Product Details
- SNP ID
-
rs13604
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.22:22548070 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- AGCATTTGATATGTGCACCCAGCTA[A/G]TTAGGCATGAAACAGGGGCACAGGA
- 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 |
2052 |
Silent Mutation |
AAC,AAT |
N509N |
NP_001278644.1 |
| NM_001291716.1 |
2052 |
Silent Mutation |
AAC,AAT |
N509N |
NP_001278645.1 |
| NM_001291717.1 |
2052 |
Silent Mutation |
AAC,AAT |
N493N |
NP_001278646.1 |
| NM_001291719.1 |
2052 |
Silent Mutation |
AAC,AAT |
N493N |
NP_001278648.1 |
| NM_001318126.1 |
2052 |
Silent Mutation |
AAC,AAT |
N493N |
NP_001305055.1 |
| NM_001318127.1 |
2052 |
Silent Mutation |
AAC,AAT |
N493N |
NP_001305056.1 |
| NM_006115.4 |
2052 |
Silent Mutation |
AAC,AAT |
N509N |
NP_006106.1 |
| NM_206953.2 |
2052 |
Silent Mutation |
AAC,AAT |
N509N |
NP_996836.1 |
| NM_206954.2 |
2052 |
Silent Mutation |
AAC,AAT |
N509N |
NP_996837.1 |
| NM_206955.2 |
2052 |
Silent Mutation |
AAC,AAT |
N509N |
NP_996838.1 |
| NM_206956.2 |
2052 |
Silent Mutation |
AAC,AAT |
N509N |
NP_996839.1 |
| XM_011530034.2 |
2052 |
Silent Mutation |
AAC,AAT |
N493N |
XP_011528336.1 |
View Full Product Details