGGCGAAGAGCG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610791 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC43A2 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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SLC43A2 - solute carrier family 43 member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001284498.1 | 1642 | Silent Mutation | CCA,CCG | P,P 505 | NP_001271427.1 | |
NM_001284499.1 | 1642 | Silent Mutation | CCA,CCG | P,P 364 | NP_001271428.1 | |
NM_001321364.1 | 1642 | Silent Mutation | CCA,CCG | P,P 505 | NP_001308293.1 | |
NM_001321365.1 | 1642 | Silent Mutation | CCA,CCG | P,P 505 | NP_001308294.1 | |
NM_152346.2 | 1642 | Silent Mutation | CCA,CCG | P,P 501 | NP_689559.1 | |
XM_017024177.1 | 1642 | Silent Mutation | CCA,CCG | P,P 501 | XP_016879666.1 | |
XM_017024178.1 | 1642 | Silent Mutation | CCA,CCG | P,P 501 | XP_016879667.1 | |
XM_017024179.1 | 1642 | Silent Mutation | CCA,CCG | P,P 468 | XP_016879668.1 |