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CGTTCCAGCCATTGCCACTAAATTC[C/T]GCGCAGTCTTCCTCCCCAACGTTGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604672 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CD209 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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CD209 - CD209 molecule | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001144893.1 | 755 | Silent Mutation | GCA,GCG | A,A 221 | NP_001138365.1 | |
NM_001144894.1 | 755 | Silent Mutation | GCA,GCG | A,A 313 | NP_001138366.1 | |
NM_001144895.1 | 755 | Silent Mutation | GCA,GCG | A,A 265 | NP_001138367.1 | |
NM_001144896.1 | 755 | Silent Mutation | GCA,GCG | A,A 333 | NP_001138368.1 | |
NM_001144897.1 | 755 | Silent Mutation | GCA,GCG | A,A 351 | NP_001138369.1 | |
NM_001144899.1 | 755 | Silent Mutation | GCA,GCG | A,A 196 | NP_001138371.1 | |
NM_021155.3 | 755 | Silent Mutation | GCA,GCG | A,A 357 | NP_066978.1 | |
XM_005272472.4 | 755 | Silent Mutation | GCA,GCG | A,A 219 | XP_005272529.1 |