Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTCTCCAGGGGGACAGGATACAGCA[C/G]GTGGGTCAGATTGCTCAGCCCGATG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 606021 | ||||||||||||||||||||
Literature Links: |
PRAME PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
PRAME - preferentially expressed antigen in melanoma | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001291715.1 | 1840 | Missense Mutation | CTG,GTG | L,V 439 | NP_001278644.1 | |
NM_001291716.1 | 1840 | Missense Mutation | CTG,GTG | L,V 439 | NP_001278645.1 | |
NM_001291717.1 | 1840 | Missense Mutation | CTG,GTG | L,V 423 | NP_001278646.1 | |
NM_001291719.1 | 1840 | Missense Mutation | CTG,GTG | L,V 423 | NP_001278648.1 | |
NM_001318126.1 | 1840 | Missense Mutation | CTG,GTG | L,V 423 | NP_001305055.1 | |
NM_001318127.1 | 1840 | Missense Mutation | CTG,GTG | L,V 423 | NP_001305056.1 | |
NM_006115.4 | 1840 | Missense Mutation | CTG,GTG | L,V 439 | NP_006106.1 | |
NM_206953.2 | 1840 | Missense Mutation | CTG,GTG | L,V 439 | NP_996836.1 | |
NM_206954.2 | 1840 | Missense Mutation | CTG,GTG | L,V 439 | NP_996837.1 | |
NM_206955.2 | 1840 | Missense Mutation | CTG,GTG | L,V 439 | NP_996838.1 | |
NM_206956.2 | 1840 | Missense Mutation | CTG,GTG | L,V 439 | NP_996839.1 | |
XM_011530034.2 | 1840 | Missense Mutation | CTG,GTG | L,V 423 | XP_011528336.1 |