Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606021 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
PRAME 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)
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SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | ||||||
AFR
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Japanese - Not Available | JPT (Japanese)
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EUR
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AMR
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PRAME - preferentially expressed antigen in melanoma | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001291715.1 | 2052 | Silent Mutation | AAC,AAT | N,N 509 | NP_001278644.1 | |
NM_001291716.1 | 2052 | Silent Mutation | AAC,AAT | N,N 509 | NP_001278645.1 | |
NM_001291717.1 | 2052 | Silent Mutation | AAC,AAT | N,N 493 | NP_001278646.1 | |
NM_001291719.1 | 2052 | Silent Mutation | AAC,AAT | N,N 493 | NP_001278648.1 | |
NM_001318126.1 | 2052 | Silent Mutation | AAC,AAT | N,N 493 | NP_001305055.1 | |
NM_001318127.1 | 2052 | Silent Mutation | AAC,AAT | N,N 493 | NP_001305056.1 | |
NM_006115.4 | 2052 | Silent Mutation | AAC,AAT | N,N 509 | NP_006106.1 | |
NM_206953.2 | 2052 | Silent Mutation | AAC,AAT | N,N 509 | NP_996836.1 | |
NM_206954.2 | 2052 | Silent Mutation | AAC,AAT | N,N 509 | NP_996837.1 | |
NM_206955.2 | 2052 | Silent Mutation | AAC,AAT | N,N 509 | NP_996838.1 | |
NM_206956.2 | 2052 | Silent Mutation | AAC,AAT | N,N 509 | NP_996839.1 | |
XM_011530034.2 | 2052 | Silent Mutation | AAC,AAT | N,N 493 | XP_011528336.1 |