Product Details
- SNP ID
-
rs146074761
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.8:22025521 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- AGAGCTGCAGGCTGTTGCTTCATAC[G/T]GTAGGTGTTCCCAAAAGAGGGGAGG
- Phenotype
-
MIM: 608073
- Polymorphism
- G/T, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
NPM2
PubMed Links
Gene Details
- Gene
- NPM2
- Gene Name
- nucleophosmin/nucleoplasmin 2
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001286680.1 |
798 |
Silent Mutation |
ACG,ACT |
T48T |
NP_001273609.1 |
| NM_001286681.1 |
798 |
Silent Mutation |
ACG,ACT |
T48T |
NP_001273610.1 |
| NM_182795.1 |
798 |
Silent Mutation |
ACG,ACT |
T48T |
NP_877724.1 |
| XM_011544360.2 |
798 |
Silent Mutation |
ACG,ACT |
T123T |
XP_011542662.1 |
| XM_011544362.2 |
798 |
Silent Mutation |
ACG,ACT |
T48T |
XP_011542664.1 |
| XM_011544363.2 |
798 |
Silent Mutation |
ACG,ACT |
T48T |
XP_011542665.1 |
| XM_011544364.2 |
798 |
UTR 5 |
|
|
XP_011542666.1 |
| XM_017012947.1 |
798 |
Silent Mutation |
ACG,ACT |
T123T |
XP_016868436.1 |
| XM_017012948.1 |
798 |
Silent Mutation |
ACG,ACT |
T48T |
XP_016868437.1 |
| XM_017012949.1 |
798 |
Silent Mutation |
ACG,ACT |
T48T |
XP_016868438.1 |
| XM_017012950.1 |
798 |
Silent Mutation |
ACG,ACT |
T48T |
XP_016868439.1 |
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