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TCCGTGATCCCACACTCATCAAAGA[C/T]CAGGTCCTGGAGGGTGGCAGAGGCT
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) - 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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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 | 1675 | Missense Mutation | ATC,GTC | I,V 384 | NP_001278644.1 | |
NM_001291716.1 | 1675 | Missense Mutation | ATC,GTC | I,V 384 | NP_001278645.1 | |
NM_001291717.1 | 1675 | Missense Mutation | ATC,GTC | I,V 368 | NP_001278646.1 | |
NM_001291719.1 | 1675 | Missense Mutation | ATC,GTC | I,V 368 | NP_001278648.1 | |
NM_001318126.1 | 1675 | Missense Mutation | ATC,GTC | I,V 368 | NP_001305055.1 | |
NM_001318127.1 | 1675 | Missense Mutation | ATC,GTC | I,V 368 | NP_001305056.1 | |
NM_006115.4 | 1675 | Missense Mutation | ATC,GTC | I,V 384 | NP_006106.1 | |
NM_206953.2 | 1675 | Missense Mutation | ATC,GTC | I,V 384 | NP_996836.1 | |
NM_206954.2 | 1675 | Missense Mutation | ATC,GTC | I,V 384 | NP_996837.1 | |
NM_206955.2 | 1675 | Missense Mutation | ATC,GTC | I,V 384 | NP_996838.1 | |
NM_206956.2 | 1675 | Missense Mutation | ATC,GTC | I,V 384 | NP_996839.1 | |
XM_011530034.2 | 1675 | Missense Mutation | ATC,GTC | I,V 368 | XP_011528336.1 |