Product Details

SNP ID
rs201476543
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:22548171 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCACTAAGCCAGACCATGCTGGGCC[A/G]CCCCAACTCACACAGCAACTCCCTG
Phenotype
MIM: 606021
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
PRAME PubMed Links

Gene Details

Gene
PRAME
Gene Name
preferentially expressed antigen in melanoma
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001291715.1 1951 Silent Mutation NP_001278644.1
NM_001291716.1 1951 Silent Mutation NP_001278645.1
NM_001291717.1 1951 Silent Mutation NP_001278646.1
NM_001291719.1 1951 Silent Mutation NP_001278648.1
NM_001318126.1 1951 Silent Mutation NP_001305055.1
NM_001318127.1 1951 Silent Mutation NP_001305056.1
NM_006115.4 1951 Silent Mutation NP_006106.1
NM_206953.2 1951 Silent Mutation NP_996836.1
NM_206954.2 1951 Silent Mutation NP_996837.1
NM_206955.2 1951 Silent Mutation NP_996838.1
NM_206956.2 1951 Silent Mutation NP_996839.1
XM_011530034.2 1951 Missense Mutation XP_011528336.1

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